Russian CRISPR-baby scientist has started editing genes in eggs from a deaf woman –

Denis Rebrikov, Russian biochemist.

Denis Rebrikov, Russian biochemist.

Denis Rebrikov plans to soon publish his experiments to repair genes in human eggs.Credit: Andrey Rudakov/Bloomberg/Getty

Russian biologist Denis Rebrikov has started gene editing eggs donated by a woman who was born deaf to learn how to allow her to give birth to children without the genetic mutation that impairs her hearing. The news, detailed in an e-mail he sent Nature on 17 October, is the latest in a saga that kicked off this past June when Rebrikov told Nature of his controversial intention to create gene-edited babies resistant to HIV using the popular CRISPR tool.

Rebrikov’s latest e-mail (see Box) follows a September report in Russian magazine N+1 that one deaf couple had started procedures to procure eggs that would be used to create a gene-edited baby — and it is the first time Rebrikov has claimed to have actually obtained, and edited, such eggs.

In his e-mail to Nature, Rebrikov makes clear that he does not plan to create such a baby yet — and that his previously reported plan to apply this month for permission to implant gene-edited embryos in women has been pushed back.

Instead, he says that he will soon publish the results of his egg experiments, which involved testing CRISPR’s ability to repair a gene linked to deafness, called GJB2, in eggs and bodily cells taken from people with this mutation. People with two mutated copies of GJB2 cannot hear well without interventions, such as hearing aids or cochlear implants. Rebrikov says these results will lay the groundwork for the clinical work.

Rebrikov adds that he has permission from a local review board to do such research, but that this does not allow transfer of gene-edited eggs into the womb and subsequent pregnancy.

He is in discussion with four other couples in which both would-be parents have two mutated GJB2 genes, he says. Rebrikov says he wants to help couples such as these to have a child with unimpaired hearing.

Rebrikov also provided further information about the egg donor and her plans in his most recent e-mail. In September, N+1 had reported that the couple didn’t sign a consent form and had backed away from the idea of creating a gene-edited child, citing personal reasons.

But Rebrikov now says that this is only a temporary hurdle. He notes that the woman who donated the eggs has taken a one-month ‘pause’ while she gets a cochlear implant.

Rebrikov also emphasized that he will not move forward without approval from the Ministry of Health of the Russian Federation. “I will definitely not transfer an edited embryo without the permission of the regulator.”

That might not come soon. Last week, the ministry released a statement saying that production of gene-edited babies is premature. Rebrikov says “it is hard to predict” when he will get permission, but it will be after all the necessary safety checks.

Doubling down

Rebrikov shot to fame in June with the news of his plans to make HIV-resistant babies. The news shocked international researchers, who feared that he was following in the footsteps of Chinese scientist He Jiankui, who announced the controversial birth of the world’s first babies, twin girls, with edited genomes last year.

Rebrikov plans to use CRISPR to disrupt the same gene that He did — CCR5. The protein made by the CCR5 gene allows HIV to enter cells, and people with a mutated copy of this gene are far less likely to get the disease. But many scientists say that the benefits — possible resistance to HIV — are not worth the unknown risks of gene editing, because there are other ways to prevent passing HIV from parent to child.

According to Rebrikov’s latest email, he has not abandoned plans to edit the CCR5 gene. He says he started looking for women with HIV who wanted to have a baby and who have responded poorly to HIV drugs. He argues that such people might be good candidates for the procedure because they have an elevated chance of passing the virus to their children, though many scientists think any attempt to use gene editing in embryos to modify CCR5 is misguided. He told Nature he is still looking for such women. “But there are very few of them,” he says.

In the meantime, Rebrikov has taken on another project — repairing the GJB2 gene in human embryos.

Some scientists and ethicists also call into question the benefits of this procedure because hearing loss is not a fatal condition. “The project is recklessly opportunistic, clearly unethical, and damages the credibility of a technology that is intended to help, not harm,” says Jennifer Doudna, a pioneer of the CRISPR gene-editing tool and a biologist at the University of California, Berkeley.

In the wake of He’s explosive revelation in November 2017, the World Health Organization tasked a committee with developing an international framework to govern the clinical use of gene editing. In August, the WHO committee also launched an international registry of clinical research using gene editing in humans to oversee this practice. An international commission created by the US National Academy of Sciences, US National Academy of Medicine and the Royal Society of the United Kingdom is also preparing a framework to guide clinical research in germline gene editing, which is expected to be released in spring 2020. The commission will hold a public meeting on November 14 and 15 to gather ideas for it.

He Jiankui And His Genetic Research Team.

He Jiankui And His Genetic Research Team.

He Jiankai claims he created the world’s first babies with edited genomes.Credit: Visual China Group/Getty

Rebrikov told Bloomberg last month that he wants to follow regulations that have been internationally agreed on when moving gene editing to the clinic. But he also expressed frustration that none exist yet.

Robin Lovell-Badge, a developmental biologist at the Francis Crick Institute in London and a member of the WHO committee, says that Rebrikov should wait until a clear framework has been agreed on, and that this will take time. “This is not a simple matter, and it is ridiculous to think that we can come up with global solutions to regulation in a very complex scientific and potentially clinical area in a few months.”

Nature’s questions and Rebrikov’s responses

Below are edited versions of the questions that Nature sent to Rebrikov, and his answers.

Some scientists and bioethicists say that deafness is not a life-threatening condition and therefore should not be the target of a risky treatment like this.

Any new drug carries certain risks. The deafness model is the most appropriate for applying genomic editing at the zygote [newly fertilized egg] stage. And it is only for deaf parents to decide whether … deafness is enough to not expect the same for their child.

In particular, scientists worry about off-target mutations — which are potentially dangerous and could be introduced away from the intended edit.

Of course we worried about those. We have a long and reasonable algorithm for checking off-target activity. I’d like to discuss the algorithm for checking the efficiency and safety of the technology, rather than the prematureness of the method.

Some also warn that because the CRISPR repair mechanism is inefficient, there is a high likelihood of producing children with mosaicism — a mix of edited and unedited cells. Are you worried about this?

Yes. Unfortunately, due to the impossibility of a complete analysis of the embryo (we only look at a biopsy of 5–7 cells), we will never be completely sure of the absence of mosaicism in transferred embryos. But statistically (in experiments), it is possible to show the permissible percentage of mosaicism or its absence.

A health-ministry press release says that a 2012 decree on artificial reproductive technologies does not allow genetically modified embryos to be implanted. Does this change your plans?

Laws are written to change them. As soon as we demonstrate the safety of technology, the rule will change.

He Jiankui worked mostly in secrecy before announcing his gene-edited babies. You appear to work hard to maintain channels of communication with scientists and regulators.

I have no problems in communication with researchers and regulators concerning my research. But both (researchers and regulators) want to look at the correct demonstration of safety and efficiency. And I agree with that.

One argument against your plans is that the focus of gene editing should be on adult cells to cure disease, rather than on embryos. They worry embryo editing will be a distraction.

Agree. To date, the somatic-cell technologies have had much more impact. But I don’t think that zygote [newly fertilized egg] genome editing will negatively affect the correction of somatic mutations.

Those working on international frameworks to guide the clinical application of human-embryo editing have suggested that, until they are done, clinical research with edited embryos should slow down.

Are you serious? Where did you see the researcher willing to slow down?

The Russian health ministry issued a statement last week saying that it follows the position of the World Health Organization committee: it is too soon to do such experiments. Will you try to apply anyway?

What does it mean, too soon? Lenin said “yesterday was too early, tomorrow it will be too late”.

The interview has been edited for length and clarity.

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