{"id":54656,"date":"2015-03-09T12:00:06","date_gmt":"2015-03-09T12:00:06","guid":{"rendered":"https:\/\/www.transcend.org\/tms\/?p=54656"},"modified":"2015-05-05T21:26:01","modified_gmt":"2015-05-05T20:26:01","slug":"engineering-the-perfect-baby","status":"publish","type":"post","link":"https:\/\/www.transcend.org\/tms\/2015\/03\/engineering-the-perfect-baby\/","title":{"rendered":"Engineering the Perfect Baby"},"content":{"rendered":"

Scientists are developing ways to edit the DNA of tomorrow\u2019s children. Should they stop before it\u2019s too late?<\/em><\/p>\n

\"Credit:<\/a>

Credit: Illustration by Javier Ja\u00e9n<\/p><\/div>\n

5 Mar 2015 – <\/em>If anyone had devised a way to create a genetically engineered baby, I figured George Church would know about it.<\/p>\n

At his labyrinthine laboratory on the Harvard Medical School campus, you can find researchers giving E. Coli <\/em>a novel genetic code never seen in nature. Around another bend, others are carrying out a plan to use DNA engineering to resurrect the woolly mammoth. His lab, Church likes to say, is the center of a new technological genesis\u2014one in which man rebuilds creation to suit himself.<\/p>\n

When I visited the lab last June, Church proposed that I speak to a young postdoctoral scientist named Luhan Yang, a Harvard recruit from Beijing who\u2019d been a key player in developing a new, powerful technology for editing DNA called CRISPR-Cas9. With Church, Yang had founded a small company to engineer the genomes of pigs and cattle, sliding in beneficial genes and editing away bad ones.<\/p>\n

As I listened to Yang, I waited for a chance to ask my real questions: Can any of this be done to human beings? Can we improve the human gene pool? The position of much of mainstream science has been that such meddling would be unsafe, irresponsible, and even impossible. But Yang didn\u2019t hesitate. Yes, of course, she said. In fact, the Harvard laboratory had a project to determine how it could be achieved. She flipped open her laptop to a PowerPoint slide titled \u201cGermline Editing Meeting.\u201d<\/p>\n

Here it was: a technical proposal to alter human heredity.<\/p>\n

\u201cGerm line\u201d is biologists\u2019 jargon for the egg and sperm, which combine to form an embryo. By editing the DNA of these cells or the embryo itself, it could be possible to eliminate disease genes and to pass those genetic fixes on to future generations. Such a technology could be used to rid families of scourges like cystic fibrosis. It might also be possible to install genes that offer lifelong protection against infection, Alzheimer\u2019s, and, Yang told me, maybe the effects of aging. These would be history-making medical advances that could be as important to this century as vaccines were to the last.<\/p>\n

That\u2019s the promise. The fear is that germ line engineering is a path toward a dystopia of super people and designer babies for those who can afford it. Want a child with blue eyes and blond hair? Why not design a highly intelligent group of people who could be tomorrow\u2019s leaders and scientists?<\/p>\n

Just three years after its initial development, CRISPR technology is already widely used by biologists as a kind of search-and-replace tool to alter DNA, even down to the level of a single letter. It\u2019s so precise that it\u2019s widely expected to turn into a promising new approach for gene therapy treatment in people with devastating illnesses. The idea is that physicians could directly correct a faulty gene, say, in the blood cells of a patient with sickle-cell anemia (see \u201cGenome Surgery<\/a>\u201d). But that kind of gene therapy wouldn\u2019t affect germ cells, and the changes in the DNA wouldn\u2019t get passed to future generations.<\/p>\n

In contrast, the genetic changes created by germ line engineering would be passed on, and that\u2019s what has always made the idea seem so objectionable. So far, caution and ethical concerns have had the upper hand. A dozen countries, not including the United States, have banned germ line engineering, and scientific societies have unanimously concluded that it would be too risky to do. The European Union\u2019s convention on human rights and biomedicine says tampering with the gene pool would be a crime against \u201chuman dignity\u201d and human rights.<\/p>\n

But all these declarations were made before it was actually feasible to precisely engineer the germ line. Now, with CRISPR, it is possible.<\/p>\n

The experiment Yang described, though not simple, would go like this: The researchers hoped to obtain, from a hospital in New York, the ovaries of a woman undergoing surgery for ovarian cancer, caused by a mutation in a gene called BRCA1. Working with another Harvard laboratory, that of antiaging specialist David Sinclair<\/a>, they would extract immature egg cells that could be coaxed to grow and divide in the laboratory. Yang would use CRISPR in these cells to correct the DNA of the BRCA1 gene. The objective is to create a viable egg without the genetic error that caused the woman\u2019s cancer.<\/p>\n

As with several other scientists whom I\u2019d asked about human germ line engineering, Yang stopped replying to my questions, so it\u2019s hard to know if the experiment she described is occurring, canceled, or pending publication. Church, in a phone call, termed it a \u201cnon-project,\u201d at least until it has generated a publishable result, though Sinclair said a collaboration between the labs is ongoing. (After this story was published, Yang called to say she had not worked on the experiment for several months.) Regardless of the fate of that particular experiment, human germ line engineering has become a burgeoning research concept. At least one other center in Boston is working on it, as are scientists in China, in the U.K., and at a biotechnology company called OvaScience, based in Cambridge, Massachusetts, that boasts some of the world\u2019s leading fertility doctors on its advisory board.<\/p>\n

The objective of these groups is to demonstrate that it\u2019s possible to produce children free of specific genes that cause inherited disease. If it\u2019s possible to correct the DNA in a woman\u2019s egg, or a man\u2019s sperm, those cells could be used in an in vitro fertilization (IVF) clinic to produce an embryo and then a child. It might also be possible to directly edit the DNA of an early-stage IVF embryo using CRISPR. Several people interviewed by MIT Technology Review<\/em> said that such experiments had already been carried out in China and that results describing edited embryos were pending publication. These people didn\u2019t wish to comment publicly because the papers are under review.<\/p>\n

All this means that germ line engineering is much farther along than anyone imagined. \u201cWhat you are talking about is a major issue for all humanity,\u201d says Merle Berger, one of the founders of Boston IVF, a network of fertility clinics that is among the largest in the world and helps more than a thousand women get pregnant each year. \u201cIt would be the biggest thing that ever happened in our field,\u201d he says. Berger predicts that repairing genes for serious inherited disease will win wide public acceptance, but beyond that, the technology would cause a public uproar because \u201ceveryone would want the perfect child\u201d and it could lead to picking and choosing eye color and eventually intelligence. \u201cThese are things we talk about all the time. But we have never had the opportunity to do it.\u201d<\/p>\n

Editing Embryos<\/strong><\/p>\n

How easy would it be to edit a human embryo using CRISPR? Very easy, experts say. \u201cAny scientist with molecular biology skills and knowledge of how to work with [embryos] is going to be able to do this,\u201d says Jennifer Doudna, a University of California, Berkeley, biologist who in 2012 codiscovered how to use CRISPR to edit genes.<\/p>\n

To find out how it could be done, I visited the lab of Guoping Feng, a biologist at MIT\u2019s McGovern Institute for Brain Research, where a colony of marmoset monkeys is being established with the aim of using CRISPR to create accurate models of human brain diseases. To create the models, Feng will edit the DNA of embryos and then transfer them into female marmosets to produce live monkeys. One gene Feng hopes to alter is SHANK3. The gene is involved in how neurons communicate and, when it\u2019s damaged in children, is known to cause autism.<\/p>\n

Feng said that before CRISPR, it was not possible to introduce precise changes into a primate\u2019s DNA, but last year the first gene-edited monkeys were born in Kunming, China (see \u201cMonkeys Modified with Genome Editing<\/a>\u201d). The CRISPR system includes a gene-snipping enzyme and a guide molecule that can be programmed to target unique combinations of the DNA letters, A, G, C, and T; get these ingredients into a cell and they will cut and modify the targeted letters.<\/p>\n

But CRISPR is not perfect\u2014and it would be a very haphazard way to edit human embryos, as Feng\u2019s efforts to create gene-edited marmosets show. To employ the CRISPR system in the monkeys, his students simply inject the chemicals into a fertilized egg, which is known as a zygote\u2014the stage just before it starts dividing.<\/p>\n

Feng said the efficiency with which CRISPR can delete or disable a gene in a zygote is about 40 percent, whereas making specific edits, or swapping DNA letters, should work less frequently\u2014more like 20 percent of the time. Like a person, a monkey has two copies of most genes, one from each parent. Sometimes both copies get edited, but sometimes just one does, or neither. Only about half the embryos will lead to live birth, and of those that do, many could contain a mixture of cells with edited DNA and cells without. If you add up the odds, you find you\u2019d need to edit about 20 embryos to get a live monkey with the edit you want. That\u2019s not an insurmountable problem for Feng, since the MIT breeding colony will give him access to many monkey eggs and he\u2019ll be able to generate many embryos.<\/p>\n

However, it presents obvious problems for using the same process on humans. Putting the ingredients of CRISPR into a human embryo would be scientifically trivial. But it wouldn\u2019t be practical for much just yet. This is one reason that many scientists view such an experiment\u2014whether or not it has really occurred in China\u2014with scorn, and see it more as a provocative bid to grab attention than real science. Rudolf Jaenisch, an MIT biologist who works across the street from Feng, and who in the 1970s created the first gene-modified mice, called attempts to edit human embryos \u201ctotally premature.\u201d He said he hoped these papers would be rejected and never published. \u201cIt\u2019s just a sensational thing that will stir things up. We know it\u2019s possible, but is it of practical use? I kind of doubt it,\u201d said Jaenisch.<\/p>\n

But Feng told me he approves of the idea of germ line engineering. Isn\u2019t the goal of medicine to reduce suffering? Considering the state of the technology, however, he thinks actual gene-edited humans are \u201c10 to 20 years away.\u201d Among other problems, CRISPR can introduce off-target effects or change bits of the genome far from where scientists had intended. Any human embryo altered with CRISPR today would carry the risk that its genome had been changed in unexpected ways. But, Feng said, such problems may eventually be ironed out and edited people will be born. \u201cTo me, it\u2019s possible in the long run to dramatically improve health, lower costs. It\u2019s a kind of prevention,\u201d he said. \u201cIt\u2019s hard to predict the future, but correcting disease risks is definitely a possibility and should be supported. I think it will be a reality.\u201d<\/p>\n

Editing Eggs<\/strong><\/p>\n

Elsewhere in Boston, scientists are exploring a different approach to engineering the germ line that is technically more demanding but likely more powerful. This strategy combines CRISPR with unfolding discoveries related to stem cells. Scientists at several centers, including Church\u2019s, think they will soon be able to use stem cells to produce eggs and sperm in the laboratory. Unlike an embryo, stem cells can be grown and multiplied. Thus they could offer a vastly improved way to create edited offspring with CRISPR. The recipe goes like this: First, edit the genes of the stem cells. Second, turn them into an egg or sperm. Third, produce an offspring.<\/p>\n

Some investors got an early view of the technique on December 17 at the Benjamin Hotel in Manhattan during commercial presentations by OvaScience, a company that was founded four years ago to commercialize the scientific work of Harvard\u2019s Sinclair and Jonathan Tilly, an expert on egg stem cells and the chairman of the biology department at Northeastern University (see \u201c10 Breakthrough Technologies 2012: Egg Stem Cells\u201d<\/a>). The company\u2019s presentations were part of its successful effort to raise $132 million in new capital during January.<\/p>\n

During the meeting, Sinclair, a velvet-voiced Australian whom Time<\/em> last year named one of the \u201c100 Most Influential People in the World,\u201d took the podium and provided Wall Street with a peek at what he called \u201ctruly world-changing\u201d developments. These, he said, would cause people to look back at this moment in time and recognize it as a new chapter in \u201chow humans control their bodies,\u201d because it would let parents determine \u201cwhen and how they have children and how healthy those children are actually going to be.\u201d<\/p>\n

Ovascience has been collecting, and studying, what it believes are egg stem cells from the outer layer of women\u2019s ovaries. The company has not yet perfected its stem cell technology\u2014it has not reported that the eggs it grows in the lab are viable\u2014but Sinclair predicted that functional eggs were \u201ca when, and not an if.\u201d Once the technology works, he said, infertile women will be able to produce hundreds of eggs, and maybe hundreds of embryos. Using DNA sequencing to analyze their genes, they could pick among them for the healthiest ones.<\/p>\n

Genetically improved children may also be possible. Sinclair told the investors that he was trying to alter the DNA of these egg stem cells using gene editing, work he later told me he was doing with Church\u2019s lab. \u201cWe think the new technologies with genome editing will allow it to be used on individuals who aren\u2019t just interested in using IVF to have children but have healthier children as well, if there is a genetic disease in their family,\u201d Sinclair told the investors. He gave the example of Huntington\u2019s disease, caused by a gene that will trigger a fatal brain condition even in someone who inherits only one copy of it. Sinclair said gene editing could be used to remove the lethal gene defect from an egg cell. He described his goal, and that of OvaScience, as being to \u201ccorrect those mutations before we generate your child. It\u2019s still experimental, but there is no reason to expect it won\u2019t be possible in coming years.\u201d<\/p>\n

\"baby_chartx392_1<\/a>Sinclair spoke to me briefly on the phone as he travled across snowed-in Boston in a cab, but later referred my questions to OvaScience. When I contacted OvaScience, Cara Mayfield, a spokeswoman, said its executives could not comment because of their travel schedules but confirmed that the company was working on treating inherited disorders with gene editing. What was surprising to me is that OvaScience\u2019s research in \u201ccrossing the germ line,\u201d as critics of human engineering sometimes put it, has generated scarcely any notice. In December 2013, OvaScience even announced it was putting $1.5 million into a joint venture with a synthetic biology company called Intrexon, whose R&D objectives include gene-editing egg stem cells to \u201cprevent the propagation\u201d of human disease \u201cin future generations.\u201d<\/p>\n

When I reached Tilly at Northeastern, he laughed when I told him what I was calling about. \u201cIt\u2019s going to be a hot-button issue,\u201d he said. Tilly also said his lab was trying to edit egg cells with CRISPR \u201cright now\u201d to rid them of an inherited genetic disease that he didn\u2019t want to name. Tilly emphasized that there are \u201ctwo pieces of the puzzle\u201d\u2014one being stem cells and the other gene editing. The ability to create large numbers of egg stem cells is critical, because only with sizable quantities can genetic changes, using CRISPR, be stably introduced, characterized using DNA sequencing, and carefully studied to check for mistakes before producing an egg.<\/p>\n

Tilly predicted that the whole end-to-end technology\u2014cells to stem cells, stem cells to sperm or egg and then to offspring\u2014would end up being worked out first in animals, such as cattle, either by his lab or by companies such as eGenesis, the spin-off from the Church lab working on livestock. But he isn\u2019t sure what the next step should be with edited human eggs. You wouldn\u2019t \u201cwilly nilly\u201d want to fertilize one, he said. You\u2019d be making a potential human being. And doing that would raise questions he\u2019s not sure he can answer. He told me, \u201c\u2018Can you do it?\u2019 is one thing. If you can, then the most important questions come up. \u2018Would you do it? Why would you want to do it? What is the purpose?\u2019 As scientists we want to know if it\u2019s feasible, but then we get into the bigger questions, and it\u2019s not a science question, it\u2019s a society question.\u201d<\/p>\n

Improving Humans<\/strong><\/p>\n

If germ line engineering becomes part of medical practice, it could lead to transformative changes in human well-being, with consequences to people\u2019s life span, identity, and economic output. But it would create ethical dilemmas and social challenges. What if these improvements were available only to the richest societies, or the richest people? An in vitro fertility procedure costs about $20,000 in the United States. Add genetic testing and egg donation or a surrogate mother and the price soars towards $100,000.<\/p>\n

Others believe the idea\u2019s downfall is that medical reasons to follow through on it are lacking. Hank Greely, a law professor and ethicist at Stanford University, says proponents \u201ccan\u2019t really say what it is good for.\u201d The problem, says Greely, is that it\u2019s already possible to test the DNA of IVF embryos and pick healthy ones, a process that adds about $4,000 to the cost of a fertility procedure. A man with Huntington\u2019s, for instance, could have his sperm used to fertilize a dozen of his partner\u2019s eggs. Half those embryos would not have the Huntington\u2019s gene, and those could be used to begin a pregnancy.<\/p>\n

Indeed, some people are adamant that germ line engineering is being pushed ahead with \u201cfalse arguments.\u201d That is the view of Edward Lanphier, CEO of Sangamo Biosciences, a California biotechnology company that is using another gene editing technique, called zinc finger nucleases, to try to treat HIV in adults by altering their blood cells. \u201cWe\u2019ve looked at [germ line engineering] for a disease rationale, and there is none,\u201d he says. \u201cYou can do it. But there really isn\u2019t a medical reason. People say, well, we don\u2019t want children born with this, or born with that\u2014but it\u2019s a completely false argument and a slippery slope toward much more unacceptable uses.\u201d<\/p>\n

Critics cite a host of fears. Children would be the subject of experiments. Parents would be influenced by genetic advertising from IVF clinics. Germ line engineering would lead to \u201cpositive eugenics,\u201d encouraging the spread of allegedly superior genes. And it would affect people not yet born, without their being able to agree to it. The American Medical Association, for instance, holds the position that germ line engineering shouldn\u2019t be done \u201cat this time\u201d because it \u201caffects the welfare of future generations\u201d and could cause \u201cunpredictable and irreversible results.\u201d But like a lot of official statements against germ line engineering, the AMA\u2019s, which was last updated in 1996<\/a>, predates today\u2019s technology. \u201cA lot of people just agreed to these statements. It wasn\u2019t hard to renounce something that you couldn\u2019t do,\u201d says Greely.<\/p>\n

Others predict that hard-to-oppose medical uses will be identified. A couple might have several genetic diseases at once, and not find a suitable embryo. Treating infertility is another possibility. Some men don\u2019t produce any sperm, a condition called azoospermia. One cause is a genetic defect in which a region of about one to six million DNA letters is missing from their Y chromosome. It might be possible, says Werner Neuhausser, a young Austrian doctor who splits his time between Boston IVF, the fertility-clinic network, and Harvard\u2019s Stem Cell Institute, to take a skin cell from such a man, turn it into a stem cell, repair the DNA, and then make sperm. \u201cThat will change medicine forever, right? You could cure infertility, that is for sure,\u201d says Neuhausser.<\/p>\n

I spoke with Church several times by telephone over the last few months, and he told me what\u2019s driving everything is the \u201cincredible specificity\u201d of CRISPR. Although not all the details have been worked out, he thinks the technology could replace DNA letters essentially without side effects. He says this is what makes it \u201ctempting to use.\u201d Church says his laboratory is focused mostly on experiments in engineering animals. He added that his lab would not make or edit human embryos, calling such a step \u201cnot our style.\u201d<\/p>\n

What is Church\u2019s style is human enhancement. And he\u2019s been making a broad case that CRISPR can do more than eliminate disease genes. It can lead to augmentation. At meetings of groups of people known as \u201ctranshumanists,\u201d who are interested in next steps for human evolution, Church likes to show a slide on which he lists naturally occurring variants of around 10 genes that, when people are born with them, give them extraordinary qualities or resistance to disease. One makes your bones so hard they\u2019ll break a surgical drill. Another drastically cuts the risk of heart attacks. And a variant of the gene for the amyloid precursor protein, or APP, was found by Icelandic researchers to protect against Alzheimer\u2019s. People with it never get dementia and remain sharp into old age.<\/p>\n

Church thinks CRISPR could be used to provide people with favorable versions of genes, making DNA edits that would act as vaccines\u2014not against viruses but against some of the most common diseases we face today. Although Church told me anything \u201cedgy\u201d should only be done to adults who can agree to it, it\u2019s obvious to him that the earlier such interventions occur, the better.<\/p>\n

Church tends to dodge questions about genetically modified babies. The idea of improving the human species, he wrote in the introduction to Regenesis<\/em>, his 2012 book on synthetic biology\u2014whose cover was a painting by Eustache Le Sueur of a bearded God creating the world\u2014has always had \u201cenormously bad press.\u201d But that\u2019s ultimately what he\u2019s suggesting: enhancements in the form of protective genes. \u201cAn argument will be made that the ultimate prevention is that the earlier you go, the better the prevention,\u201d he told an audience at MIT\u2019s Media Lab last spring. \u201cI do think it\u2019s the ultimate preventive, if<\/em> we get to the point where it\u2019s very inexpensive, extremely safe, and very predictable.\u201d Church, who has a less cautious side, proceeded to tell the audience that he thought changing genes \u201cis going to get to the point where it\u2019s like you are doing the equivalent of cosmetic surgery.\u201d<\/p>\n

Some thinkers have concluded that we should not pass up the chance to make improvements to our species. \u201cThe human genome is not perfect,\u201d says John Harris, a bioethicist at Manchester University, in the U.K. \u201cIt\u2019s ethically imperative to positively support this technology.\u201d By some measures, public opinion in the U.S. is not particularly negative toward the idea. A Pew Research survey carried out last August found that 46 percent of adults approved of genetic modification of babies to reduce the risk of serious diseases. (The same survey found that 83 percent said doing so to make a baby smarter would be \u201ctaking medical advances too far.\u201d)<\/p>\n

Other observers say higher IQ is exactly what we should be considering. Nick Bostrom, a philosopher at Oxford University best known for his 2014 book Superintelligence<\/em>, which raised alarms about the risks of artificial intelligence in computers, has also looked at whether humans could use reproductive technology to improve human intellect. Although the ways in which genes affect intelligence aren\u2019t well understood and there are far too many relevant genes to permit easy engineering, such realities don\u2019t dim speculation on the possibilities of high-tech eugenics.<\/p>\n

What if everyone could be a little bit smarter? Or a few people could be a lot smarter? Even a small number of \u201csuper-enhanced\u201d individuals, Bostrom wrote in a 2013 paper, could change the world through their creativity and discoveries, and through innovations that everyone else would use. In his view, genetic enhancement is as important an issue as climate change or long-range financial planning by nations, \u201csince human problem-solving ability is a factor in every challenge we face.\u201d<\/p>\n

To some scientists, the explosive advance of genetics and biotech means germ line engineering is inevitable. Of course, safety questions would be paramount. Before there\u2019s a genetically edited baby saying \u201cMama,\u201d there would have to be tests in rats, rabbits, and probably monkeys, to make sure they are normal. But ultimately, if the benefits seem to outweigh the risks, medicine would take the chance. \u201cIt was the same with IVF when it first happened,\u201d says Neuhausser. \u201cWe never really knew if that baby was going to be healthy at 40 or 50 years. But someone had to take the plunge.\u201d<\/p>\n

Wine Country<\/strong><\/p>\n

In January, on Saturday the 24th, around 20 scientists, ethicists, and legal experts traveled to Napa Valley, California, for a retreat among the vineyards at the Carneros Inn. They had been convened by Doudna, the Berkeley scientist who codiscovered how to edit genes with CRISPR. She had become aware, and concerned, that scientists were intent on crossing the germ line. Now she wanted to know: could they be stopped?<\/p>\n

\u201cWe as scientists have come to appreciate that [CRISPR] is incredibly powerful. But that swings both ways. We need to make sure that it\u2019s applied carefully,\u201d Doudna told me. \u201cThe issue is especially human germ line editing and the appreciation that this is now a capability in everyone\u2019s hands.\u201d<\/p>\n

At the meeting, along with ethicists like Greely, was Paul Berg, a Stanford biochemist known for having organized the Asilomar Conference in 1975, a historic forum at which biologists reached an agreement on how to safely proceed with recombinant DNA, the then newly discovered method of splicing DNA into bacteria.<\/p>\n

Should there be an Asilomar for germ line engineering? Doudna thinks so, but the prospects for reaching such a consensus these days seem unlikely. Biotechnology research is now global, employing millions of people. There\u2019s no single authority that speaks for science and no easy way to put the genie back in the bottle. Doudna told me that she hoped at least American scientists might come to a consensus that germ line research should be paused. Some people at the meeting said they would be signing a statement they would publish in a high-profile scientific journal, outlining their concerns. Doudna says she hopes that if U.S. scientists make a joint statement, it might influence researchers elsewhere in the world to cease their work.<\/p>\n

Doudna believes a self-imposed pause should apply not only to altering embryos but also to using CRISPR to alter human eggs or sperm\u2014as researchers at Harvard, Northeastern, and OvaScience are doing. \u201cI don\u2019t feel that those experiments are appropriate to do right now in human cells that could turn into a person,\u201d she told me. \u201cI feel that the research that needs to be done right now is to understand safety, efficacy, and delivery. And I think those experiments can be done in nonhuman systems. I would like to see a lot more work done before it\u2019s done for germ line editing. I would favor a very cautious approach.\u201d<\/p>\n

Not everyone agrees germ line engineering is such a big worry, or that experiments should be padlocked. Greely notes that in the United States, there are piles of regulations to stand in the way of lab science morphing into a genetically modified baby anytime soon. \u201cI would not want to use safety as an excuse for a non-safety-based ban,\u201d says Greely, who says he pushed back against talk of a moratorium. But Greely also says he agreed to sign Doudna\u2019s letter, which now reflects the consensus of the group. \u201cAlthough I don\u2019t view this as a crisis moment, I think it\u2019s probably about time for us to have this discussion,\u201d he says.<\/p>\n

As news has spread of germ line experiments, some biotechnology companies working on CRISPR have realized they will have to take a stand. Nessan Bermingham is CEO of Intellia Therapeutics, a Boston startup, which raised $15 million last year to develop CRISPR into gene therapy treatments for adults or children. He says germ line engineering \u201cis not on our commercial radar,\u201d and he suggests that his company could use its patents to prevent anyone from commercializing it. \u201cThe technology is in its infancy,\u201d he says. \u201cIt is not appropriate for people to even be contemplating germ line applications.\u201d<\/p>\n

Bermingham told me he never imagined he\u2019d have to be taking a position on genetically modified babies so soon. Rewriting human heredity has always been a theoretical possibility. Suddenly it\u2019s a real one. But wasn\u2019t the point always to understand and control our own biology\u2014to become masters over the processes that created us?<\/p>\n

Doudna says she is also thinking about these issues. \u201cIt cuts to the core of who we are as people, and it makes you ask if humans should be exercising that kind of power. There are moral and ethical issues, but one of the profound questions is just the appreciation that if germ line editing is conducted in humans, that is changing human evolution,\u201d Doudna told me. One reason she feels the research should stop is to give scientists a chance to spend more time explaining what their next steps could be. \u201cMost of the public,\u201d she says, \u201cdoes not appreciate what is coming.\u201d<\/p>\n

________________________<\/p>\n

Antonio Regalado – I am the senior editor for biomedicine for <\/em>MIT Technology Review. I look for stories about how technology is changing medicine and biomedical research. Before joining <\/em>MIT Technology Review in July 2011, I lived in S\u00e3o Paulo, Brazil, where I wrote about science, technology, and politics in Latin America for <\/em>Science and other publications. From 2000 to 2009, I was the science reporter at the <\/em>Wall Street Journal and later a foreign correspondent.<\/em><\/p>\n

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Scientists are developing ways to edit the DNA of tomorrow\u2019s children. Should they stop before it\u2019s too late? \u201cYou can do it. But there really isn\u2019t a medical reason. People say, well, we don\u2019t want children born with this, or born with that\u2014but it\u2019s a completely false argument and a slippery slope toward much more unacceptable uses.\u201d<\/p>\n","protected":false},"author":4,"featured_media":0,"comment_status":"open","ping_status":"open","sticky":false,"template":"","format":"standard","meta":{"footnotes":""},"categories":[140],"tags":[],"class_list":["post-54656","post","type-post","status-publish","format-standard","hentry","category-organic-gmo-genetic-engineering"],"_links":{"self":[{"href":"https:\/\/www.transcend.org\/tms\/wp-json\/wp\/v2\/posts\/54656","targetHints":{"allow":["GET"]}}],"collection":[{"href":"https:\/\/www.transcend.org\/tms\/wp-json\/wp\/v2\/posts"}],"about":[{"href":"https:\/\/www.transcend.org\/tms\/wp-json\/wp\/v2\/types\/post"}],"author":[{"embeddable":true,"href":"https:\/\/www.transcend.org\/tms\/wp-json\/wp\/v2\/users\/4"}],"replies":[{"embeddable":true,"href":"https:\/\/www.transcend.org\/tms\/wp-json\/wp\/v2\/comments?post=54656"}],"version-history":[{"count":0,"href":"https:\/\/www.transcend.org\/tms\/wp-json\/wp\/v2\/posts\/54656\/revisions"}],"wp:attachment":[{"href":"https:\/\/www.transcend.org\/tms\/wp-json\/wp\/v2\/media?parent=54656"}],"wp:term":[{"taxonomy":"category","embeddable":true,"href":"https:\/\/www.transcend.org\/tms\/wp-json\/wp\/v2\/categories?post=54656"},{"taxonomy":"post_tag","embeddable":true,"href":"https:\/\/www.transcend.org\/tms\/wp-json\/wp\/v2\/tags?post=54656"}],"curies":[{"name":"wp","href":"https:\/\/api.w.org\/{rel}","templated":true}]}}