Méndez-Samperio P, Jiménez-Zamudio L
Departamento de Immunología, Escuela Nacional de Ciencias Biológicas, I.P.N., Carpio y Plan de Ayala, México, D.F., Mexico.
Rev Latinoam Microbiol. 1993 Oct-Dec;35(4):443-9.
It has been suggested that the cellular immune response to mycobacterial antigens, is implicated in the pathogenicity of inflammatory joint diseases such as rheumatoid arthritis. Therefore, the aim of this study was to identify T-cell epitopes in a series of 20-mer peptides spanning the entire 19-kDa protein of M. tuberculosis. Mononuclear cells obtained from six rheumatoid arthritis (RA) patients, were analyzed for their proliferation to both the 19-kDa containing immunoblot fraction and to the synthetic peptides. Mononuclear cells from three rheumatoid arthritis patients responded in a dose-dependent manner to peptides 1-20, 60-79, 71-90, 82-101, 90-109 and 121-140, whereas the other eight peptides: 11-30, 21-40, 41-60, 50-69, 100-119, 112-131, 131-150 and 140-159 did not stimulate significant proliferative responses in any of the patients tested. These results indicate, for the first time, the presence of dominant epitopes in the cellular immune response to the 19-kDa M. tuberculosis antigen by rheumatoid T cells.
有人提出,针对分枝杆菌抗原的细胞免疫反应与类风湿关节炎等炎性关节疾病的致病性有关。因此,本研究的目的是在一系列覆盖结核分枝杆菌整个19 kDa蛋白的20肽中鉴定T细胞表位。对从6名类风湿关节炎(RA)患者获得的单核细胞进行分析,观察其对含19 kDa的免疫印迹组分和合成肽的增殖反应。来自3名类风湿关节炎患者的单核细胞对肽1 - 20、60 - 79、71 - 90、82 - 101、90 - 109和121 - 140呈剂量依赖性反应,而其他8种肽:11 - 30、21 - 40、41 - 60、50 - 69、100 - 119、112 - 131、131 - 150和140 - 159在任何受试患者中均未刺激显著的增殖反应。这些结果首次表明,类风湿T细胞对结核分枝杆菌19 kDa抗原的细胞免疫反应中存在显性表位。