Paradoxically greater persistence of HIV RNA-positive cells in lymphoid tissue when ART is initiated in the earliest stage of infection

E Kroon, S Chottanapund… - The Journal of …, 2022 - academic.oup.com
E Kroon, S Chottanapund, S Buranapraditkun, C Sacdalan, DJ Colby, N Chomchey…
The Journal of Infectious Diseases, 2022academic.oup.com
Starting antiretroviral therapy (ART) in Fiebig 1 acute HIV infection limits the size of viral
reservoirs in lymphoid tissues, but does not impact time to virus rebound during a treatment
interruption. To better understand why the reduced reservoir size did not increase the time to
rebound we measured the frequency and location of HIV RNA+ cells in lymph nodes from
participants in the RV254 acute infection cohort. HIV RNA+ cells were detected more
frequently and in greater numbers when ART was initiated in Fiebig 1 compared to later …
Abstract
Starting antiretroviral therapy (ART) in Fiebig 1 acute HIV infection limits the size of viral reservoirs in lymphoid tissues, but does not impact time to virus rebound during a treatment interruption. To better understand why the reduced reservoir size did not increase the time to rebound we measured the frequency and location of HIV RNA+ cells in lymph nodes from participants in the RV254 acute infection cohort. HIV RNA+ cells were detected more frequently and in greater numbers when ART was initiated in Fiebig 1 compared to later Fiebig stages and were localized to the T-cell zone compared to the B-cell follicle with treatment in later Fiebig stages. Variability of virus production in people treated during acute infection suggests that the balance between virus-producing cells and the immune response to clear infected cells rapidly evolves during the earliest stages of infection.
Clinical Trials Registration: NCT02919306.
Oxford University Press