Juno Jennifer A, Eriksson Emily M
Department of Microbiology and Immunology The University of Melbourne at The Peter Doherty Institute for Infection and Immunity Melbourne VIC Australia.
Division of Population Health and Immunity Walter and Eliza Hall Institute of Medical Science Melbourne VIC Australia.
Clin Transl Immunology. 2019 Jul 17;8(7):e01069. doi: 10.1002/cti2.1069. eCollection 2019.
HIV infection is associated with a rapid and sustained inversion of the Vδ1:Vδ2 T-cell ratio in peripheral blood. Studies of antiretroviral therapy (ART)-treated cohorts suggest that ART is insufficient to reconstitute either the frequency or function of the γδ T-cell subset. Recent advances are now beginning to shed light on the relationship between microbial translocation, chronic inflammation, immune ageing and γδ T-cell immunology. Here, we review the impact of acute, chronic untreated and treated HIV infection on circulating and mucosal γδ T-cell subsets and highlight novel approaches to harness γδ T cells as components of anti-HIV immunotherapy.
HIV感染与外周血中Vδ1:Vδ2 T细胞比例的快速且持续倒置有关。对抗逆转录病毒疗法(ART)治疗队列的研究表明,ART不足以重建γδ T细胞亚群的频率或功能。最近的进展开始揭示微生物易位、慢性炎症、免疫衰老与γδ T细胞免疫学之间的关系。在此,我们综述急性、慢性未治疗和治疗的HIV感染对循环和黏膜γδ T细胞亚群的影响,并强调将γδ T细胞作为抗HIV免疫疗法组成部分的新方法。