Soloski M J, Metcalf E S
Division of Rheumatology, Department of Medicine, The Johns Hopkins University School of Medicine, Baltimore, MD 21218, USA.
Microbes Infect. 2001 Nov-Dec;3(14-15):1249-59. doi: 10.1016/s1286-4579(01)01485-x.
Class I molecules with limited polymorphism have been implicated in the host response to infectious agents. Following infection with Salmonella typhimurium, mice develop a CD8+ CTL response that specifically recognizes bacteria infected cells. An immunodominant component of the CTL response recognizes a peptide epitope derived from the Salmonella GroEL molecule that is presented by the non-polymorphic MHC class Ib molecule Qa-1. T cells recognizing the bacterial peptide also cross-recognize a homologous peptide from the mammalian hsp60 molecule. Since Qa-1 has a functional equivalent in humans, this observation may be relevant not only to the host response involved in clearing infection but also in understanding the link between infection with Gram-negative pathogens and autoimmune disease.
具有有限多态性的I类分子与宿主对感染因子的反应有关。感染鼠伤寒沙门氏菌后,小鼠会产生一种CD8 + CTL反应,该反应能特异性识别被细菌感染的细胞。CTL反应的一个免疫显性成分识别来自沙门氏菌GroEL分子的肽表位,该表位由非多态性的MHC Ib类分子Qa-1呈递。识别细菌肽的T细胞也能交叉识别来自哺乳动物hsp60分子的同源肽。由于Qa-1在人类中有功能等效物,这一观察结果不仅可能与清除感染所涉及的宿主反应有关,还与理解革兰氏阴性病原体感染与自身免疫性疾病之间的联系有关。