Viral and host mediators of non-suppressible HIV-1 viremia.
СтатьяНазвание и аннотация: Перевод в очереди
Обработка статьи · этапы, ошибки и управление
Загрузка состояния…
Ошибки и ограничения
История · было → стало
Состояние обновляется каждые 5 секунд, пока блок открыт. Процент показывается только там, где известен объём работы. Пауза останавливает продолжение этапа; текущий запрос к источнику может завершиться.
Mohammadi Abbas, Etemad Behzad, Zhang Xin, Li Yijia, Bedwell Gregory J, Sharaf Radwa, Kittilson Autumn, Melberg Meghan, Crain Charles R, Traunbauer Anna K, 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, Dorazio Dominic, Anderson Peter L, Deeks Steven G, Lederman Michael M, Yawetz Sigal, Kuritzkes Daniel R, Lichterfeld Mathias D, Sieg Scott, Tsibris Athe, Carrington Mary, Brumme Zabrina L, Castillo-Mancilla Jose R, Engelman Alan N, Gaiha Gaurav D, Li Jonathan Z
Аннотация
Non-suppressible HIV-1 viremia (NSV) is defined as persistent low-level viremia on antiretroviral therapy (ART) without evidence of ART non-adherence or significant drug resistance. Unraveling the mechanisms behind NSV would broaden our understanding of HIV-1 persistence. Here we analyzed plasma virus sequences in eight ART-treated individuals with NSV (88% male) and show that they are composed of large clones without evidence of viral evolution over time in those with longitudinal samples. We defined proviruses that match plasma HIV-1 RNA sequences as 'producer proviruses', and those that did not as 'non-producer proviruses'. Non-suppressible viremia arose from expanded clones of producer proviruses that were significantly larger than the genome-intact proviral reservoir of ART-suppressed individuals. Integration sites of producer proviruses were enriched in proximity to the activating H3K36me3 epigenetic mark. CD4+ T cells from participants with NSV demonstrated upregulation of anti-apoptotic genes and downregulation of pro-apoptotic and type I/II interferon-related pathways. Furthermore, participants with NSV showed significantly lower HIV-specific CD8+ T cell responses compared with untreated viremic controllers with similar viral loads. We identified potential critical host and viral mediators of NSV that may represent targets to disrupt HIV-1 persistence.