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.
| Original language | English (US) |
|---|---|
| Pages (from-to) | 2167-2175 |
| Number of pages | 9 |
| Journal | Journal of Infectious Diseases |
| Volume | 225 |
| Issue number | 12 |
| DOIs | |
| State | Published - Jun 15 2022 |
Bibliographical note
Publisher Copyright:© 2022 The Author(s) 2022. Published by Oxford University Press for the Infectious Diseases Society of America.
UN SDGs
This output contributes to the following UN Sustainable Development Goals (SDGs)
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SDG 3 Good Health and Well-being
Keywords
- HIV reservoir
- acute HIV infection
- antiretroviral therapy
- in situ hybridization
- lymphoid tissues
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