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Disease · Infectious disease

HIV

A virus that hides inside the genome of the cells it infects — which is why editing has been proposed both to block entry and to cut the virus out.

Phase I CCR5virusexcision
Clinical research Being tested in people in registered clinical trials. Being in trials is not evidence that a treatment works or is safe.

简单说明

HIV infects immune cells and then writes its own genes into their DNA, where drugs cannot reach it. Daily medication keeps the virus suppressed, but stop the medication and the hidden copies wake up. Two editing ideas follow from that. The first removes the doorway the virus uses to get into cells — a gene called CCR5, which some people are naturally born without and who are largely resistant to infection. The second tries to cut the viral DNA out of the genome directly.

深入了解

HIV integrates as a provirus into host cell DNA, establishing a latent reservoir that antiretroviral therapy suppresses but does not eliminate. Editing strategies target CCR5, the principal co-receptor for R5-tropic HIV — homozygous CCR5-Δ32 individuals are largely resistant, and allogeneic transplant from CCR5-Δ32 donors has produced sustained remission in a small number of patients — or attempt excision of integrated provirus. Sangamo's zinc-finger CCR5 disruption programme was the first human gene-editing trial of any kind.

Why the natural experiment matters

About one per cent of people of northern European ancestry carry two copies of CCR5-Δ32, a deletion that removes the receptor, and they are largely resistant to the common form of HIV while appearing otherwise healthy. A small number of patients — beginning with Timothy Ray Brown, the 'Berlin patient' — have achieved long-term remission after receiving bone marrow transplants from CCR5-Δ32 donors for unrelated cancers. That is proof the biology works. The problem is that a marrow transplant is a dangerous procedure that no one would undergo for HIV alone, given how well antiretroviral therapy works.

Honest status

Editing approaches to HIV remain early-phase and have not produced durable control off medication in trials. The comparator is genuinely excellent: modern antiretroviral therapy gives near-normal life expectancy. Any editing approach has to beat that on convenience or on cure, and neither has been shown.

ImportantThis is also the area of the field's worst episode: in 2018 He Jiankui edited CCR5 in human embryos and brought about the birth of edited children, an act condemned worldwide and for which he was imprisoned. That was germline editing of healthy embryos, and it is unrelated to the legitimate somatic research described here.
Honest status
Virus particles at the surface of an immune cell, at the receptor they use to enter. Illustration generated for The CRISPR Atlas — a visual aid, not a photograph or a literal depiction of molecular structure.

Sources

Connected in the Atlas

Every entry on this site is linked to the others it relates to. These connections are part of the record, not a search result.

仅供教育参考 本页面为参考资源,不构成医疗建议。研究进展和监管状态会发生变化;请查看上方的最后更新日期,并对重要信息进行核实,以所列主要来源为准。