Laboratory of Vaccinology and Mucosal Immunity, Université Libre de Bruxelles, 1070 Brussels, Belgium.
Université de Lille, CNRS, Inserm, CHU Lille, Institut Pasteur de Lille, U1019-UMR 8204-Center for Infection and Immunity of Lille, F-59000 Lille, France; and.
J Immunol. 2020 Apr 1;204(7):1715-1723. doi: 10.4049/jimmunol.1901214. Epub 2020 Mar 2.
T cell epitopes are mostly nonmodified peptides, although posttranslationally modified peptide epitopes have been described, but they originated from viral or self-proteins. In this study, we provide evidence of a bacterial methylated T cell peptide epitope. The mycobacterial heparin-binding hemagglutinin (HBHA) is a protein Ag with a complex C-terminal methylation pattern and is recognized by T cells from humans latently infected with By comparing native HBHA with recombinant HBHA produced in (rHBHA-), we could link antigenic differences to differences in the methylation profile. Peptide scan analyses led to the discovery of a peptide containing methyl lysines recognized by a mAb that binds to native HBHA ∼100-fold better than to rHBHA- This peptide was also recognized by T cells from latently infected humans, as evidenced by IFN-γ release upon peptide stimulation. The nonmethylated peptide did not induce IFN-γ, arguing that the methyl lysines are part of the T cell epitope.
T 细胞表位大多是非修饰的肽,尽管已经描述了翻译后修饰的肽表位,但它们来源于病毒或自身蛋白。在这项研究中,我们提供了细菌甲基化 T 细胞肽表位的证据。分枝杆菌肝素结合血凝素(HBHA)是一种具有复杂 C 末端甲基化模式的蛋白 Ag,可被潜伏感染的人类 T 细胞识别。通过比较天然 HBHA 与在 中产生的重组 HBHA(rHBHA-),我们可以将抗原差异与甲基化模式的差异联系起来。肽扫描分析导致发现了一种含有甲基赖氨酸的肽,该肽被一种 mAb 识别,该 mAb 与天然 HBHA 的结合比 rHBHA-强约 100 倍。该肽也被潜伏感染的人类 T 细胞识别,证据是在肽刺激下释放 IFN-γ。非甲基化肽不会诱导 IFN-γ,这表明甲基赖氨酸是 T 细胞表位的一部分。