aCenter for Infectious Medicine, Department of Medicine, Karolinska Institutet, Karolinska University Hospital Huddinge bCenter for HIV Research, Karolinska Institutet, Stockholm, Sweden cDepartment of Medical Microbiology and Immunology, School of Medicine, University of California Davis, Davis, California, USA.
AIDS. 2013 Oct 23;27(16):2501-4. doi: 10.1097/QAD.0b013e3283620726.
Mucosa-associated Invariant T (MAIT) cells are an evolutionarily conserved innate-like T cell subset that recognizes antigens presented by MR1 molecules. These antigens include vitamin B derivatives shared by many potentially pathogenic microbes, including and . It was recently discovered that MAIT cells decay numerically and functionally in HIV-1 infection, and that they fail to recover despite several years of effective suppression of viral replication by antiretroviral therapy (ART). Here, we briefly discuss the roles of MAIT cells and their loss in HIV immunopathogenesis. We furthermore propose that the persistence of MAIT cell loss on ART needs to be taken into account when assessing the immunological response to treatment, and when treatment should commence. The importance of this T cell subset in HIV-1 infection needs further study, and interventions to restore the MAIT cell compartment should be considered.
黏膜相关恒定 T(MAIT)细胞是一种进化上保守的先天样 T 细胞亚群,能够识别由 MR1 分子呈递的抗原。这些抗原包括许多潜在致病性微生物共有的维生素 B 衍生物,包括 和 。最近发现,MAIT 细胞在 HIV-1 感染中数量和功能下降,尽管抗逆转录病毒疗法(ART)能够有效抑制病毒复制多年,但它们仍无法恢复。在这里,我们简要讨论了 MAIT 细胞的作用及其在 HIV 免疫发病机制中的丧失。我们还提出,在评估治疗的免疫反应以及何时开始治疗时,需要考虑到 MAIT 细胞丧失在 ART 上的持续存在。这个 T 细胞亚群在 HIV-1 感染中的重要性需要进一步研究,并且应该考虑恢复 MAIT 细胞区室的干预措施。