Author:
Abrahams Melissa-Rose,Joseph Sarah B.,Garrett Nigel,Tyers Lynn,Moeser Matthew,Archin Nancie,Council Olivia D.,Matten David,Zhou Shuntai,Doolabh Deelan,Anthony Colin,Goonetilleke Nilu,Karim Salim Abdool,Margolis David M.,Pond Sergei Kosakovsky,Williamson Carolyn,Swanstrom Ronald
Abstract
AbstractAlthough antiretroviral therapy (ART) is highly effective at suppressing HIV-1 replication, the virus persists as a latent reservoir in resting CD4+ T cells during therapy. Little is known about the dynamics of reservoir formation and this reservoir forms even when ART is initiated early after infection. The reservoir of individuals who initiate therapy in chronic infection is generally larger and genetically more diverse than that of individuals who initiate in acute infection, suggesting the reservoir is formed continuously throughout untreated infection. To determine when viruses enter the latent reservoir, we compared sequences of replication-competent viruses from resting CD4+ T cells from nine women on therapy to viral sequences circulating in blood collected longitudinally prior to therapy. We found that 78% of viruses from the latent reservoir were most genetically similar to viruses replicating just prior to therapy initiation. This proportion is far greater than expected if the reservoir forms continuously and is always long-lived. Thus, therapy alters the host environment in a way that allows the formation of a majority of the long-lived latent HIV-1 reservoir.One Sentence SummaryMost of the long-lived, replication-competent HIV-1 reservoir is formed at the time of therapy initiation.
Publisher
Cold Spring Harbor Laboratory
Cited by
2 articles.
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