Ussher James E, Phalora Prabhjeet, Cosgrove Cormac, Hannaway Rachel F, Rauch Andri, Günthard Huldrych F, Goulder Philip, Phillips Rodney E, Willberg Christian B, Klenerman Paul
From the Peter Medawar Building for Pathogen Research (JEU, PP, CC, PG, REP, CBW, PK), University of Oxford, Oxford, UK; Department of Microbiology and Immunology (JEU, RFH), University of Otago, Dunedin, New Zealand; Ragon Institute of MGH, MIT and Harvard (CC), Cambridge, Massachusetts, USA; Division of Infectious Diseases (AR), University Hospital Berne and University of Berne, Berne; Division of Infectious Diseases and Hospital Epidemiology and Institute of Medical Virology (HFG), University Hospital Zurich, University of Zurich, Zurich, Switzerland.
Medicine (Baltimore). 2015 Jul;94(29):e1134. doi: 10.1097/MD.0000000000001134.
Mucosal-associated invariant T (MAIT) cells are an abundant antibacterial innate-like lymphocyte population. There are conflicting reports as to their fate in HIV infection. The objective of this study was to determine whether MAIT cells are truly depleted in HIV infection. In this case-control study of HIV-positive patients and healthy controls, quantitative real-time polymerase chain reaction was used to assess the abundance of messenger RNA (mRNA) and genomic DNA (gDNA) encoding the canonical MAIT cell T cell receptor (Vα7.2-Jα33). Comparison was made with flow cytometry. Significant depletion of both Vα7.2-Jα33 mRNA and gDNA was seen in HIV infection. Depletion of Vα7.2+CD161++ T cells was confirmed by flow cytometry. In HIV infection, the abundance of Vα7.2-Jα33 mRNA correlated most strongly with the frequency of Vα7.2+CD161++ cells. No increase was observed in the frequency of Vα7.2+CD161- cells among CD3+CD4- lymphocytes. MAIT cells are depleted from blood in HIV infection as confirmed by independent assays. Significant accumulation of a CD161- MAIT cell population is unlikely. Molecular approaches represent a suitable alternative to flow cytometry-based assays for tracking of MAIT cells in HIV and other settings.
黏膜相关恒定T(MAIT)细胞是一类数量丰富的具有抗菌功能的固有样淋巴细胞群体。关于它们在HIV感染中的命运,存在相互矛盾的报道。本研究的目的是确定MAIT细胞在HIV感染中是否真的会减少。在这项针对HIV阳性患者和健康对照的病例对照研究中,采用定量实时聚合酶链反应来评估编码典型MAIT细胞T细胞受体(Vα7.2-Jα33)的信使核糖核酸(mRNA)和基因组DNA(gDNA)的丰度。并与流式细胞术进行比较。在HIV感染中,Vα7.2-Jα33 mRNA和gDNA均显著减少。通过流式细胞术证实了Vα7.2+CD161++ T细胞的减少。在HIV感染中,Vα7.2-Jα33 mRNA的丰度与Vα7.2+CD161++细胞的频率相关性最强。在CD3+CD4-淋巴细胞中,未观察到Vα7.2+CD161-细胞频率增加。独立检测证实,HIV感染会导致血液中MAIT细胞减少。CD161- MAIT细胞群体不太可能显著积累。分子方法是在HIV及其他情况下追踪MAIT细胞的一种合适的替代流式细胞术检测的方法。