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venerdì 6 marzo 2015


Scientists are developing ways to edit the DNA of tomorrow’s children. Should they stop before it’s too late?

At his labyrinthine laboratory on the Harvard Medical School campus, you can find researchers giving E. Coli 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, George Church likes to say, is the center of a new technological genesis—one in which man rebuilds creation to suit himself.

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’d been a key player in developing a new, powerful technology for editing DNA called CRISPR-Cas9. With Church, Yang had founded a company called eGenesis to engineer the genomes of pigs and cattle, sliding in beneficial genes and editing away bad ones.

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’t hesitate. Yes, of course, she said. In fact, the laboratory had a project to determine how it could be achieved. She flipped open her laptop to a PowerPoint slide titled “Germline Editing Meeting.” 

Here it was: a technical proposal to alter human heredity.

Germ line” is biologists’ 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’s, 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.

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.

That’s 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’s leaders and scientists?

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’s so precise that it’s 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 “Genome Surgery”). But that kind of gene therapy wouldn’t affect germ cells, and the changes in the DNA wouldn’t get passed to future generations.

In contrast, the genetic changes created by germ line engineering would be passed on, and that’s 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’s convention on human rights and biomedicine says tampering with the gene pool would be a crime against “human dignity” and human rights.

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

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, 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’s cancer.

As with several other scientists whom I’d asked about human germ line engineering, Yang stopped replying to my questions, so it’s hard to know if the experiment she described is occurring, canceled, or pending publication. Church, in a phone call, termed it a “non-project,” 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’s leading fertility doctors on its advisory board.

The objective of these groups is to demonstrate that it’s possible to produce children free of specific genes that cause inherited disease. If it’s possible to correct the DNA in a woman’s egg, or a man’s 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 said that such experiments had already been carried out in China and that results describing edited embryos were pending publication. These people didn’t wish to comment publicly because the papers are under review.

All this means that germ line engineering is much farther along than anyone imagined. “What you are talking about is a major issue for all humanity,” 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. “It would be the biggest thing that ever happened in our field,” 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 “everyone would want the perfect child” and it could lead to picking and choosing eye color and eventually intelligence. “These are things we talk about all the time. But we have never had the opportunity to do it.”

Editing Embryos

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

To find out how it could be done, I visited the lab of Guoping Feng, a biologist at MIT’s 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’s damaged in children, is known to cause autism.

“You can do it. But there really isn’t a medical reason. People say, well, we don’t want children born with this, or born with that—but it’s a completely false argument and a slippery slope toward much more unacceptable uses.”

Feng said that before CRISPR, it was not possible to introduce precise changes into a primate’s DNA, but last year the first gene-edited monkeys were born in Kunming, China (see “Monkeys Modified with Genome Editing”). 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.

But CRISPR is not perfect—and it would be a very haphazard way to produce edited children, as Feng’s 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—the stage just before it starts dividing.

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, works less frequently—more 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 lead to live birth, and of those that do, many contain a mixture of cells with edited DNA and cells without. If you add up the odds, you find you’d need to edit about 20 embryos to get a live monkey with the edit you want. That’s not an insurmountable problem for Feng, since the MIT breeding colony will give him access to many monkey eggs and he’ll be able to generate many embryos.

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’t be practical for much just yet. This is one reason that many scientists view such an experiment—whether or not it has really occurred in China—with 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 “totally premature.” He said he hoped these papers would be rejected and never published. “It’s just a sensational thing that will stir things up. We know it’s possible, but is it of practical use? I kind of doubt it,” said Jaenisch.

But Feng told me he approves of the idea of germ line engineering. Isn’t the goal of medicine to reduce suffering? Considering the state of the technology, however, he thinks actual gene-edited humans are “10 to 20 years away.” 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. “To me, it’s possible in the long run to dramatically improve health, lower costs. It’s a kind of prevention,” he said. “It’s hard to predict the future, but correcting disease risks is definitely a possibility and should be supported. I think it will be a reality.”

Editing Eggs

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’s, 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.

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’s Sinclair and Jonathan Tilly, an expert on egg stem cells and the chairman of the biology department at Northeastern University (see “10 Breakthrough Technologies 2012: Egg Stem Cells”). The company’s presentations were part of its successful effort to raise $132 million in new capital during January.

During the meeting, Sinclair, a velvet-voiced Australian whom Time last year named one of the “100 Most Influential People in the World,” took the podium and provided Wall Street with a peek at what he called “truly world-changing” developments. These, he said, would cause people to look back at this moment in time and recognize it as a new chapter in “how humans control their bodies,” because it would let parents determine “when and how they have children and how healthy those children are actually going to be.”

Ovascience has been collecting, and studying, what it believes are egg stem cells from the outer layer of women’s ovaries. The company has not yet perfected its stem cell technology—it has not reported that the eggs it grows in the lab are viable—but Sinclair predicted that functional eggs were “a when, and not an if.” 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.

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’s lab. “We think the new technologies with genome editing will allow it to be used on individuals who aren’t just interested in using IVF to have children but have healthier children as well, if there is a genetic disease in their family,” Sinclair told the investors. He gave the example of Huntington’s 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 “correct those mutations before we generate your child. It’s still experimental, but there is no reason to expect it won’t be possible in coming years.” 

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’s research in “crossing the germ line,” 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 “prevent the propagation” of human disease “in future generations.”

When I reached Tilly at Northeastern, he laughed when I told him what I was calling about. “It’s going to be a hot-button issue,” he said. Tilly also said his lab was trying to edit egg cells with CRISPR “right now” to rid them of an inherited genetic disease that he didn’t want to name. Tilly emphasized that there are “two pieces of the puzzle”—one 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.

Tilly predicted that the whole end-to-end technology—cells to stem cells, stem cells to sperm or egg and then to offspring—would 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. But he isn’t sure what the next step should be with edited human eggs. You wouldn’t “willy nilly” want to fertilize one, he said. You’d be making a potential human being. And doing that would raise questions he’s not sure he can answer. He told me, “‘Can you do it?’ is one thing. If you can, then the most important questions come up. ‘Would you do it? Why would you want to do it? What is the purpose?’ As scientists we want to know if it’s feasible, but then we get into the bigger questions, and it’s not a science question, it’s a society question.”

Improving Humans

If germ line engineering becomes part of medical practice, it could lead to transformative changes in human well-being, with consequences to people’s 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.

Others believe the idea’s downfall is that medical reasons to follow through on it are lacking. Hank Greely, a law professor and ethicist at Stanford University, says proponents “can’t really say what it is good for.” The problem, says Greely, is that it’s 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’s, for instance, could have his sperm used to fertilize a dozen of his partner’s eggs. Half those embryos would not have the Huntington’s gene, and those could be used to begin a pregnancy.

Indeed, some people are adamant that germ line engineering is being pushed ahead with “false arguments.” 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. “We’ve looked at [germ line engineering] for a disease rationale, and there is none,” he says. “You can do it. But there really isn’t a medical reason. People say, well, we don’t want children born with this, or born with that—but it’s a completely false argument and a slippery slope toward much more unacceptable uses.”

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 “positive eugenics,” 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’t be done “at this time” because it “affects the welfare of future generations” and could cause “unpredictable and irreversible results.” But like a lot of official statements against germ line engineering, the AMA’s, which was last updated in 1996, predates today’s technology. “A lot of people just agreed to these statements. It wasn’t hard to renounce something that you couldn’t do,” says Greely.

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’t 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’s 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. “That will change medicine forever, right? You could cure infertility, that is for sure,” says Neuhausser.

I spoke with Church several times by telephone over the last few months, and he told me what’s driving everything is the “incredible specificity” 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 “tempting to use.” 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 “not our style.”

To some scientists, the explosive advance of genetics and biotech means germ line engineering is inevitable. Ultimately, if the benefits seem to outweigh the risks, medicine would take the chance.

What is Church’s style is human enhancement. And he’s 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 “transhumanists,” 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’ll 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’s. People with it never get dementia and remain sharp into old age.

Church thinks CRISPR could be used to provide people with favorable versions of genes, making DNA edits that would act as vaccines—not against viruses but against some of the most common diseases we face today. Although Church told me anything “edgy” should only be done to adults who can agree to it, it’s obvious to him that the earlier such interventions occur, the better.

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

Some thinkers have concluded that we should not pass up the chance to make improvements to our species. “The human genome is not perfect,” says John Harris, a bioethicist at Manchester University, in the U.K. “It’s ethically imperative to positively support this technology.” 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 “taking medical advances too far.”)

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, 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’t well understood and there are far too many relevant genes to permit easy engineering, such realities don’t dim speculation on the possibilities of high-tech eugenics.

What if everyone could be a little bit smarter? Or a few people could be a lot smarter? Even a small number of “super-enhanced” 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, “since human problem-solving ability is a factor in every challenge we face.”

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’s a genetically edited baby saying “Mama,” 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. “It was the same with IVF when it first happened,” says Neuhausser. “We never really knew if that baby was going to be healthy at 40 or 50 years. But someone had to take the plunge.”

Wine Country

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?

“We as scientists have come to appreciate that [CRISPR] is incredibly powerful. But that swings both ways. We need to make sure that it’s applied carefully,” Doudna told me. “The issue is especially human germ line editing and the appreciation that this is now a capability in everyone’s hands.”

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.

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’s 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.

Doudna believes a self-imposed pause should apply not only to altering embryos but also to using CRISPR to alter human eggs or sperm—as researchers at Harvard, Northeastern, and OvaScience are doing. “I don’t feel that those experiments are appropriate to do right now in human cells that could turn into a person,” she told me. “I 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’s done for germ line editing. I would favor a very cautious approach.”

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. “I would not want to use safety as an excuse for a non-safety-based ban,” says Greely, who says he pushed back against talk of a moratorium. But Greely also says he agreed to sign Doudna’s letter, which now reflects the consensus of the group. “Although I don’t view this as a crisis moment, I think it’s probably about time for us to have this discussion,” he says.

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 “is not on our commercial radar,” and he suggests that his company could use its patents to prevent anyone from commercializing it. “The technology is in its infancy,” he says. “It is not appropriate for people to even be contemplating germ line applications.”

Bermingham told me he never imagined he’d have to be taking a position on genetically modified babies so soon. Rewriting human heredity has always been a theoretical possibility. Suddenly it’s a real one. But wasn’t the point always to understand and control our own biology—to become masters over the processes that created us?

Doudna says she is also thinking about these issues. “It 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,” 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. “Most of the public,” she says, “does not appreciate what is coming.”

Il genetista dell’anno è George Church della Harvard Medical School, autore di "Regenesis. How Synthetic Biology will reinvent Nature and Ourselves".

Il libro, scritto insieme al giornalista Ed Regis, non passerà alla storia per l’affascinante argomento trattato – come la biologia sintetica potrà reinventare la natura e noi stessi, in quella che può essere definita una seconda genesi – ma perché è il primo che, oltre a essere distribuito su carta e in digitale, è stato stampato usando come supporto la regina delle molecole biologiche, il DNA. Church ha fatto del libro 70 miliardi di copie nel proprio laboratorio e per contenerle gli è bastata una minuscola provetta. L’exploit, annunciato il 16 agosto dalla rivista Science, dimostra che il DNA ha potenzialità straordinarie per l’immagazzinamento dei dati digitali e conferma la vena eccentrica di questo scienziato a cui piace lavorare al confine tra biologia e informatica, tra possibile e impossibile.

Church nasce nel 1954 in Florida e a 10 anni è già in grado di costruire dei calcolatori rudimentali ma funzionanti, utilizzando pezzi di apparecchi radiofonici. A 16 anni si scrive da solo i software, spaziando dalla modellizzazione ecologica alla poesia algoritmica.

A 22 rischia di essere cacciato dalla Duke University, perché è così assorbito dalla ricerca biochimica da disertare le lezioni. Per fortuna c’è Harvard pronta ad accoglierlo, sotto la guida di Walter Gilbert. Insieme al futuro premio Nobel per la chimica, il giovane Church mette a punto uno dei primi metodi per studiare le sequenze di DNA. Sono sue le intuizioni che oggi fanno funzionare le macchine sequenziatrici di ultima generazione ed è questo il campo in cui tuttora lavora. Sviluppa idee innovative per leggere, scrivere, modificare il DNA in modo sempre più economico e preciso, per cambiarne il codice, persino, e traghettare l’ingegneria genetica in una fase nuova, di piena maturità e grandi ambizioni.

Church immagina di capovolgere l’orientamento delle molecole che costituiscono il micromondo naturale, come in un gioco di specchi che aprirebbe la strada a chissà quali applicazioni.

Imponente e suggestivo anche nel fisico – è un vegano alto quasi due metri, con la barba grigia come i saggi e i maghi – contrappone alla cultura della privacy quella della trasparenza. Il suo genoma è pubblicamente accessibile e migliaia di volontari hanno deciso di seguirne l’esempio, prendendo parte al suo Personal Genome Project.

Church non è stato il primo a usare il DNA per scrivere, ma gli altri pionieri si sono accontentati di inserire semplici frasi, mai libri interi. Avrebbe voluto riservare quest’onore a Moby Dick di Herman Melville, ma poi ha scelto Regenesis, per dimostrare che il sistema funziona perfettamente anche per le immagini. Il testo, lungo 53.000 parole e corredato da 11 immagini, è stato prima tradotto nella sfilza di 0 e di 1 del codice binario, quindi in una successione di A, T, G e C (le ‘lettere’ del DNA), con un tasso minimo di errori: appena due per milione di bit.

In quest’ottica la scrittura consiste nella sintesi del DNA, la lettura nel suo sequenziamento. Per codificare e poi decodificare tutto, insieme a Yuan Gao e Sriram Kosuri, Church ha impiegato due settimane, ed è questo il motivo per cui le provette non sostituiranno i volumi di carta nelle librerie di casa per molto tempo ancora. Il DNA però offre altri vantaggi. Al di fuori delle cellule viventi, si conserva in modo stabile per secoli, anzi millenni. Ma soprattutto può immagazzinare dati a una densità che è circa un milione di volte maggiore di quella di un hard disc, surclassando le tecnologie sperimentali più avanzate come l’olografia quantistica. Quattro grammi di DNA potrebbero contenere i dati digitali che l’umanità crea in un anno. Un supporto grande come un dito basterebbe a immagazzinare Internet. Come useremo tutto questo spazio? Largo all’immaginazione.

George Church nel suo Regenesis (scritto con il giornalista Red Egis, già autore di Great Mambo Chicken and the Transhuman Conditionintravede, nel prossimo futuro, il seguente scenario: a) il tuo genoma è sequenziato; b) una serie di cellule staminali pluripotenti sono create in laboratorio da tuoi tessuti; c) quanto necessario potrai riparare organi e tessuti danneggiati dal passare del tempo; d) i più avventurosi (previdenti?) potenzieranno il proprio genoma con, per esempio, geni tipicamente riscontrati fra i supercentenari. Come reagirà il grande pubblico di fronte a scenari simili? Church si aspetta che i primi a sfruttare le terapie rigenerative avranno bisogno di non poco coraggio. Probabilmente si tratterà di persone seriamente malate le quali saranno non solo curate, ma si sentiranno anche molto meglio, dopo la terapia, di quanto si sentissero prima di sviluppare la malattia in questione. Nel curare una specifica malattia, i pazienti saranno anche ringiovaniti. A quel punto la voce si diffonderà molto in fretta...

Letture: Regenesis, di George M. Church. Come la biologia sintetica re-inventera' la Natura e noi stessi 28 novembre 2012

Qualche giorno fa ha fatto il giro del mondo la notizia di un ragazzo di 18 anni della provincia di Torino affetto da un tumore alle ossa e salvato grazie a un emibacino artificiale. Oltre dieci ore di intervento hanno permesso di sostituire la parte destra del bacino e l’anca affetta da osteosarcoma, con una protesi di titanio con rivestimento in  tantalio (un materiale che si integra con le ossa umane) realizzato negli Stati Uniti, in base al calco ricavato dalla Tac del paziente. Sempre presso la stessa struttura, l'ospedale Infantile Regina Margherita della Città della Salute di Torino, qualche mese fa a un bambino di quattro anni, affetto da una grave insufficienza renale, era stata impiantata un’arteria artificiale, per permettere il passaggio del sangue al cuore. I grossi cateteri per la dialisi avevano infatti occluso i vasi centrali che portano al cuore.

In entrambi i casi un “pezzo di ricambio” artificiale e costruito ad hoc, ha permesso di salvare la vita a questi giovani pazienti. Certo il caso del bambino di quattro anni non rappresenta una novità se si pensa che gli stent (strutture cilindriche di metallo utilizzate negli organi cavi, come i vasi o l’intestino, per mantenere aperti i passaggi occlusi) da anni vengono usati in chirurgia per ridurre una stenosi o evitare un aneurisma; o se si pensa ai pacemaker, dispositivi elettrici in grado di stimolare elettricamente il battito del cuore quando questo non avviene più spontaneamente; alle protesi d’anca, per cui l'articolazione di un'anca malata viene sostituita con un impianto artificiale fatto di metallo, ceramica o plastica; o banalmente anche agli impianti acustici per la perdita dell’udito e agli occhiali, che certo non sono impiantati all’interno del nostro corpo, ma sono pur sempre estensioni artificiali del nostro organismo che ci permettono di migliorare la nostra salute.

In questo senso siamo tutti già dei cyborg. Organismi costituiti da una parte umana-biologica (ancora preponderante, per il momento) e una artificiale che utilizziamo per migliorare la nostra performance. Ma c’è anche chi, superata la moda di piercing e tatuaggi, per avvicinarsi di più a un organismo cibernetico, si fa impiantare un magnete sottopelle. Un microchip posizionato nel dito (dove le terminazioni nervose sono maggiori), generalmente anulare, in grado di far sentire i campi magnetici presenti nelle vicinanze e sollevare piccoli oggetti metallici, come graffette o spilli. O un radio-frequency identification (RFID) chip, impiantato nello spazio tra il pollice e il dito indice, che dovrebbe permettere in pratica un’autenticazione più veloce, economica e affidabile, rispetto altri dati biometrici, come le impronte digitali o scansioni facciali, come riporta Forbes. «Quando il chip viene colpito con un segnale a radiofrequenza, emette un numero identificativo unico che funziona come una lunga password, difficili da indovinare. Chi ha l’impianto, con un semplice gesto della mano può recuperare le chiavi dalla tasca, aprire le automobili, accendere o spegnere i computer, lo smartphone e anche la luce di casa».

Tutto perfettamente in linea con la  filosofia del transumanesimo (h+). 

Il cuore del biohacking è senza dubbio il Regno Unito dove si trovano due delle figure di spicco del movimento: Lepht Anonym, una giovane donna di Aberdeen che senza alcuna prudenza si è impiantata da sola protesi metalliche e macchine, e Kevin Warwick, un professore dell'Università di Reading del dipartimento di cibernetica, che per eseguire i suoi impianti si appoggia a uno staff qualificato di tecnici medici. Già nel 1998 Warwick si fece impiantare un RFID chip – e fu uno dei primi a farlo – e nel 2002, dei sensori cibernetici nei nervi del braccio. «Il suo braccio è pieno di macchine complesse – racconta Ben Popper su The Verge – che permettono a Warwick di manipolare una mano robotica a distanza, uno sorta di specchio del suo braccio in carne e ossa. Non solo, ma l’impulso può andare in entrambe e direzioni. La moglie di Warwick, Irena, ha invece impiantato un sistema cibernetico semplice. Quando qualcuno le stringe la mano, Warwick anche oltre oceano era in grado di provare la stessa sensazione alla mano. È una sorta di telepatia cibernetica, come ha scritto Warwick, o empatia, per cui i suoi nervi sono stati modificati per sentire quello che sente lei, attraverso una serie di bit di dati che viaggiano su Internet».

Nel 2012 il lavoro di Warwick venne salutato come un importante passo in avanti per aiutare le persone prive di arti o paralizzate, per riconquistare una serie di capacità. «Sono contento se questa scoperta porterà a nuove e potenziali terapie mediche – aveva affermato il professore – ma quello che veramente mi interessa è il potenziamento delle capacità umane a un livello superiore. Dieci anni fa questo avrebbe sconvolto molte persone: a meno che l’obiettivo finale non fosse aiutare i disabili, le persone non erano pronti ad accettarla».

A fine febbraio del 2015 le agenzie riportano la notizia di una nuova ricerca, una delle tante, che ha permesso di impiantare  una mano bionica mossa dal pensiero su tre pazienti, che avevano subito delle lesioni del plesso brachiale. Chissà se, come ha predetto il miliardario russo Dmitry Itskov, nel 2045 con poche e semplici mosse diventeremo davvero immortali. 

Cyborg e post umani, ecco la nuova evoluzione Cristina Tognaccini 8/03/2015

Il movimento Do-It-Yourself Biology rivendica una continuità ideale con il mondo hacker: se a partire dagli anni ’70 le più grandi rivoluzioni dell’informatica sono nate “in garage”, la speranza è che anche per le biotecnologie le grandi rivoluzioni nascano da menti creative fuori dagli schemi accademici, che si scambino informazioni in un’ottica open source.



Anno di Ford 632, corrispondente all'anno 2540 della nostra era. A seguito di una devastante guerra di nove anni (iniziata negli anni quaranta), l'intero pianeta viene riunito in un unico Stato, governato da dieci "Coordinatori Mondiali".
La nuova società è basata sui principi della produzione in serie, applicati inizialmente nelle industrie automobilistiche di Ford alla produzione del "Modello T". Per questo Ford è il Dio di questa nuova società ed il segno della "T" ha rimpiazzato il segno della croce cristiana. La produzione in serie viene applicata anche alla riproduzione umana, resa completamente extrauterina. Gli embrioni umani vengono prodotti e fatti sviluppare in apposite fabbriche secondo quote prestabilite e pianificate dai coordinatori mondiali.
Per impedire nascite naturali, e quindi non controllate, vengono usate apposite pratiche di contraccezione, insegnate ai giovani nelle scuole; neanche più il cognome indica l'appartenenza a una famiglia, dato che ogni individuo può scegliere il nome e il cognome che preferisce.
Gli esseri umani in questa società sono divisi in caste, create tramite un ritardo controllato dello sviluppo degli embrioni ottenuto tramite privazione dell'ossigeno, in modo da influenzarne il futuro sviluppo fisico e intellettivo. Le tre caste inferiori sono formate da gruppi di gemelli identici, ottenute indebolendo gli embrioni fino a farli frammentare.
La casta alfa consiste degli individui destinati al comando, i beta coprono incarichi amministrativi che richiedono un'istruzione superiore, ma senza le responsabilità del comando. Le tre caste inferiori sono le gammadelta e epsilon in grado decrescente di intelligenza. Gli epsilon sono creati e addestrati per occuparsi dei lavori più umili e nelle condizioni più dure senza lamentarsene. In genere, tutti gli individui sono sottoposti a condizionamento mentale per conformarsi al ruolo che ricopriranno nella società.
Come "rimedio" per ogni eventuale infelicità, alla popolazione viene fornito un medicinale chiamato soma, in realtà una droga euforizzante e antidepressiva, garantendo così un ulteriore controllo della popolazione.
L'umanità è finalmente libera da preoccupazioni, sana, tecnologicamente avanzata, priva di povertà e guerra, permanentemente felice.

Il mondo nuovo da Wikipedia

Non siamo, ahimè, molto lontani dallo scenario distopico descritto da una miriade di opere letterarie, cinematografiche e televisive. 

Dal mitico "X Files", passando per "L'Ombra dello Scorpione" di Stephen King, alla serie candese "ReGenesis", dove un’organizzazione chiamata NorBAC (North American Biotechnology Advisory Commission) indaga su i mostri creati dalla biotecnologiaarmi biologiche, organismi geneticamente modificati, embrioni clonati, virus killer. 

In "Leviathanun film di fantascienza del 1989, diretto da George Pan Cosmatos, un'esperimento genetico trasforma l'equipaggio di un sottomarino in creature mostruose.

In "Hitman Agent 47", tratto da una famosa serie di videogame, un assassino geneticamente modificato cerca di scombinare i piani di una multinazionale che vuole sfruttare il segreto della sua creazione per assemblare un esercito di spietati e letali super-assassini.
Nella serie "Resident Evil", sempre tratta da un videogioco,  la multinazionale Umbrella Corporation causa un'epidemia batteriologica che trasforma la popolazione in orrendi mostri zombie. 
In Godsend - Il male è rinato (Godsend) un film del 2004 diretto da Nick Hamm, con Robert De Niro un bambino clonato ha delle allucinazioni e diventa maligno. 

Nel film “Gattaca, la porta dell'universo”, la pratica delle diagnosi pre-impianto per selezionare il corredo genetico dei nascituri in vitro ha dato origine alla sottoclasse dei “non-validi” (le persone nate in modo naturale, geneticamente imperfette).

In “The Island” (Michael Bay, USA, 2005), Lincoln Six-Echo (Ewan McGregor), un clone creato in segreto e fatto vivere in un ambiente totalmente virtuale, sta per essere soppresso (mandato sull'Isola) per ricavare organi, tessuti o prole, che saranno poi ceduti a facoltosi clienti disposti a pagare cifre astronomiche pur di non invecchiare o soffrire.

Il profetico romanzo breve "Gli Occhi di Heisenberg" di Frank Herbert, tratta il tema dell'ingegneria genetica legata al tema dell'immortalità. Il mondo è dominato dal regime totalitario degli Optimati, individui potenziati geneticamente ed immortali che soggiogano il resto dell'umanità, cui non è nemmeno concesso il diritto di procreare se sprovvisti di alcune peculiari caratteristiche genetiche.

Nei tre volumi che compongono la trilogia “Xenogenesis”, della scrittrice afroamericana Octavia Butler, la trasformazione dell'umanità è ottenuta mediante biotecnologia aliena, fornita da ingegneri genetici chiamati “ooloi”, intenti a far accoppiare gli umani con la specie aliena degli Oankali.

Tutto comincia con "Frankenstein o il Prometeo Moderno", di Mary Shelley (1818) 

... fu partorito da un sogno. O meglio, da un incubo. La Shelley vide chiaramente il delirio di onnipotenza dell’uomo che si vuole fare simile a Dio, con la capacità di decidere della vita e della morte. Il risultato è una mostruosità della tecnica, una "creatura" che è un insieme di organi umani e animali assemblati, una "natura morta", incarnazione della paura che all'epoca accompagnava le nuove scoperte tecno-scientifiche, come ad es. l'elettricità, e la comparsa delle macchine, che apparivano come mostruose. Già allora si parlava di riportare in vita i morti.

La creatura si dimostra dapprima ingenua, di indole mite, perfino desiderosa di amore fisico, di affetto e simpatia, ma per il suo aspetto abominevole è rifiutata da tutti. Respinta dagli uomini, diviene conscia della propria deformità e, colta da una furia omicida, sfugge ad ogni controllo e si rivolta contro il suo creatore.

Il vero protagonista del mito è il Dr. Frankenstein, il Prometeo Moderno, che si specchia nella sua creatura. Non a caso, l'autrice è una donna, che aveva intuito i pericoli che stava correndo la natura (femminile) rispetto all'invasione della cultura (maschile).

La natura è descritta da Shelley come una femmina passiva stuprata allo scopo di soddisfare i desideri dello scienziato maschio.

"Lo scienziato che analizza, manipola e tenta di controllare la natura, inconsciamente pratica una forma di politica sessuale oppressiva. Interpretando la natura come l'Altro femminile, egli tenta di far servire ai propri fini la natura, per gratificare i suoi desideri di potere" (Ann Mellor, "Mary Shelley Her Life, her Fiction, her Monsters", Methuen, 1988).

Richard Lynn, professore all'Università dell'Uster, per giustificare la selezione degli embrioni spiega che: “il  progresso evoluzionistico significa l'estinzione dei meno competenti”. I transumanisti sono stati i primi fautori della clonazione riproduttiva e dell'utilizzo di farmaci come Ritalin (una anfetamina che adesso somministrano anche ai neonati, per farli stare buoni, ndr), Viagra e Prozac, la “soma” di Aldous Huxley.

Il loro slogan recita: “Perché non usare gli strumenti della genetica per renderci più veloci, più sani e più longevi?”. Vorrebbero embrioni geneticamente modificati per produrre “figli forti e attraenti”. Se il vitro fallisce, auspicano una “Kristallnacht” delle provette e un nuovo eterno inizio. Non a caso, considerano loro capostipite il filosofo inglese William Godwin, che nel 1793 voleva ricorrere all'eugenetica per “estirpare tutte le infermità della natura”, compresa la malinconia.


La scienza può curare, salvare vite, ma anche essere asservita al male.

Aborti selettivi, distruzione di embrioni umani, manipolazioni geneticheeutanasia ribattezzata come "dolce morte": tutti attacchi alla dignità umana in nome del mito dell’efficienza e della perfezione... Quanto è viva a 70 anni di distanza la tentazione eugenetica?

È paradossale che la medicina, che dovrebbe avere come obiettivo primario la salute, in questo caso si è fatta promotrice, sia sulle basi teoriche che poi anche nella pratica, degli eccidi e degli orrori dello sterminio. È una considerazione molto importante che serve soprattutto come lettura dell’attualità. 

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