Kaufmann Stefan He, Schaible Ulrich E
Max-Planck-Institute for Infection Biology, Department of Immunology, Schumannstrasse 21-22, D-10117 Berlin, Germany.
Curr Opin Immunol. 2005 Feb;17(1):79-87. doi: 10.1016/j.coi.2004.12.004.
Antigen processing and recognition is a key feature of antibacterial immune responses to intracellular bacteria. In contrast to viruses, which are primarily controlled by conventional MHC II- and MHC I-restricted CD4+ or CD8+ T cells, respectively, unconventional T cells participate additionally in antibacterial protection. These unconventional T cells include glycolipid-specific CD1-restricted T cells and phospholigand-specific gammadelta T cells. We are just beginning to understand the broad spectrum of antigen recognition and stimulation of distinct T-cell populations by bacterial pathogens. From the host perspective, a broad spectrum of different T-cell populations that recognize proteins, lipids and carbohydrates strengthens protective immunity. From the perspective of the pathogen, antigen presentation represents a bottleneck that should be exploited for evasion from, or devastation of, acquired immunity. Although several such mechanisms have been described in viral systems, few have thus far been elucidated in bacterial infections.
抗原加工与识别是针对细胞内细菌的抗菌免疫反应的关键特征。与主要分别由传统的MHC II类和MHC I类限制的CD4+或CD8+ T细胞控制的病毒不同,非常规T细胞也参与抗菌保护。这些非常规T细胞包括糖脂特异性CD1限制的T细胞和磷脂配体特异性γδ T细胞。我们才刚刚开始了解细菌病原体对抗原的广泛识别以及对不同T细胞群体的刺激。从宿主的角度来看,广泛的不同T细胞群体识别蛋白质、脂质和碳水化合物可增强保护性免疫。从病原体的角度来看,抗原呈递是一个瓶颈,病原体可利用这一瓶颈来逃避或破坏获得性免疫。尽管在病毒系统中已经描述了几种这样的机制,但迄今为止在细菌感染中阐明的却很少。