Emerging microbes & infections · 2024
Effective and targeted latency reversal in CD4+ T cells from individuals on long term combined antiretroviral therapy initiated during chronic HIV-1 infection.
СтатьяНазвание и аннотация: Перевод пока не подготовлен
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Ngo Minh Ha, Pankrac Joshua, Ho Ryan C Y, Ndashimye Emmanuel, Pawa Rahul, Ceccacci Renata, Biru Tsigereda, Olabode Abayomi S, Klein Katja, Li Yue, Kovacs Colin, Assad Robert, Jacobson Jeffrey M, Canaday David H, Tomusange Stephen, Jamiru Samiri, Anok Aggrey, Kityamuweesi Taddeo, Buule Paul, Galiwango Ronald M, Reynolds Steven J, Quinn Thomas C, Redd Andrew D, Prodger Jessica L, Mann Jamie F S, Arts Eric J
Аннотация
To date, an affordable, effective treatment for an HIV-1 cure remains only a concept with most "latency reversal" agents (LRAs) lacking specificity for the latent HIV-1 reservoir and failing in early clinical trials. We assessed HIV-1 latency reversal using a multivalent HIV-1-derived virus-like particle (HLP) to treat samples from 32 people living with HIV-1 (PLWH) in Uganda, US and Canada who initiated combined antiretroviral therapy (cART) during chronic infection. Even after 5-20 years on stable cART, HLP could target CD4+ T cells harbouring latent HIV-1 reservoir resulting in 100-fold more HIV-1 release into culture supernatant than by common recall antigens, and 1000-fold more than by chemotherapeutic LRAs. HLP induced release of a divergent and replication-competent HIV-1 population from PLWH on cART. These findings suggest HLP provides a targeted approach to reactivate the majority of latent HIV-1 proviruses among individuals infected with HIV-1.