Department of Pulmonary and Critical Care Medicine, Oregon Health & Science University, Portland, OR, USA.
Division of Infection and Immunity, Cardiff University School of Medicine, Heath Park, Cardiff, UK.
Immunol Cell Biol. 2020 Oct;98(9):770-781. doi: 10.1111/imcb.12370. Epub 2020 Jul 12.
Mucosal-associated invariant T (MAIT) cells are key players in the immune response against microbial infection. The MAIT T-cell receptor (TCR) recognizes a diverse array of microbial ligands, and recent reports have highlighted the variability in the MAIT TCR that could further contribute to discrimination of ligand. The MAIT TCR complementarity determining region (CDR)3β sequence displays a high level of diversity across individuals, and clonotype usage appears to be dependent on antigenic exposure. To address the relationship between the MAIT TCR and microbial ligand, we utilized a previously defined panel of MAIT cell clones that demonstrated variability in responses against different microbial infections. Sequencing of these clones revealed four pairs, each with shared (identical) CDR3α and different CDR3β sequences. These pairs demonstrated varied responses against microbially infected dendritic cells as well as against 5-(2-oxopropylideneamino)-6-d-ribitylaminouracil, a ligand abundant in Salmonella enterica serovar Typhimurium, suggesting that the CDR3β contributes to differences in ligand discrimination. Taken together, these results highlight a key role for the MAIT CDR3β region in distinguishing between MR1-bound antigens and ligands.
黏膜相关恒定 T(MAIT)细胞是针对微生物感染的免疫反应的关键参与者。MAIT T 细胞受体(TCR)识别多种微生物配体,最近的报告强调了 MAIT TCR 的可变性,这可能进一步有助于配体的区分。MAIT TCR 互补决定区(CDR)3β序列在个体之间表现出高度的多样性,而且克隆型的使用似乎依赖于抗原暴露。为了解 MAIT TCR 与微生物配体之间的关系,我们利用了先前定义的 MAIT 细胞克隆面板,这些克隆对不同的微生物感染表现出不同的反应。对这些克隆的测序揭示了四对,每对都具有共享(相同)的 CDR3α和不同的 CDR3β序列。这些对在针对微生物感染的树突状细胞以及 5-(2-氧代丙基氨基)-6-d-核糖基氨基尿嘧啶(大量存在于沙门氏菌肠炎 Typhimurium 的配体)的反应中表现出不同,表明 CDR3β有助于区分配体。总之,这些结果突出了 MAIT CDR3β 区域在区分 MR1 结合抗原和配体方面的关键作用。