Identification of CD98 as a Novel Biomarker for HIV-1 Permissiveness and Latent Infection.
Wanying ZhangMo ZhouCancan ChenShiyu WuLilin WangBaijin XiaJun LiuXiancai MaTing PanHui ZhangLinghua LiBingfeng LiuPublished in: mBio (2022)
Human immunodeficiency virus type 1 (HIV-1) can integrate viral DNA into host cell chromosomes to establish a long-term stable latent reservoir, which is a major obstacle to cure HIV-1 infection. The characteristics of the HIV-1 latent reservoir have not been fully understood. Here, we identified 126 upregulated plasma membrane proteins in HIV-1 latently infected cells by a label-free liquid chromatography-tandem mass spectrometry analysis. The higher levels of CD98 expression in multiple HIV-1 latently infected cell lines and primary CD4 + T cells compared to uninfected cells were further confirmed by quantitative reverse transcription PCR (RT-qPCR) and flow cytometry analyses. In addition, CD98 high CD4 + T cells displayed hyper-permissiveness to HIV-1 infection and possessed distinct immune phenotypic profiles associated with Th17 and peripheral follicular T helper (pTFH) characteristics. Notably, the CD98 high resting memory CD4 + T cells harbored significantly higher cell-associated viral RNA and intact provirus than CD98 low counterparts in HIV-1-infected individuals receiving combined antiretroviral therapy. Furthermore, CD98 high CD4 + T cells exhibited a robust proliferative capacity and significantly contributed to the clonal expansion of the HIV-1 latent reservoir. Our study demonstrates that CD98 can be used as a novel biomarker of HIV-1 latently infected cells to indicate the effect of various strategies to reduce the viral reservoir. IMPORTANCE Identification of cellular biomarkers is the crucial challenge to eradicate the HIV-1 latent reservoir. In our study, we identified CD98 as a novel plasma membrane biomarker for HIV-1 permissiveness and latent infection. Importantly, CD98 high CD4 + T cells exhibited a hyper-permissiveness to HIV-1 infection and significantly contributed to the clonal expansion of the HIV-1 latent reservoir. CD98 could be targeted to develop therapeutic strategies to reduce the HIV-1 latent reservoir in further research.
Keyphrases
- antiretroviral therapy
- hiv infected
- human immunodeficiency virus
- hiv positive
- hiv aids
- hiv infected patients
- hiv testing
- hepatitis c virus
- men who have sex with men
- single cell
- liquid chromatography tandem mass spectrometry
- sars cov
- cell death
- induced apoptosis
- mass spectrometry
- ms ms
- flow cytometry
- single molecule
- long non coding rna
- stem cells
- cell cycle arrest
- blood pressure
- heart rate
- dendritic cells
- drug delivery
- bone marrow
- water quality
- regulatory t cells
- circulating tumor