Vordermeier H M, Zhu X, Harris D P
MRC Clinical Sciences Centre, Tuberculosis & Related Infections Unit, Hammersmith Hospital, London, UK.
Scand J Immunol. 1997 May;45(5):521-6. doi: 10.1046/j.1365-3083.1997.d01-432.x.
Mycobacterium tuberculosis is the single, most important cause of morbidity attributable to a single infectious organism. CD8+ T cells play an important role in anti-tuberculous immune responses in both mice and humans. Data concerning the identity of mycobacterial antigens recognized by CD8+ T cells is limited; consequently, few CTL epitopes have been characterized. The authors identified allele-specific (H-2b and d) MHC class I binding motifs in six prominent M. tuberculosis protein antigens (the 19 and 38 kDa lipoglycoproteins and the 10, 16, 65 and 70 kDa stress proteins). These predicted epitopes were tested for MHC binding as well as their ability to elicit peptide-specific CTL following in vivo priming. The authors were able to identify eight previously undescribed mycobacterial CTL epitopes by using spleen cells from peptide-immunized mice. In addition, CTL specific for at least one of these epitopes also recognized the naturally processed epitope presented on transfected EL4 target cells. These mycobacteria-derived CTL epitopes could be important for future analysis of the involvement of CD8+ T cells in M. tuberculosis infection, pathogenesis and vaccine development.
结核分枝杆菌是由单一感染性生物体导致发病的最重要的单一病因。CD8 + T细胞在小鼠和人类的抗结核免疫反应中均发挥重要作用。关于CD8 + T细胞识别的分枝杆菌抗原的特性的数据有限;因此,很少有CTL表位得到鉴定。作者在六种主要的结核分枝杆菌蛋白抗原(19 kDa和38 kDa脂糖蛋白以及10 kDa、16 kDa、65 kDa和70 kDa应激蛋白)中鉴定出等位基因特异性(H - 2b和d)MHC I类结合基序。对这些预测的表位进行了MHC结合测试以及体内激发后引发肽特异性CTL的能力测试。作者通过使用来自肽免疫小鼠的脾细胞,能够鉴定出八个先前未描述的分枝杆菌CTL表位。此外,针对这些表位中至少一个的CTL也识别转染的EL4靶细胞上呈递的天然加工表位。这些分枝杆菌衍生的CTL表位对于未来分析CD8 + T细胞在结核分枝杆菌感染、发病机制和疫苗开发中的作用可能很重要。