Distinct gene expression by expanded clones of quiescent memory CD4+ T cells harboring intact latent HIV-1 proviruses

被引:24
作者
Weymar, Georg H. J. [1 ]
Bar -On, Yotam [2 ]
Oliveira, Thiago Y. [1 ]
Gaebler, Christian [1 ]
Ramos, Victor [1 ]
Hartweger, Harald [1 ]
Breton, Gaelle [1 ]
Caskey, Marina [1 ]
Cohn, Lillian B. [3 ]
Jankovic, Mila [1 ]
Nussenzweig, Michel C. [1 ,4 ]
机构
[1] Rockefeller Univ, Lab Mol Immunol, New York, NY 10065 USA
[2] Technion Israel Inst Technol, IL-320003 Haifa, Israel
[3] Fred Hutchinson Canc Res Ctr, Vaccine & Infect Dis Div, Seattle, WA 98109 USA
[4] Howard Hughes Med Inst, Chevy Chase, MD 20815 USA
基金
美国国家卫生研究院;
关键词
RESERVOIR IMPLICATIONS; PERSISTENCE; IDENTIFICATION; LYMPHOCYTES; PHENOTYPE; HETEROGENEITY; PROLIFERATION; ESTABLISHMENT; REACTIVATION; RESPONSES;
D O I
10.1016/j.celrep.2022.111311
中图分类号
Q2 [细胞生物学];
学科分类号
071009 ; 090102 ;
摘要
Antiretroviral therapy controls, but does not cure, HIV-1 infection due to a reservoir of rare CD4(+) T cells harboring latent proviruses. Little is known about the transcriptional program of latent cells. Here, we report a strategy to enrich clones of latent cells carrying intact, replication-competent HIV-1 proviruses from blood based on their expression of unique T cell receptors. Latent cell enrichment enabled single-cell transcriptomic analysis of 1,050 CD4(+) T cells belonging to expanded clones harboring intact HIV-1 proviruses from 6 different individuals. The analysis reveals that most of these cells are T effector memory cells that are enriched for expression of HLA-DR, HLA-DP, CD74, CCL5, granzymes A and K, cystatin F, LYAR, and DUSP2. We conclude that expanded clones of latent cells carrying intact HIV-1 proviruses persist preferentially in a distinct CD4(+) T cell population, opening possibilities for eradication.
引用
收藏
页数:21
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