Tropical Infectious Diseases Research and Education Center (TIDREC), Department of Medical Microbiology, Faculty of Medicine, University of Malaya, Lembah Pantai, 50603 Kuala Lumpur, Malaysia; Center of Excellence for Research in AIDS (CERiA), University of Malaya, Lembah Pantai, 50603 Kuala Lumpur, Malaysia.
Department of Biomedical Science, Faculty of Medicine, University of Malaya, Lembah Pantai, 50603 Kuala Lumpur, Malaysia.
PLoS One. 2015 Apr 20;10(4):e0124659. doi: 10.1371/journal.pone.0124659. eCollection 2015.
Mucosal-associated invariant T (MAIT) cells are evolutionarily conserved antimicrobial MR1-restricted CD8(+) T cells co-expressing the semi-invariant TCR Vα7.2, and are numerous in the blood and mucosal tissues of humans. MAIT cells appear to undergo exhaustion in chronic viral infections. However, their role in human immunodeficiency virus type 1 (HIV-1) mono-infection and HIV/tuberculosis (TB) co-infection have seldom been elaborately investigated. We conducted a cross-sectional study to investigate the frequencies and phenotypes of CD161(++)CD8(+) T cells among anti-retroviral therapy (ART)/anti-TB therapy (ATT) treatment-naïve HIV/TB co-infected, ART/TB treated HIV/TB co-infected, ART naïve HIV-infected, ART-treated HIV-infected patients, and HIV negative healthy controls (HCs) by flow cytometry. Our data revealed that the frequency of MAIT cells was severely depleted in HIV mono- and HIV/TB co-infections. Further, PD-1 expression on MAIT cells was significantly increased in HIV mono- and HIV-TB co-infected patients. The frequency of MAIT cells did not show any significant increase despite the initiation of ART and/or ATT. Majority of the MAIT cells in HCs showed a significant increase in CCR6 expression as compared to HIV/TB co-infections. No marked difference was seen with expressions of chemokine co-receptor CCR5 and CD103 among the study groups. Decrease of CCR6 expression appears to explain why HIV-infected patients display weakened mucosal immune responses.
黏膜相关不变 T(MAIT)细胞是一种进化上保守的抗微生物 MR1 限制性 CD8+T 细胞,共表达半不变 TCR Vα7.2,在人类的血液和黏膜组织中数量众多。MAIT 细胞在慢性病毒感染中似乎会发生衰竭。然而,它们在人类免疫缺陷病毒 1 型(HIV-1)单一感染和 HIV/结核病(TB)合并感染中的作用很少被详细研究。我们进行了一项横断面研究,通过流式细胞术调查了抗逆转录病毒治疗(ART)/抗结核治疗(ATT)治疗初治的 HIV/TB 合并感染、ART/TB 治疗的 HIV/TB 合并感染、ART 初治的 HIV 感染、ART 治疗的 HIV 感染患者以及 HIV 阴性健康对照(HCs)中 CD161++CD8+T 细胞的频率和表型。我们的数据显示,MAIT 细胞在 HIV 单一感染和 HIV/TB 合并感染中严重耗竭。此外,PD-1 在 HIV 单一感染和 HIV/TB 合并感染患者的 MAIT 细胞上的表达显著增加。尽管开始了 ART 和/或 ATT,MAIT 细胞的频率并没有显著增加。与 HIV/TB 合并感染相比,HCs 中的大多数 MAIT 细胞显示出 CCR6 表达的显著增加。在研究组之间,趋化因子共受体 CCR5 和 CD103 的表达没有明显差异。CCR6 表达的下降似乎解释了为什么 HIV 感染患者显示出减弱的黏膜免疫反应。