Mucosal-associated invariant T cells: A cryptic coordinator in HIV-infected immune reconstitution.
Bin SuDeshenyue KongXiaodong YangTong ZhangYi-Qun KuangPublished in: Journal of medical virology (2022)
Human immunodeficiency virus type 1 (HIV-1) infection causes considerable morbidity and mortality worldwide. Although antiretroviral therapy (ART) has largely transformed HIV infection from a fatal disease to a chronic condition, approximately 10%-40% of HIV-infected individuals who receive effective ART and sustain long-term viral suppression still cannot achieve optimal immune reconstitution. These patients are called immunological nonresponders, a state associated with poor clinical prognosis. Mucosal-associated invariant T (MAIT) cells are an evolutionarily conserved unconventional T-cell subset defined by expression of semi-invariant αβ T-cell receptor (TCR), which recognizes metabolites derived from the riboflavin biosynthetic pathway presented on major histocompatibility complex-related protein-1. MAIT cells, which are considered to act as a bridge between innate and adaptive immunity, produce a wide range of cytokines and cytotoxic molecules upon activation through TCR-dependent and TCR-independent mechanisms, which is of major importance in defense against a variety of pathogens. In addition, MAIT cells are involved in autoimmune and immune-mediated diseases. The number of MAIT cells is dramatically and irreversibly decreased in the early stage of HIV infection and is not fully restored even after long-term suppressive ART. In light of the important role of MAIT cells in mucosal immunity and because microbial translocation is inversely associated with CD4 + T-cell counts, we propose that MAIT cells participate in the maintenance of intestinal barrier integrity and microbial homeostasis, thus further affecting immune reconstitution in HIV-infected individuals.
Keyphrases
- antiretroviral therapy
- hiv infected
- human immunodeficiency virus
- induced apoptosis
- cell cycle arrest
- early stage
- hiv positive
- hiv aids
- hiv infected patients
- endoplasmic reticulum stress
- immune response
- cell death
- signaling pathway
- microbial community
- oxidative stress
- radiation therapy
- hepatitis c virus
- transcription factor
- multidrug resistant
- dendritic cells
- lymph node
- squamous cell carcinoma
- antimicrobial resistance