From dendritic cells to B cells dysfunctions during HIV-1 infection: T follicular helper cells at the crossroads.
Nicolas RuffinLylia HaniNabila SeddikiPublished in: Immunology (2017)
T follicular helper (Tfh) cells are essential for B-cell differentiation and the subsequent antibody responses. Their numbers and functions are altered during human and simian immunodeficiency virus (HIV/SIV) infections. In lymphoid tissues, Tfh cells are present in germinal centre, where they are the main source of replicative HIV-1 and represent a major reservoir. Paradoxically, Tfh cell numbers are increased in chronically infected individuals. Understanding the fate of Tfh cells in the course of HIV-1 infection is essential for the design of efficient strategies toward a protective HIV vaccine or a cure. The purpose of this review is to summarize the recent advance in our understanding of Tfh cell dynamics during HIV/SIV infection. In particular, to explore the possible causes of their expansion in lymphoid tissues by discussing the impact of HIV-1 infection on dendritic cells, to identify the molecular players rendering Tfh cells highly susceptible to HIV-1 infection, and to consider the contribution of regulatory follicular T cells in shaping Tfh cell functions.
Keyphrases
- antiretroviral therapy
- induced apoptosis
- dendritic cells
- cell cycle arrest
- hiv infected
- hiv positive
- human immunodeficiency virus
- hepatitis c virus
- hiv aids
- immune response
- endoplasmic reticulum stress
- hiv testing
- endothelial cells
- cell therapy
- oxidative stress
- signaling pathway
- men who have sex with men
- cell proliferation
- stem cells
- single molecule