Viral and Host Mediators of Non-Suppressible HIV-1 Viremia

Author:

Mohammadi AbbasORCID,Etemad Behzad,Zhang Xin,Li Yijia,Bedwell Gregory J.,Sharaf Radwa,Kittilson Autumn,Melberg Meghan,Wong Colline,Fajnzylber Jesse,Worrall Daniel P.,Rosenthal Alex,Jordan Hannah,Jilg Nikolaus,Kaseke Clarety,Giguel Francoise,Lian Xiaodong,Deo Rinki,Gillespie Elisabeth,Chishti Rida,Abrha Sara,Adams Taylor,Siagian Abigail,Anderson Peter L.,Deeks Steven G.ORCID,Lederman Michael M.,Yawetz Sigal,Kuritzkes Daniel R.,Lichterfeld Mathias D.,Tsibris Athe,Carrington Mary,Brumme Zabrina L.,Castillo-Mancilla Jose R.,Engelman Alan N.,Gaiha Gaurav D.,Li Jonathan Z.

Abstract

AbstractNon-suppressible HIV-1 viremia (NSV) can occur in persons with HIV despite adherence to combination antiretroviral therapy (ART) and in the absence of significant drug resistance. Here, we show that plasma NSV sequences are comprised primarily of large clones without evidence of viral evolution over time. We defined proviruses that contribute to plasma viremia as “producer”, and those that did not as “non-producer”. Compared to ART-suppressed individuals, NSV participants had a significantly larger producer reservoir. Producer proviruses were enriched in chromosome 19 and in proximity to the activating H3K36me3 epigenetic mark. CD4+cells from NSV participants demonstrated upregulation of anti-apoptotic genes and downregulation of pro-apoptotic and type I/II interferon-related pathways. Furthermore, NSV participants showed no elevation in HIV-specific CD8+cell responses and producer proviruses were enriched for HLA escape mutations. We identified critical host and viral mediators of NSV that represent potential targets to disrupt HIV persistence and promote viral silencing.

Publisher

Cold Spring Harbor Laboratory

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