Your gut microbes might encourage criminal behavior

A few years ago, a Belgian man in his 30s drove into a lamppost. Twice. Local authorities found that his blood alcohol level was four times the legal limit. Over the space of a few years, the man was apprehended for drunk driving three times. And on all three occasions, he insisted he hadn’t been drinking.

He was telling the truth. A doctor later diagnosed auto-brewery syndrome—a rare condition in which the body makes its own alcohol. Microbes living inside the man’s body were fermenting the carbohydrates in his diet to create ethanol. Last year, he was acquitted of drunk driving.

His case, along with several other scientific studies, raises a fascinating question for microbiology, neuroscience, and the law: How much of our behavior can we blame on our microbes?

Each of us hosts vast communities of tiny bacteria, archaea (which are a bit like bacteria), fungi, and even viruses all over our bodies. The largest collection resides in our guts, which play home to trillions of them. You have more microbial cells than human cells in your body. In some ways, we’re more microbe than human.

Microbiologists are still getting to grips with what all these microbes do. Some seem to help us break down food. Others produce chemicals that are important for our health in some way. But the picture is extremely complicated, partly because of the myriad ways microbes can interact with each other.

But they also interact with the human nervous system. Microbes can produce compounds that affect the way neurons work. They also influence the functioning of the immune system, which can have knock-on effects on the brain. And they seem to be able to communicate with the brain via the vagus nerve.

If microbes can influence our brains, could they also explain some of our behavior, including the criminal sort? Some microbiologists think so, at least in theory. “Microbes control us more than we think they do,” says Emma Allen-Vercoe, a microbiologist at the University of Guelph in Canada.

Researchers have come up with a name for applications of microbiology to criminal law: the legalome. A better understanding of how microbes influence our behavior could not only affect legal proceedings but also shape crime prevention and rehabilitation efforts, argue Susan Prescott, a pediatrician and immunologist at the University of Western Australia, and her colleagues.

“For the person unaware that they have auto-brewery syndrome, we can argue that microbes are like a marionettist pulling the strings in what would otherwise be labeled as criminal behavior,” says Prescott.

Auto-brewery syndrome is a fairly straightforward example (it has been involved in the acquittal of at least two people so far), but other brain-microbe relationships are likely to be more complicated. We do know a little about one microbe that seems to influence behavior: Toxoplasmosis gondii, a parasite that reproduces in cats and spreads to other animals via cat feces.

The parasite is best known for changing the behavior of rodents in ways that make them easier prey—an infection seems to make mice permanently lose their fear of cats. Research in humans is nowhere near conclusive, but some studies have linked infections with the parasite to personality changes, increased aggression, and impulsivity.

“That’s an example of microbiology that we know affects the brain and could potentially affect the legal standpoint of someone who’s being tried for a crime,” says Allen-Vercoe. “They might say ‘My microbes made me do it,’ and I might believe them.”

There’s more evidence linking gut microbes to behavior in mice, which are some of the most well-studied creatures. One study involved fecal transplants—a procedure that involves inserting fecal matter from one animal into the intestines of another. Because feces contain so much gut bacteria, fecal transplants can go some way to swap out a gut microbiome. (Humans are doing this too—and it seems to be a remarkably effective way to treat persistent C. difficile infections in people.)

Back in 2013, scientists at McMaster University in Canada performed fecal transplants between two strains of mice, one that is known for being timid and another that tends to be rather gregarious. This swapping of gut microbes also seemed to swap their behavior—the timid mice became more gregarious, and vice versa.

Microbiologists have since held up this study as one of the clearest demonstrations of how changing gut microbes can change behavior—at least in mice. “But the question is: How much do they control you, and how much is the human part of you able to overcome that control?” says Allen-Vercoe. “And that’s a really tough question to answer.”

After all, our gut microbiomes, though relatively stable, can change. Your diet, exercise routine, environment, and even the people you live with can shape the communities of microbes that live on and in you. And the ways these communities shift and influence behavior might be slightly different for everyone. Pinning down precise links between certain microbes and criminal behaviors will be extremely difficult, if not impossible. 

“I don’t think you’re going to be able to take someone’s microbiome and say ‘Oh, look—you’ve got bug X, and that means you’re a serial killer,” says Allen-Vercoe.

Either way, Prescott hopes that advances in microbiology and metabolomics might help us better understand the links between microbes, the chemicals they produce, and criminal behaviors—and potentially even treat those behaviors.

“We could get to a place where microbial interventions are a part of therapeutic programming,” she says.

This article first appeared in The Checkup, MIT Technology Review’s weekly biotech newsletter. To receive it in your inbox every Thursday, and read articles like this first, sign up here.

Bryan Johnson wants to start a new religion in which “the body is God”

Bryan Johnson is on a mission to not die. The 47-year-old multimillionaire has already applied his slogan “Don’t Die” to events, merchandise, and a Netflix documentary. Now he’s founding a Don’t Die religion.

Johnson, who famously spends millions of dollars on scans, tests, supplements, and a lifestyle routine designed to slow or reverse the aging process, has enjoyed extensive media coverage, and a huge social media following. For many people, he has become the face of the longevity field.

I sat down with Johnson at an event for people interested in longevity in Berkeley, California, in late April. We spoke on the sidelines after lunch (conference plastic-lidded container meal for me; what seemed to be a plastic-free, compostable box of chicken and vegetables for him), and he sat with an impeccable posture, his expression neutral. 

Earlier that morning, Johnson, in worn trainers and the kind of hoodie that is almost certainly deceptively expensive, had told the audience about what he saw as the end of humanity. Specifically, he was worried about AI—that we face an “event horizon,” a point at which superintelligent AI escapes human understanding and control. He had come to Berkeley to persuade people who are interested in longevity to focus their efforts on AI. 

It is this particular concern that ultimately underpins his Don’t Die mission. First, humans must embrace the Don’t Die ideology. Then we must ensure AI is aligned with preserving human existence. Were it not for AI, he says, he wouldn’t be doing any of his anti-death activities and regimens. “I am convinced that we are at an existential moment as a species,” says Johnson, who was raised Mormon but has since left the church. Solving aging will take decades, he says—we’ll survive that long only if we make sure that AI is aligned with human survival. 

The following Q&A has been lightly edited for length and clarity.

Why are you creating a new religion?

We’re in this new phase where [because of advances in AI] we’re trying to reimagine what it means to be human. It requires imagination and creativity and open-mindedness, and that’s a big ask. Approaching that conversation as a community, or a lifestyle, doesn’t carry enough weight or power. Religions have proven, over the past several thousand years, to be the most efficacious form to organize human efforts. It’s just a tried-and-true methodology. 

How do you go about founding a new religion?

It’s a good question. If you look at historical [examples], Buddha went through his own self-exploratory process and came up with a framework. And Muhammad had a story. Jesus had an origin story … You might even say Satoshi [Nakamoto, the mysterious creator of bitcoin] is like [the founder of] a modern-day religion, [launched] with the white paper. Adam Smith launched capitalism with his book. The question is: What is a modern-day religion, and how does it convince? It’s an open question for me. I don’t know yet.

Your goal is to align AI with Don’t Die—or, in other words, ensure that AI models prioritize and protect human life. How will you do that?

I’m talking to a lot of AI researchers about this. Communities of AIs could be instilled with values of conflict resolution that do not end in the death of a human. Or an AI. Or the planet.

Would you say that Don’t Die is “your” religion?

No, I think it’s humanity’s religion. It’s different from other religions, which are very founder-centric. I think this is going to be decentralized, and it will be something that everybody can make their own.

So there’s no God?

We’re playing with the idea that the body is God. We’ve been experimenting with this format of a Don’t Die fam, where eight to 12 people get together on a weekly basis. It’s patterned off of other groups like Alcoholics Anonymous. We structure an opening ritual. We have a mantra. And then there’s a part where people apologize to their body for something they’ve done that has inflicted harm upon themselves. 

It’s reframing our relationship to body and to mind. It is also a way for people to have deep friendships, to explore emotionally vulnerable topics, and to support each other in health practices.

What we’re really trying to say is: Existence is the virtue. Existence is the objective. If someone believes in God, that’s fine. People can be Christian and do this; they can be Muslim and do this. Don’t Die is a “yes, and” to all groups.

So it’s a different way of thinking about religion?

Yeah. Right now, religion doesn’t hold the highest status in society. A lot of people look down on it in some way. I think as AI progresses, it’s going to create additional questions on who we are: What is our identity? What do we believe about our existence in the future? People are going to want some kind of framework that helps them make sense of the moment. So I think there’s going to be a shift toward religion in the coming years. People might say that [founding a religion now] is kind of a weird move, and that [religion] turns people off. But I think that’s fine. I think we’re ahead.

Does the religion incorporate, or make reference to, AI in any way?

Yeah. AI is going to be omnipresent. And this is why we’ve been contemplating “the body is God.” Over the past couple of years … I’ve been testing the hypothesis that if I get a whole bunch of data about my body, and I give it to an algorithm, and feed that algorithm updates with scientific evidence, then it would eventually do a better job than a doctor. So I gave myself over to an algorithm. 

It really is in my best interest to let it tell me what to eat, tell me when to sleep and exercise, because it would do a better job of making me happy. Instead of my mind haphazardly deciding what it wants to eat based on how it feels in the moment, the body is elevated to a position of authority. AI is going to be omnipresent and built into our everyday activities. Just like it autocompletes our texts, it will be able to autocomplete our thoughts.

Might some people interpret that as AI being God?

Potentially. I would be hesitant to try to define [someone else’s] God. The thing we want to align upon is that none of us want to die right now. We’re attempting to make Don’t Die the world’s most influential ideology in the next 18 months.

The US has approved CRISPR pigs for food

Most pigs in the US are confined to factory farms where they can be afflicted by a nasty respiratory virus that kills piglets. The illness is called porcine reproductive and respiratory syndrome, or PRRS.

A few years ago, a British company called Genus set out to design pigs immune to this germ using CRISPR gene editing. Not only did they succeed, but its pigs are now poised to enter the food chain following approval of the animals this week by the U.S. Food and Drug Administration.

The pigs will join a very short list of gene-modified animals that you can eat. It’s a short list because such animals are expensive to create, face regulatory barriers, and don’t always pay off. For instance, the US took about 20 years to approve a transgenic salmon with an extra gene that let it grow faster. But by early this year its creator, AquaBounty, had sold off all its fish farms and had only four employees—none of them selling fish.

Regulations have eased since then, especially around gene editing, which tinkers with an animal’s own DNA rather than adding to it from another species, as is the case with the salmon and many GMO crops.

What’s certain is that the pig project was technically impressive and scientifically clever. Genus edited pig embryos to remove the receptor that the PRRS virus uses to enter cells. No receptor means no infection.

According to Matt Culbertson, chief operating office of the Pig Improvement Company, a Genus subsidiary, the pigs appear entirely immune to more than 99% of the known versions of the PRRS virus, although there is one rare subtype that may break through the protection.

This project is scientifically similar to the work that led to the infamous CRISPR babies born in China in 2018. In that case a scientist named He Jiankui edited twin girls to be resistant to HIV, also by trying to remove a receptor gene when they were just embryos in a dish.

That experiment on humans was widely decried as misguided. But pigs are a different story. The ethical concerns about experimenting are less serious, and the benefits of changing the genomes can be measured in dollars and cents. It’s going to save a lot of money if pigs are immune to the PRRS virus, which spreads quite easily, causing losses of $300 million a year or more in the US alone.

Globally, people get animal protein mostly from chickens, with pigs and cattle in second and third place. A 2023 report estimated that pigs account for 34% of all meat that’s eaten. Of the billion pigs in the world, about half are in China; the US comes in a distant second, with 80 million.

Recently, there’s been a lot of fairly silly news about genetically modified animals. A company called Colossal Biosciences used gene editing to modify wolves in ways it claimed made them resemble an extinct species, the dire wolf. And then there’s the L.A. Project, an effort run by biohackers who say they’ll make glow-in-the-dark rabbits and have a stretch goal of creating a horse with a horn—that’s right, a unicorn.

Both those projects are more about showmanship than usefulness. But they’re demonstrations of the growing power scientists have to modify mammals, thanks principally to new gene-editing tools combined with DNA sequencing that lets them peer into animals’ DNA.

Stopping viruses is a much better use of CRISPR. And research is ongoing to make pigs—as well as other livestock—invulnerable to other infections, including African swine fever and influenza. While PRRS doesn’t infect humans, pig and bird flus can. But if herds and flocks could be changed to resist those infections, that could cut the chances of the type of spillover that can occasionally cause dangerous pandemics.  

There’s a chance the Genus pigs could turn out to be the most financially valuable genetically modified animal ever created—the first CRISPR hit product to reach the food system. After the approval, the company’s stock value jumped up by a couple of hundred million dollars on the London Stock Exchange.

But there is still a way to go before gene-edited bacon appears on shelves in the US. Before it makes its sales pitch to pig farms, Genus says, it needs to also gain approval in Mexico, Canada, Japan and China which are big export markets for American pork.

Culbertson says gene-edited pork could appear in the US market sometime next year. He says the company does not think pork chops or other meat will need to carry any label identifying it as bioengineered. “We aren’t aware of any labelling requirement,” Culbertson says.

This article is from The Checkup, MIT Technology Review’s weekly health and biotech newsletter. To receive it in your inbox every Thursday, sign up here.

Longevity clinics around the world are selling unproven treatments

The quest for long, healthy life—and even immortality—is probably almost as old as humans are, but it’s never been hotter than it is right now. Today my newsfeed is full of claims about diets, exercise routines, and supplements that will help me live longer.

A lot of it is marketing fluff, of course. It should be fairly obvious that a healthy, plant-rich diet and moderate exercise will help keep you in good shape. And no drugs or supplements have yet been proved to extend human lifespan.

The growing field of longevity medicine is apparently aiming for something in between these two ends of the wellness spectrum. By combining the established tools of clinical medicine (think blood tests and scans) with some more experimental ones (tests that measure your biological age), these clinics promise to help their clients improve their health and longevity.

But a survey of longevity clinics around the world, carried out by an organization that publishes updates and research on the industry, is revealing a messier picture. In reality, these clinics—most of which cater only to the very wealthy—vary wildly in their offerings.

Today, the number of longevity clinics is thought to be somewhere in the hundreds. The proponents of these clinics say they represent the future of medicine. “We can write new rules on how we treat patients,” Eric Verdin, who directs the Buck Institute for Research on Aging, said at a professional meeting last year.

Phil Newman, who runs Longevity.Technology, a company that tracks the longevity industry, says he knows of 320 longevity clinics operating around the world. Some operate multiple centers on an international scale, while others involve a single “practitioner” incorporating some element of “longevity” into the treatments offered, he says. To get a better idea of what these offerings might be, Newman and his colleagues conducted a survey of 82 clinics around the world, including the US, Australia, Brazil, and multiple countries in Europe and Asia.

Some of the results are not all that surprising. Three-quarters of the clinics said that most of their clients were Gen Xers, aged between 44 and 59. This makes sense—anecdotally, it’s around this age that many people start to feel the effects of aging. And research suggests that waves of molecular changes associated with aging hit us in our 40s and again in our 60s. (Longevity influencers Bryan Johnson, Andrew Huberman, and Peter Attia all fall into this age group too.)

And I wasn’t surprised to see that plenty of clinics are offering aesthetic treatments, focusing more on how old their clients look. Of the clinics surveyed, 28% said they offered Botox injections, 35% offered hair loss treatments, and 38% offered “facial rejuvenation procedures.”  “The distinction between longevity medicine and aesthetic medicine remains blurred,” Andrea Maier of the National University of Singapore, and cofounder of a private longevity clinic, wrote in a commentary on the report.

Maier is also former president of the Healthy Longevity Medicine Society, an organization that was set up with the aim of establishing clinical standards and credibility for longevity clinics. Other results from the survey underline how much of a challenge this will be; many clinics are still offering unproven treatments. Over a third of the clinics said they offered stem-cell treatments, for example. There is no evidence that those treatments will help people live longer—and they are not without risk, either.

I was a little surprised to see that most of the clinics are also offering prescription medicines off label. In other words, drugs that have been approved for specific medical issues are apparently being prescribed for aging instead. This is also not without risks—all medicines have side effects. And, again, none of them have been proved to slow or reverse human aging.

And these prescriptions are coming from certified medical doctors. More than 80% of clinics reported that their practice was overseen by a medical doctor with more than 10 years of clinical experience.

It was also a little surprising to learn that despite their high fees, most of these clinics are not making a profit. For clients, the annual costs of attending a longevity clinic range between $10,000 and $150,000, according to Fountain Life, a company with clinics in Florida and Prague. But only 39% of the surveyed clinics said they were turning a profit and 30% said they were “approaching breaking even,” while 16% said they were operating at a loss.

Proponents of longevity clinics have high hopes for the field. They see longevity medicine as nothing short of a revolution—a move away from reactive treatments and toward proactive health maintenance. But these survey results show just how far they have to go.

This article first appeared in The Checkup, MIT Technology Review’s weekly biotech newsletter. To receive it in your inbox every Thursday, and read articles like this first, sign up here.

Love or immortality: A short story

1.

Sophie and Martin are at the 2012 Gordon Research Conference on the Biology of Aging in Ventura, California. It is a foggy February weekend. Both are disappointed about how little sun there is on the California beach.

They are two graduate students—Sophie in her sixth and final year, Martin in his fourth—who have traveled from different East Coast cities to present posters on their work. Martin’s shows health data collected from supercentenarians compared with the general Medicare population, capturing the diseases that are less and more common in the populations. Sophie is presenting on her recently accepted first-author paper in Aging Cell on two specific genes that, when activated, extend lifespan in C. elegans roundworms, the model organism of her research. 

2.

Sophie walks by Martin’s poster after she is done presenting her own. She is not immediately impressed by his work. It is not published, for one thing. But she sees how it is attention-grabbing and relevant, even necessary. He has a little crowd listening to him. He notices her—a frowning girl—standing in the back and begins to talk louder, hoping she hears.

“Supercentenarians are much less likely to have seven diseases,” he says, pointing to his poster. “Alzheimer’s, heart failure, diabetes, depression, prostate cancer, hip fracture, and chronic kidney disease. Though they have higher instances of four diseases, which are arthritis, cataracts, osteoporosis, and glaucoma. These aren’t linked to mortality, but they do affect quality of life.”

What stands out to Sophie is the confidence in Martin’s voice, despite the unsurprising nature of the findings. She admires that sound, its sturdiness. She makes note of his name and plans to seek him out. 

3.

They find one another in the hotel bar among other graduate students. The students are talking about the logistics of their futures: Who is going for a postdoc, who will opt for industry, do any have job offers already, where will their research have the most impact, is it worth spending years working toward something so uncertain? They stay up too late, dissecting journal articles they’ve read as if they were debating politics. They enjoy the freedom away from their labs and PIs. 

Martin says, again with that confidence, that he will become a professor. Sophie says she likely won’t go down that path. She has received an offer to start as a scientist at an aging research startup called Abyssinian Bio, after she defends. Martin says, “Wouldn’t your work make more sense in an academic setting, where you have more freedom and power over what you do?” She says, “But that could be years from now and I want to start my real life, so …” 

4-18.

Martin is enamored with Sophie. She is not only brilliant; she is helpful. She strengthens his papers with precise edits and grounds his arguments with stronger evidence. Sophie is enamored with Martin. He is not only ambitious; he is supportive and adventurous. He encourages her to try new activities and tools, both in and out of work, like learning to ride a motorcycle or using CRISPR.

Martin visits Sophie in San Francisco whenever he can, which amounts to a weekend or two every other month. After two years, their long-distance relationship is taking its toll. They want more weekends, more months, more everything together. They make plans for him to get a postdoc near her, but after multiple rejections from the labs where he most wants to work, his resentment toward academia grows. 

“They don’t see the value of my work,” he says.

19.

“Join Abyssinian,” Sophie offers.

The company is growing. They want more researchers with data science backgrounds. He takes the job, drawn more by their future together than by the science.

20-35.

For a long time, they are happy. They marry. They do their research. They travel. Sophie visits Martin’s extended family in France. Martin goes with Sophie to her cousin’s wedding in Taipei. They get a dog. The dog dies. They are both devastated but increasingly motivated to better understand the mechanisms of aging. Maybe their next dog will have the opportunity to live longer. They do not get a next dog.

Sophie moves up at Abyssinian. Despite being in industry, her work is published in well-respected journals. She collaborates well with her colleagues. Eventually, she is promoted to executive director of research. 

Martin stalls at the rank of principal scientist, and though Sophie is technically his boss—or his boss’s boss—he genuinely doesn’t mind when others call him “Dr. Sophie Xie’s husband.”

40.

At dinner on his 35th birthday, a friend jokes that Martin is now middle-aged. Sophie laughs and agrees, though she is older than Martin. Martin joins in the laughter, but this small comment unlocks a sense of urgency inside him. What once felt hypothetical—his own death, the death of his wife—now appears very close. He can feel his wrinkles forming.  

First come the subtle shifts in how he talks about his research and Abyssinian’s work. He wants to “defeat” and “obliterate” aging, which he comes to describe as humankind’s “greatest adversary.” 

43.

He begins taking supplements touted by tech influencers. He goes on a calorie-restricted diet. He gets weekly vitamin IV sessions. He looks into blood transfusions from young donors, but Sophie tells him to stop with all the fake science. She says he’s being ridiculous, that what he’s doing could be dangerous.  

Martin, for the first time, sees Sophie differently. Not without love, but love burdened by an opposing weight, what others might recognize as resentment. Sophie is dedicated to the demands of her growing department. Martin thinks she is not taking the task of living longer seriously enough. He does not want her to die. He does not want to die. 

Nobody at Abyssinian is taking the task of living longer seriously enough. Of all the aging bio startups he could have ended up at, how has he ended up at one with such modest—no, lazy—goals? He begins publicly dismissing basic research as “too slow” and “too limited,” which offends many of his and Sophie’s colleagues. 

Sophie defends him, says he is still doing good work, despite the evidence. She is busy, traveling often for conferences, and mistakenly misclassifies the changes in Martin’s attitude as temporary outliers.

44.

One day, during a meeting, Martin says to Jerry, a well-­respected scientist at Abyssinian and in the electron microscopy imaging community at large, that EM is an outdated, old, crusty technology. Martin says it is stupid to use it when there are more advanced, cutting-edge methods, like cryo-EM and super-resolution microscopy. Martin has always been outspoken, but this instance veers into rudeness. 

At home, Martin and Sophie argue. Initially, they argue about whether tools of the past can be useful to their work. Then the argument morphs. What is the true purpose of their research? Martin says it’s called anti-aging research for a reason: It’s to defy aging! Sophie says she’s never called her work anti-aging research; she calls it aging research or research into the biology of aging. And Abyssinian’s overarching mission is more simply to find druggable targets for chronic and age-related diseases. Occasionally, the company’s marketing arm will push out messaging about extending the human lifespan by 20 years, but that has nothing to do with scientists like them in R&D. Martin seethes. Only 20 years! What about hundreds? Thousands? 

45-49.

They continue to argue and the arguments are roundabout, typically ending with Sophie crying, absconding to her sister’s house, and the two of them not speaking for short periods of time.

50.

What hurts Sophie most is Martin’s persistent dismissal of death as merely an engineering problem to be solved. Sophie thinks of the ways the C. elegans she observes regulate their lifespans in response to environmental stress. The complex dance of genes and proteins that orchestrates their aging process. In the previous month’s experiment, a seemingly simple mutation produced unexpected effects across three generations of worms. Nature’s complexity still humbles her daily. There is still so much unknown. 

Martin is at the kitchen counter, methodically crushing his evening supplements into powder. “I’m trying to save humanity. And all you want to do is sit in the lab to watch worms die.”

50.

Martin blames the past. He realizes he should have tried harder to become a professor. Let Sophie make the industry money—he could have had academic clout. Professor Warwick. It would have had a nice sound to it. To his dismay, everyone in his lab calls him Martin. Abyssinian has a first-name policy. Something about flat hierarchies making for better collaboration. Good ideas could come from anyone, even a lowly, unintelligent senior associate scientist in Martin’s lab who barely understands how to process a data set. A great idea could come from anyone at all—except him, apparently. Sophie has made that clear.

51-59.

They live in a tenuous peace for some time, perfecting the art of careful scheduling: separate coffee times, meetings avoided, short conversations that stick to the day-to-day facts of their lives.

60.

Then Martin stands up to interrupt a presentation by the VP of research to announce that studying natural aging is pointless since they will soon eliminate it entirely. While Jerry may have shrugged off Martin’s aggressiveness, the VP does not. This leads to a blowout fight between Martin and many of his colleagues, in which Martin refuses to apologize and calls them all shortsighted idiots. 

Sophie watches with a mixture of fear and awe. Martin thinks: Can’t she, my wife, just side with me this once? 

61.

Back at home:

Martin at the kitchen counter, methodically crushing his evening supplements into powder. “I’m trying to save humanity.” He taps the powder into his protein shake with the precision of a scientist measuring reagents. “And all you want to do is sit in the lab to watch worms die.”

Sophie observes his familiar movements, now foreign in their desperation. The kitchen light catches the silver spreading at his temples and on his chin—the very evidence of aging he is trying so hard to erase.

“That’s not true,” she says.

Martin gulps down his shake.

“What about us? What about children?”

Martin coughs, then laughs, a sound that makes Sophie flinch. “Why would we have children now? You certainly don’t have the time. But if we solve aging, which I believe we can, we’d have all the time in the world.”

“We used to talk about starting a family.”

“Any children we have should be born into a world where we already know they never have to die.”

“We could both make the time. I want to grow old together—”

All Martin hears are promises that lead to nothing, nowhere.  

“You want us to deteriorate? To watch each other decay?”

“I want a real life.”

“So you’re choosing death. You’re choosing limitation. Mediocrity.”

64.

Martin doesn’t hear from his wife for four days, despite texting her 16 times—12 too many, by his count. He finally breaks down enough to call her in the evening, after a couple of glasses of aged whisky (a gift from a former colleague, which Martin has rarely touched and kept hidden in the far back of a desk drawer). 

Voicemail. And after this morning’s text, still no glimmering ellipsis bubble to indicate Sophie’s typing. 

66.

Forget her, he thinks, leaning back in his Steelcase chair, adjusted specifically for his long runner’s legs and shorter­-than-average torso. At 39, Martin’s spreadsheets of vitals now show an upward trajectory; proof of his ability to reverse his biological age. Sophie does not appreciate this. He stares out his office window, down at the employees crawling around Abyssinian Bio’s main quad. How small, he thinks. How significantly unaware of the future’s true possibilities. Sophie is like them. 

67.

Forget her, he thinks again as he turns down a bay toward Robert, one of his struggling postdocs, who is sitting at his bench staring at his laptop. As Martin approaches, Robert minimizes several windows, leaving only his home screen behind.

“Where are you at with the NAD+ data?” Martin asks.

Robert shifts in his chair to face Martin. The skin of his neck grows red and splotchy. Martin stares at it in disgust.

“Well?” he asks again. 

“Oh, I was told not to work on that anymore?” The boy has a tendency to speak in the lilt of questions. 

“By who?” Martin demands.

“Uh, Sophie?” 

“I see. Well, I expect new data by end of day.” 

“Oh, but—”

Martin narrows his eyes. The red splotches on Robert’s neck grow larger. 

“Um, okay,” the boy says, returning his focus to the computer. 

Martin decides a response is called for …

70.

Immortality Promise

I am immortal. This doesn’t make me special. In fact, most people on Earth are immortal. I am 6,000 years old. Now, 6,000 years of existence give one a certain perspective. I remember back when genetic engineering and knowledge about the processes behind aging were still in their infancy. Oh, how people argued and protested.

“It’s unethical!”

“We’ll kill the Earth if there’s no death!”

“Immortal people won’t be motivated to do anything! We’ll become a useless civilization living under our AI overlords!” 

I believed back then, and now I know. Their concerns had no ground to stand on.

Eternal life isn’t even remarkable anymore, but being among its architects and early believers still garners respect from the world. The elegance of my team’s solution continues to fill me with pride. We didn’t just halt aging; we mastered it. My cellular machinery hums with an efficiency that would make evolution herself jealous.

Those early protesters—bless their mortal, no-longer-­beating hearts—never grasped the biological imperative of what we were doing. Nature had already created functionally immortal organisms—the hydra, certain jellyfish species, even some plants. We simply perfected what evolution had sketched out. The supposed ethical concerns melted away once people understood that we weren’t defying nature. We were fulfilling its potential.

Today, those who did not want to be immortal aren’t around. Simple as that. Those who are here do care about the planet more than ever! There are almost no diseases, and we’re all very productive people. Young adults—or should I say young-looking adults—are naturally restless and energetic. And with all this life, you have the added benefit of not wasting your time on a career you might hate! You get to try different things and find out what you’re really good at and where you’re appreciated! Life is not short! Resources are plentiful!

Of course, biological immortality doesn’t equal invincibility. People still die. Just not very often. My colleagues in materials science developed our modern protective exoskeletons. They’re elegant solutions, though I prefer to rely on my enhanced reflexes and reinforced skeletal structure most days. 

The population concerns proved mathematically unfounded. Stable reproduction rates emerged naturally once people realized they had unlimited time to start families. I’ve had four sets of children across 6,000 years, each born when I felt truly ready to pass on another iteration of my accumulated knowledge. With more life, people have much more patience. 

Now we are on to bigger and more ambitious projects. We conquered survival of individuals. The next step: survival of our species in this universe. The sun’s eventual death poses an interesting challenge, but nothing we can’t handle. We have colonized five planets and two moons in our solar system, and we will colonize more. Humanity will adapt to whatever environment we encounter. That’s what we do.

My ancient motorcycle remains my favorite indulgence. I love taking it for long cruises on the old Earth roads that remain intact. The neural interface is state-of-the-art, of course. But mostly I keep it because it reminds me of earlier times, when we thought death was inevitable and life was limited to a single planet. The future stretches out before us like an infinity I helped create—yet another masterpiece in the eternal gallery of human evolution.

71.

Martin feels better after writing it out. He rereads it a couple times, feels even better. Then he has the idea to send his writing to the department administrator. He asks her to create a new tab on his lab page, titled “Immortality Promise,” and to post his piece there. That will get his message across to Sophie and everyone at Abyssinian. 

72.

Sophie’s boss, Ray, is the first to email her. The subject line: “martn” [sic]. No further words in the body. Ray is known to be short and blunt in all his communications, but his meaning is always clear. They’ve had enough conversations about Martin by then. She is already in the process of slowly shutting down his projects, has been ignoring his texts and calls because of this. Now she has to move even faster. 

73.

Sophie leaves her office and goes into the lab. As an executive, she is not expected to do experiments, but watching a thousand tiny worms crawl across their agar plates soothes her. Each of the ones she now looks at carries a fluorescent marker she designed to track mitochondrial dynamics during aging. The green glow pulses with their movements, like stars blinking in a microscopic galaxy. She spent years developing this strain of C. elegans, carefully selecting for longevity without sacrificing health. The worms that lived longest weren’t always the healthiest—a truth about aging that seemed to elude Martin. Those worms taught her more about the genuine complexity of aging. Just last week, she observed something unexpected: The mitochondrial networks in her long-lived strains showed subtle patterns of reorganization never documented before. The discovery felt intimate, like being trusted with a secret.

“How are things looking?” Jerry appears beside her. “That new strain expressing the dual markers?”

Sophie nods, adjusting the focus. “Look at this network pattern. It’s different from anything in the literature.” She shifts aside so Jerry can see. This is what she loves about science: the genuine puzzles, the patient observation, the slow accumulation of knowledge that, while far removed from a specific application, could someday help people age with dignity.

“Beautiful,” Jerry murmurs. He straightens. “I heard about Martin’s … post.”

Sophie closes her eyes for a moment, the image of the mitochondrial networks still floating in her vision. She’s read Martin’s “Immortality Promise” piece three times, each more painful than the last. Not because of its grandiose claims—those were comically disconnected from reality—but because of what it’s revealed about her husband. The writing pulsed with a frightening certainty, a complete absence of doubt or wonder. Gone was the scientist who once spent many lively evenings debating with her about the evolutionary purpose of aging, who delighted in being proved wrong because it meant learning something new. 

74.

She sees in his words a man who has abandoned the fundamental principles of science. His piece reads like a religious text or science fiction story, casting himself as the hero. He isn’t pursuing research anymore. He hasn’t been for a long time. 

She wonders how and when he arrived there. The change in Martin didn’t take place overnight. It was gradual, almost imperceptible—not unlike watching someone age. It wasn’t easy to notice if you saw the person every day; Sophie feels guilty for not noticing. Then again, she read a new study out a few months ago from Stanford researchers that found people do not age linearly but in spurts—specifically, around 44 and 60. Shifts in the body lead to sudden accelerations of change. If she’s honest with herself, she knew this was happening to Martin, to their relationship. But she chose to ignore it, give other problems precedence. Now it is too late. Maybe if she’d addressed the conditions right before the spike—but how? wasn’t it inevitable?—he would not have gone from scientist to fanatic.

75.

“You’re giving the keynote at next month’s Gordon conference,” Jerry reminds her, pulling her back to reality. “Don’t let this overshadow that.”

She manages a small smile. Her work has always been methodical, built on careful observation and respect for the fundamental mysteries of biology. The keynote speech represents more than five years of research: countless hours of guiding her teams, of exciting discussions among her peers, of watching worms age and die, of documenting every detail of their cellular changes. It is one of the biggest honors of her career. There is poetry in it, she thinks—in the collisions between discoveries and failures. 

76.

The knock on her office door comes at 2:45. Linda from HR, right on schedule. Sophie walks with her to conference room B2, two floors below, where Martin’s group resides. Through the glass walls of each lab, they see scientists working at their benches. One adjusts a microscope’s focus. Another pipettes clear liquid into rows of tubes. Three researchers point at data on a screen. Each person is investigating some aspect of aging, one careful experiment at a time. The work will continue, with or without Martin.

In the conference room, Sophie opens her laptop and pulls up the folder of evidence. She has been collecting it for months. Martin’s emails to colleagues, complaints from collaborators and direct reports, and finally, his “Immortality Promise” piece. The documentation is thorough, organized chronologically. She has labeled each file with dates and brief descriptions, as she would for any other data.

77.

Martin walks in at 3:00. Linda from HR shifts in her chair. Sophie is the one to hand the papers over to Martin; this much she owes him. They contain words like “termination” and “effective immediately.” Martin’s face complicates itself when he looks them over. Sophie hands over a pen and he signs quickly.  

He stands, adjusts his shirt cuffs, and walks to the door. He turns back.

“I’ll prove you wrong,” he says, looking at Sophie. But what stands out to her is the crack in his voice on the last word. 

Sophie watches him leave. She picks up the signed papers and hands them to Linda, and then walks out herself. 

Alexandra Chang is the author of Days of Distraction and Tomb Sweeping and is a National Book Foundation 5 under 35 honoree. She lives in Camarillo, California.

A new biosensor can detect bird flu in five minutes

Over the winter, eggs suddenly became all but impossible to buy. As a bird flu outbreak rippled through dairy and poultry farms, grocery stores struggled to keep them on shelves. The shortages and record-high prices in February raised costs dramatically for restaurants and bakeries and led some shoppers to skip the breakfast staple entirely. But a team based at Washington University in St. Louis has developed a device that could help slow future outbreaks by detecting bird flu in air samples in just five minutes. 

Bird flu is an airborne virus that spreads between birds and other animals. Outbreaks on poultry and dairy farms are devastating; mass culling of exposed animals can be the only way to stem outbreaks. Some bird flu strains have also infected humans, though this is rare. As of early March, there had been 70 human cases and one confirmed death in the US, according to the Centers for Disease Control and Prevention.

The most common way to detect bird flu involves swabbing potentially contaminated sites and sequencing the DNA that’s been collected, a process that can take up to 48 hours.

The new device samples the air in real time, running the samples past a specialized biosensor every five minutes. The sensor has strands of genetic material called aptamers that were used to bind specifically to the virus. When that happens, it creates a detectable electrical change. The research, published in ACS Sensors in February, may help farmers contain future outbreaks.

Part of the group’s work was devising a way to deliver airborne virus particles to the sensor. 

With bird flu, says Rajan Chakrabarty, a professor of energy, environmental, and chemical engineering at Washington University and lead author of the paper, “the bad apple is surrounded by a million or a billion good apples.” He adds, “The challenge was to take an airborne pathogen and get it into a liquid form to sample.”

The team accomplished this by designing a microwave-­size box that sucks in large volumes of air and spins it in a cyclone-like motion so that particles stick to liquid-coated walls. The process seamlessly produces a liquid drip that is pumped to the highly sensitive biosensor. 

Though the system is promising, its effectiveness in real-world conditions remains uncertain, says Sungjun Park, an associate professor of electrical and computer engineering at Ajou University in South Korea, who was not involved in the study. Dirt and other particles in farm air could hinder its performance. “The study does not extensively discuss the device’s performance in complex real-world air samples,” Park says. 

But Chakrabarty is optimistic that it will be commercially viable after further testing and is already working with a biotech company to scale it up. He hopes to develop a biosensor chip that detects multiple pathogens at once. 

Carly Kay is a science writer based in Santa Cruz, California.

Game of clones: Colossal’s new wolves are cute, but are they dire?

Somewhere in the northern US, drones fly over a 2,000-acre preserve, protected by a nine-foot fence built to zoo standards. It is off-limits to curious visitors, especially those with a passion for epic fantasies or mythical creatures.

The reason for such tight security? Inside the preserve roam three striking snow-white wolves—which a startup called Colossal Biosciences says are members of a species that went extinct 13,000 years ago, now reborn via biotechnology.

For several years now, the Texas-based company has been in the news for its plans to re-create woolly mammoths someday. But now it’s making a bold new claim—that it has actually “de-extincted” an animal called the dire wolf.

And that could be another reason for the high fences and secret location—to fend off scientific critics, some of whom have already been howling that the company is a “scam” perpetrating “elephantine fantasies” on the public and engaging in “pure hype.”

Dire wolves were large, big-jawed members of the canine family. More than 400 of their skulls have been recovered from the La Brea Tar Pits in California. Ultimately they were replaced by smaller relatives like the gray wolf.

In its effort to re-create the animal, Colossal says, it extracted DNA information from dire wolf bones and used gene editing to introduce some of those elements into cells from gray wolves. It then used a cloning procedure to turn the cells into three actual animals. 

The animals include two males, Romulus and Remus, born in October, and one female, Khaleesi, whose name is a reference to the TV series Game of Thrones, in which fictional dire wolves play a part.

Two dire wolves are seen at 3 months old.
Two of the “dire wolves” at three months old.
COLOSSAL BIOSCIENCES

Each animal, the company says, has 20 genetic changes across 14 genes designed to make them larger, change their facial features, and give them a snow-white appearance.

Some scientists reject the company’s claim that the new animals are a revival of the extinct creatures, since in reality dire wolves and gray wolves are different species separated by a few million of years of evolution and several million letters of DNA.

“I would say such an animal is not a dire wolf and it’s not correct to say dire wolves have been brought back from extinction. It’s a modified gray wolf,” says Anders Bergström, a professor at the University of East Anglia who specializes in the evolution of canines. “Twenty changes is not nearly enough. But it could get you a strange-looking gray wolf.”

Beth Shapiro, an expert on ancient DNA who is now on a three-year sabbatical from the University of California, Santa Cruz, as the company’s CSO, acknowledged in an interview that other scientists would bristle at the claim.

“What we’re going to have here is a philosophical argument about whether we should call it a dire wolf or call it something else,” Shapiro said. Asked point blank to call the animal a dire wolf, she hesitated but then did so.

“It is a dire wolf,” she said. “I feel like I say that, and then all of my taxonomist friends will be like, ‘Okay, I’m done with her.’ But it’s not a gray wolf. It doesn’t look like a gray wolf.”

Dire or not, the new wolves demonstrate that science is becoming more deft in its control over the genomes of animals—and point to how that skill could help in conservation. As part of the project, Colossal says, it also cloned several red wolves, an American species that’s the most endangered wolf in the world.

But that isn’t as dramatic as the supposed rebirth of an extinct animal with a large cultural following. “The motivation really is to develop tools that we can use to stop species from becoming extinct. Do we need ancient DNA for that? Maybe not,” says Shapiro. “Does it bring more attention to it so that maybe people get excited about the idea that we can use biotechnology for conservation? Probably.”

Secret project

Colossal was founded in 2021 after founder Ben Lamm, a software entrepreneur, visited the Harvard geneticist George Church and learned about a far-out and still mostly theoretical project to re-create woolly mammoths. The idea is to release herds of them in cold regions, like Siberia, and restore an ecological balance that keeps greenhouse gases trapped in the permafrost.

Lamm has unexpectedly been able to raise more than $400 million from investors to back the plan, and Forbes reported that he is now a multibillionaire, at least on paper, thanks to the $10 billion value assigned to the startup.

Ben, Beth, and George of Colossal Biosciences pose with dire wolf pups.
From left to right: Beth Shapiro, George Church, and Ben Lamm pose with the pups.
COLOSSAL BIOSCIENCES

As Lamm showed he could raise money for Colossal’s ideas, it soon expanded beyond its effort to modify elephants. It publicly announced a bid to re-create the thylacine, a marsupial predator hunted to extinction, and then, in 2023, it started planning to resurrect the dodo bird—the effort that brought Shapiro to the company.

So far, none of those signature projects have actually resulted in a live animal with ancient genes. 

Each faces dire practical issues. With elephants, it was that their pregnancies last two years, longer than those in any other species. Testing out mammoth designs would be impossibly slow. With the dodo bird, it was that no one has ever figured out how to genetically modify pigeons, the family of birds to which the dodo belonged and from which a new dodo would have to be crafted. One of Lamm’s other favorite targets—the Steller’s sea cow, which disappeared around 1770—has no obvious surrogate of any kind.   

But creating a wolf was feasible. Over 1,500 dogs had been cloned, primarily by one company in South Korea. Researchers in Asia had even used dog eggs and dog mothers to produce both coyote and wolf clones. That’s not surprising, since all these species are closely enough related to interbreed.

“Just thinking about surrogacy for the dire wolf … it was like ‘Oh, yeah,’” recalls Shapiro. “Surrogacy there would be really straightforward.”

Dire wolves did present some new problems. One was the lack of any clear ecological purpose in reviving animals that disappeared during the Pleistocene epoch and are usually portrayed as ferocious predators with slavering jaws. “People have weird feelings about things that, you know, may or may not eat people or livestock,” Shapiro says.

The technical challenge was there was still no accurate DNA sequence of a dire wolf. A 2021 effort to obtain DNA from old bones had yielded only a tiny amount, not enough to accurately decode the genome in detail. And without a detailed gene map, Colossal wouldn’t be able see what genetic differences they would need to install in gray wolves, the species they intended to alter.

Shapiro says she went back to museums, including the Idaho Museum of Natural History, and eventually got permission to cut off more bone from a 72,0000-year-old skull that’s on display there. She also got a tooth from a 13,000-year-old skull held in another museum. which she drilled into herself.

This time the bones yielded far more DNA and a much more complete gene map. A paper describing the detailed sequence is being submitted for publication; its authors include George R.R. Martin, the fantasy author whose books were turned into the HBO series Game of Thrones, and in which dire wolves appear as the characters’ magical companions.

In addition to placing dire wolves more firmly in the Canidae family tree (they’re slightly closer to jackals than to gray wolves, but more than 99.9% identical to both at a genetic level) and determining when dire wolves split from the pack (about 4 to 5 million years ago), the team also located around 80 genes where dire wolves seemed to be most different. If you wanted to turn a gray wolf into a dire wolf, this would be the obvious list to start from.

Crying wolf

Colossal then began the process of using base editing, an updated form of the CRISPR gene-modification technique, to introduce some of those exact DNA variations into blood cells of a gray wolf kept in its labs. Each additional edit, the company  hoped, would make the eventual animal a little more dire-wolf-like, even it involved changing just a single letter of a gene.

Shapiro says all the edits using information from the ancient dire wolf were made to “genetic enhancers,” bits of DNA that help control how strongly certain genes are expressed. These can influence how big animals grow, as well as affecting the shape of their ears, faces, and skulls. This tactic was not as dramatic as intervening right in the middle of a gene, which would change what protein is made. But it was less risky—more like turning knobs on an unfamiliar radio than cutting wires and replacing circuits.

That left the scientists to engineer into the animals what would become their showstopper trait—the dramatic white fur. Shapiro says the genome code indicated that dire wolves might have had light coats. But the specific pigment genes involved are linked to a risk of albinism, deafness, and blindness, and they didn’t want sick wolves.

That’s when Colossal opted for a shortcut. Instead of reproducing precise DNA variants seen in dire wolves, they disabled two genes entirely. In dogs and other species, the absence of those genes is known to produce light fur.

The decision to make the wolves white did result in dramatic photos of the animals. “It’s the most striking thing about them,” says Mairin Balisi, a paleontologist who studies dire wolf fossils. But she doubts it reflects what the animals actually looked like: “A white coat might make sense if you are in a snowy landscape, but one of the places where dire wolves were most abundant was around Los Angeles and the tar pits, and it was not a snowy landscape even in the Ice Age. If you look at mammals in this region today, they are not white. I am just confused by the declaration that dire wolves are back.”

Bergström also says he doesn’t think the edits add up to a dire wolf. “I doubt that 20 changes are enough to turn a gray wolf to a dire wolf. You’d probably need hundreds or thousands of changes—no one really knows,” he says. “This is one of those unsolved questions in biology. People argue [about] the extent to which many small differences make a species distinct, versus a small number of big-effect differences. Nobody knows, but I lean to the ‘many small differences’ view.”

Some genes have big, visible effects—changing a single gene can make a dog hairless, for instance. But it might be many more small changes that account for the difference in size and appearance between, say, a Great Dane and a Chihuahua. And that is just looks. Bergström says science has much less idea which changes would account for behavior—even if we could tell from a genome how an extinct animal acted, which we can’t.

“A lot of people are quite skeptical of what they are doing,” Bergström says of Colossal. “But I still think it’s interesting that someone is trying. It takes a lot of money and resources, and if we did have the technology to bring species back from extinction, I do think that would be useful. We drive species to extinction, sometimes very rapidly, and that is a shame.”

Cloning with dogs

By last August, the gray wolf cells had been edited, and it was time to try cloning those cells and producing animals. Shapiro says her company transferred 40 to 50 cloned embryos apiece into six surrogate dogs. That led to three pregnancies, from which four dogs were born. One of the four, Khaleesi’s sister, died 10 days after birth from an intestinal infection, deemed unrelated to the cloning process. “That was the only puppy that didn’t make it,” says Shapiro. Two other fetal clones were reabsorbed during pregnancy, which means they disintegrated, a fairly common occurrence in dogs.

These days the white wolves are able to freely roam around a large area. They don’t have radio collars, but they are watched by cameras and are trained to come to their caretakers to get fed, which offers a chance to weigh them as they cross a scale in the ground. The 10 staff members attending to them can see them up close, though they’re now too big to handle the way the caretakers could when they were puppies.

The pups are being monitored through the different stages of their development but will not be put on public display.
COLOSSAL BIOSCIENCES

Whatever species these animals are, it’s not obvious what their future will be. They don’t seem to have a conservation purpose, and Lamm says he isn’t trying to profit from them.

“We’re not making money off the dire wolves. That’s not our business plan,” Lamm said in an interview with MIT Technology Review. He added that the animals would also not be put on display for the public, since “we’re not in the business of attractions.”

At least not in-person attractions. But every aspect of the project has been filmed, and in February, the company inked a deal to produce a docuseries about its exploits. That same month it also hired as its marketing chief a Hollywood executive who previously worked on big-budget “monster movies.”

And there are signs that de-extinction, in Colossal’s hands, has the potential to generate nearly out-of-control of attention, much like that scene in the original King Kong when the giant ape—captured by a filmmaker—breaks its chains under the flashes of the cameras.

For instance company’s first creation, mice with shaggy, mammoth-like hair, was announced only five weeks ago, yet there are already unauthorized sales of throw pillows and T-shirts (they read “Legalize Woolly Mice”), as well as some “serious security issues” involving unannounced visitors, Lamm says.

“We’ve had people show up to our labs because they want the woolly mouse,” Lamm says. “We’re worried about that from a security perspective [for] the wolves, because you’re going to have all the Game of Thrones people. You’re going to have a lot of people that want to see these animals.”  

Lamm said that in light of his concerns about unruly fans, diagrams of the ecological preserve provided to the media had been altered so that no internet “sleuths” could use them to guess its location.

Brain-computer interfaces face a critical test

Tech companies are always trying out new ways for people to interact with computers—consider efforts like Google Glass, the Apple Watch, and Amazon’s Alexa. You’ve probably used at least one.

But the most radical option has been tried by fewer than 100 people on Earth—those who have lived for months or years with implanted brain-computer interfaces, or BCIs.

Implanted BCIs are electrodes put in paralyzed people’s brains so they can use imagined movements to send commands from their neurons through a wire, or via radio, to a computer. In this way, they can control a computer cursor or, in few cases, produce speech.  

Recently, this field has taken some strides toward real practical applications. About 25 clinical trials of BCI implants are currently underway. And this year MIT Technology Review readers have selected these brain-computer interfaces as their addition to our annual list of 10 Breakthrough Technologies, published in January.

BCIs won by a landslide to become the “11th Breakthrough,” as we call it. It beat out three runners-up: continuous glucose monitors, hyperrealistic deepfakes, and methane-detecting satellites.

The impression of progress comes thanks to a small group of companies that are actively recruiting volunteers to try BCIs in clinical trials. They are Neuralink, backed by the world’s richest person, Elon Musk; New York–based Synchron; and China’s Neuracle Neuroscience. 

Each is trialing interfaces with the eventual goal of getting the field’s first implanted BCI approved for sale. 

“I call it the translation era,” says Michelle Patrick-Krueger, a research scientist who carried out a detailed survey of BCI trials with neuroengineer Jose Luis Contreras-Vidal at the University of Houston. “In the past couple of years there has been considerable private investment. That creates excitement and allows companies to accelerate.”

That’s a big change, since for years BCIs have been more like a neuroscience parlor trick, generating lots of headlines but little actual help to patients. 

Patrick-Krueger says the first time a person controlled a computer cursor from a brain implant was in 1998. That was followed by a slow drip-drip of tests in which university researchers would find a single volunteer, install an implant, and carry out studies for months or years.

Over 26 years, Patrick-Krueger says, she was able to document a grand total of 71 patients who’ve ever controlled a computer directly with their neurons. 

That means you are more likely to be friends with a Mega Millions jackpot winner than know someone with a BCI.

These studies did prove that people could use their neurons to play Pong, move a robot arm, and even speak through a computer. But such demonstrations are of no practical help to people with paralysis severe enough to benefit from a brain-controlled computer, because these implants are not yet widely available. 

“One thing is to have them work, and another is how to actually deploy them,” says Contreras-Vidal. “Also, behind any great news are probably technical issues that need to be addressed.” These include questions about how long an implant will last and how much control it offers patients.

Larger trials from three companies are now trying to resolve these questions and set the groundwork for a real product.

One company, Synchron, uses a stent with electrodes on it that’s inserted into a brain vessel via a vein in the neck. Synchron has implanted its “stentrode” in 10 volunteers, six in the US and four in Australia—the most simultaneous volunteers reported by any BCI group. 

The stentrode collects limited brain signals, so it gives users only a basic on/off type of control signal, or what Synchron calls a “switch.” That isn’t going to let a paralyzed person use Photoshop. But it’s enough to toggle through software menus or select among prewritten messages.

Tom Oxley, Synchron’s CEO, says the advantage of the stentrode is that it is “as simple as possible.” That, he believes, will make his brain-computer interface “scalable” to more people, especially since installing it doesn’t involve brain surgery. 

Synchron might be ahead, but it’s still in an exploratory phase. A “pivotal” study, the kind used to persuade regulators to allow sales of a specific version of the device, has yet to be scheduled. So there’s no timeline for a product.  

Neuralink, meanwhile, has disclosed that three volunteers have received its implant, the N1, which consists of multiple fine electrode threads inserted directly into the brain through a hole drilled in the skull. 

More electrodes mean more neural activity is captured. Neuralink’s first volunteer, Noland Arbaugh, has shown off how he can guide a cursor around a screen in two dimensions and click, letting him play video games like Civilization or online chess.

Finally, Neuracle says it is running two trials in China and one in the US. Its implant consists of a patch of electrodes placed on top of the brain. In a report, the company said a paralyzed volunteer is using the system to stimulate electrodes in his arm, causing his hand to close in a grasp. 

But details remain sparse. A Neuracle executive would only say that “several” people had received its implant.

Because Neuracle’s patient count isn’t public, it wasn’t included in Patrick-Krueger’s tally. In fact, there’s no information at all in the medical literature on about a quarter of brain-implant volunteers so far, so she counted them using press releases or by e-mailing research teams.

Her BCI survey yielded other insights. According to her data, implants have lasted as long as 15 years, more than half of patients are in the US, and roughly 75% of BCI recipients have been male. 

The data can’t answer the big question, though. And that is whether implanted BCIs will progress from breakthrough demonstrations into breakout products, the kind that help many people.

“In the next five to 10 years, it’s either going to translate into a product or it’ll still stay in research,” Patrick-Krueger says. “I do feel very confident there will be a breakout.”

“Spare” living human bodies might provide us with organs for transplantation

This week, MIT Technology Review published a piece on bodyoids—living bodies that cannot think or feel pain. In the piece, a trio of scientists argue that advances in biotechnology will soon allow us to create “spare” human bodies that could be used for research, or to provide organs for donation.

If you find your skin crawling at this point, you’re not the only one. It’s a creepy idea, straight from the more horrible corners of science fiction. But bodyoids could be used for good. And if they are truly unaware and unable to think, the use of bodyoids wouldn’t cross “most people’s ethical lines,” the authors argue. I’m not so sure.

Either way, there’s no doubt that developments in science and biotechnology are bringing us closer to the potential reality of bodyoids. And the idea is already stirring plenty of ethical debate and controversy.

One of the main arguments made for bodyoids is that they could provide spare human organs. There’s a huge shortage of organs for transplantation. More than 100,000 people in the US are waiting for a transplant, and 17 people on that waiting list die every day. Human bodyoids could serve as a new source.

Scientists are working on other potential solutions to this problem. One approach is the use of gene-edited animal organs. Animal organs don’t typically last inside human bodies—our immune systems will reject them as “foreign.” But a few companies are creating pigs with a series of gene edits that make their organs more acceptable to human bodies.

A handful of living people have received gene-edited pig organs. David Bennett Sr. was the first person to get a gene-edited pig heart, in 2022, and Richard Slayman was the first to get a kidney, in early 2024. Unfortunately, both men died around two months after their surgery.

But Towana Looney, the third living person to receive a gene-edited pig kidney, has been doing well. She had her transplant surgery in late November of last year. “I am full of energy. I got an appetite I’ve never had in eight years,” she said at the time. “I can put my hand on this kidney and feel it buzzing.” She returned home in February.

At least one company is taking more of a bodyoid-like approach. Renewal Bio, a biotech company based in Israel, hopes to grow “embryo-stage versions of people” for replacement organs.

Their approach is based on advances in the development of “synthetic embryos.” (I’m putting that term in quotation marks because, while it’s the simplest descriptor of what they are, a lot of scientists hate the term.)

Embryos start with the union of an egg cell and a sperm cell. But scientists have been working on ways to make embryos using stem cells instead. Under the right conditions, these cells can divide into structures that look a lot like a typical embryo.

Scientists don’t know how far these embryo-like structures will be able to develop. But they’re already using them to try to get cows and monkeys pregnant.

And no one really knows how to think about synthetic human embryos. Scientists don’t even really know what to call them. Rules stipulate that typical human embryos may be grown in the lab for a maximum of 14 days. Should the same rules apply to synthetic ones?

The very existence of synthetic embryos is throwing into question our understanding of what a human embryo even is. “Is it the thing that is only generated from the fusion of a sperm and an egg?” Naomi Moris, a developmental biologist at the Crick Institute in London, said to me a couple of years ago. “Is it something to do with the cell types it possesses, or the [shape] of the structure?”

The authors of the new MIT Technology Review piece also point out that such bodyoids could also help speed scientific and medical research.

At the moment, most drug research must be conducted in lab animals before clinical trials can start. But nonhuman animals may not respond the same way people do, and the vast majority of treatments that look super-promising in mice fail in humans. Such research can feel like a waste of both animal lives and time.

Scientists have been working on solutions to these problems, too. Some are creating “organs on chips”—miniature collections of cells organized on a small piece of polymer that may resemble full-size organs and can be used to test the effects of drugs.

Others are creating digital representations of human organs for the same purpose. Such digital twins can be extensively modeled, and can potentially be used to run clinical trials in silico.

Both of these approaches seem somehow more palatable to me, personally, than running experiments on a human created without the capacity to think or feel pain. The idea reminds me of the recent novel Tender Is the Flesh by Agustina Bazterrica, in which humans are bred for consumption. In the book, their vocal cords are removed so that others do not have to hear them scream.

When it comes to real-world biotechnology, though, our feelings about what is “acceptable” tend to shift. In vitro fertilization was demonized when it was first developed, for instance, with opponents arguing that it was “unnatural,” a “perilous insult,” and “the biggest threat since the atom bomb.” It is estimated that more than 12 million people have been born through IVF since Louise Brown became the first “test tube baby” 46 years ago. I wonder how we’ll all feel about bodyoids 46 years from now.

This article first appeared in The Checkup, MIT Technology Review’s weekly biotech newsletter. To receive it in your inbox every Thursday, and read articles like this first, sign up here.

Ethically sourced “spare” human bodies could revolutionize medicine

Why do we hear about medical breakthroughs in mice, but rarely see them translate into cures for human disease? Why do so few drugs that enter clinical trials receive regulatory approval? And why is the waiting list for organ transplantation so long? These challenges stem in large part from a common root cause: a severe shortage of ethically sourced human bodies. 

It may be disturbing to characterize human bodies in such commodifying terms, but the unavoidable reality is that human biological materials are an essential commodity in medicine, and persistent shortages of these materials create a major bottleneck to progress.

This imbalance between supply and demand is the underlying cause of the organ shortage crisis, with more than 100,000 patients currently waiting for a solid organ transplant in the US alone. It also forces us to rely heavily on animals in medical research, a practice that can’t replicate major aspects of human physiology and makes it necessary to inflict harm on sentient creatures. In addition, the safety and efficacy of any experimental drug must still be confirmed in clinical trials on living human bodies. These costly trials risk harm to patients, can take a decade or longer to complete, and make it through to approval less than 15% of the time. 

There might be a way to get out of this moral and scientific deadlock. Recent advances in biotechnology now provide a pathway to producing living human bodies without the neural components that allow us to think, be aware, or feel pain. Many will find this possibility disturbing, but if researchers and policymakers can find a way to pull these technologies together, we may one day be able to create “spare” bodies, both human and nonhuman.

These could revolutionize medical research and drug development, greatly reducing the need for animal testing, rescuing many people from organ transplant lists, and allowing us to produce more effective drugs and treatments. All without crossing most people’s ethical lines.

Bringing technologies together

Although it may seem like science fiction, recent technological progress has pushed this concept into the realm of plausibility. Pluripotent stem cells, one of the earliest cell types to form during development, can give rise to every type of cell in the adult body. Recently, researchers have used these stem cells to create structures that seem to mimic the early development of actual human embryos. At the same time, artificial uterus technology is rapidly advancing, and other pathways may be opening to allow for the development of fetuses outside of the body. 

Such technologies, together with established genetic techniques to inhibit brain development, make it possible to envision the creation of “bodyoids”—a potentially unlimited source of human bodies, developed entirely outside of a human body from stem cells, that lack sentience or the ability to feel pain.

There are still many technical roadblocks to achieving this vision, but we have reason to expect that bodyoids could radically transform biomedical research by addressing critical limitations in the current models of research, drug development, and medicine. Among many other benefits, they would offer an almost unlimited source of organs, tissues, and cells for use in transplantation.

It could even be possible to generate organs directly from a patient’s own cells, essentially cloning someone’s biological material to ensure that transplanted tissues are a perfect immunological match and thus eliminating the need for lifelong immunosuppression. Bodyoids developed from a patient’s cells could also allow for personalized screening of drugs, allowing physicians to directly assess the effect of different interventions in a biological model that accurately reflects a patient’s own personal genetics and physiology. We can even envision using animal bodyoids in agriculture, as a substitute for the use of sentient animal species. 

Of course, exciting possibilities are not certainties. We do not know whether the embryo models recently created from stem cells could give rise to living people or, thus far, even to living mice. We do not know when, or whether, an effective technique will be found for successfully gestating human bodies entirely outside a person. We cannot be sure whether such bodyoids can survive without ever having developed brains or the parts of brains associated with consciousness, or whether they would still serve as accurate models for living people without those brain functions.

Even if it all works, it may not be practical or economical to “grow” bodyoids, possibly for many years, until they can be mature enough to be useful for our ends. Each of these questions will require substantial research and time. But we believe this idea is now plausible enough to justify discussing both the technical feasibility and the ethical implications. 

Ethical considerations and societal implications

Bodyoids could address many ethical problems in modern medicine, offering ways to avoid unnecessary pain and suffering. For example, they could offer an ethical alternative to the way we currently use nonhuman animals for research and food, providing meat or other products with no animal suffering or awareness. 

But when we come to human bodyoids, the issues become harder. Many will find the concept grotesque or appalling. And for good reason. We have an innate respect for human life in all its forms. We do not allow broad research on people who no longer have consciousness or, in some cases, never had it. 

At the same time, we know much can be gained from studying the human body. We learn much from the bodies of the dead, which these days are used for teaching and research only with consent. In laboratories, we study cells and tissues that were taken, with consent, from the bodies of the dead and the living.

Recently we have even begun using for experiments the “animated cadavers” of people who have been declared legally dead, who have lost all brain function but whose other organs continue to function with mechanical assistance. Genetically modified pig kidneys have been connected to, or transplanted into, these legally dead but physiologically active cadavers to help researchers determine whether they would work in living people

In all these cases, nothing was, legally, a living human being at the time it was used for research. Human bodyoids would also fall into that category. But there are still a number of issues worth considering. The first is consent: The cells used to make bodyoids would have to come from someone, and we’d have to make sure that this someone consented to this particular, likely controversial, use. But perhaps the deepest issue is that bodyoids might diminish the human status of real people who lack consciousness or sentience.

Thus far, we have held to a standard that requires us to treat all humans born alive as people, entitled to life and respect. Would bodyoids—created without pregnancy, parental hopes, or indeed parents—blur that line? Or would we consider a bodyoid a human being, entitled to the same respect? If so, why—just because it looks like us? A sufficiently detailed mannequin can meet that test. Because it looks like us and is alive? Because it is alive and has our DNA? These are questions that will require careful thought. 

A call to action

Until recently, the idea of making something like a bodyoid would have been relegated to the realms of science fiction and philosophical speculation. But now it is at least plausible—and possibly revolutionary. It is time for it to be explored. 

The potential benefits—for both human patients and sentient animal species—are great. Governments, companies, and private foundations should start thinking about bodyoids as a possible path for investment. There is no need to start with humans—we can begin exploring the feasibility of this approach with rodents or other research animals. 

As we proceed, the ethical and social issues are at least as important as the scientific ones. Just because something can be done does not mean it should be done. Even if it looks possible, determining whether we should make bodyoids, nonhuman or human, will require considerable thought, discussion, and debate. Some of that will be by scientists, ethicists, and others with special interest or knowledge. But ultimately, the decisions will be made by societies and governments. 

The time to start those discussions is now, when a scientific pathway seems clear enough for us to avoid pure speculation but before the world is presented with a troubling surprise. The announcement of the birth of Dolly the cloned sheep back in the 1990s launched a hysterical reaction, complete with speculation about armies of cloned warrior slaves. Good decisions require more preparation.

The path toward realizing the potential of bodyoids will not be without challenges; indeed, it may never be possible to get there, or even if it is possible, the path may never be taken. Caution is warranted, but so is bold vision; the opportunity is too important to ignore.

Carsten T. Charlesworth is a postdoctoral fellow at the Institute of Stem Cell Biology and Regenerative Medicine (ISCBRM) at Stanford University.

Henry T. Greely is the Deane F. and Kate Edelman Johnson Professor of Law and director of the Center for Law and the Biosciences at Stanford University.

Hiromitsu Nakauchi is a professor of genetics and an ISCBRM faculty member at Stanford University and a distinguished university professor at the Institute of Science Tokyo.