HIV-1 reservoir dynamics in CD4+T cells

被引:0
|
作者
Bruner, Katherine M. [1 ]
Cohn, Lillian B. [2 ]
机构
[1] Univ Texas Austin, Dept Mol Biosci, Austin, TX 78712 USA
[2] Chan Zuckerberg Biohub, 499 Illinois St, San Francisco, CA 94158 USA
关键词
clonal expansion; HIV latency; HIV persistence; HIV reservoir; T cell proliferation; CD4(+) T-CELLS; LATENT RESERVOIR; ANTIRETROVIRAL THERAPY; PROLONGED SUPPRESSION; DECAY DYNAMICS; DNA; PROLIFERATION; PERSISTENCE; PROVIRUSES; VIREMIA;
D O I
10.1097/COH.0000000000000521
中图分类号
R392 [医学免疫学]; Q939.91 [免疫学];
学科分类号
100102 ;
摘要
Purpose of review To provide a summary of the recent data examining infected CD4+ T cell dynamics during ART and implications for cure strategies. Recent findings HIV-1 cure is a worldwide unmet medical need. Although combination antiretroviral therapies effectively suppress HIV-1 replication in vivo, viral rebound occurs shortly after therapy cessation. The major barrier to HIV-1 cure is a pool of latently infected CD4+ T cells, called the latent reservoir, which is established early during infection, has a long half-life in vivo, and is not eliminated by treatment. It was thought that the stability of the reservoir came from long-lived latently infected CD4+ T cells, but more recent data suggests that the reservoir is dynamic, such that there is an equilibrium in which proliferation of HIV-1-infected cells is offset by an equivalent loss of cells harboring HIV-1 DNA. Summary We review the evidence to support this dynamic model of persistence, mechanisms by which infected cells expand and are eliminated, and discuss the impact of a dynamic reservoir on the future of HIV-1 cure studies.
引用
收藏
页码:108 / 114
页数:7
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