Lenz L L, Bevan M J
Howard Hughes Medical Institute, Department of Immunology, University of Washington, Seattle 98195, USA.
Immunol Rev. 1997 Aug;158:115-21. doi: 10.1111/j.1600-065x.1997.tb00997.x.
Cytotoxic T cells (CTL) play a critical role in the murine immune response to Listeria monocytogenes (Listeria). Bacterial antigens are presented to Listeria-specific CTL by products of both conventional, polymorphic MHC class Ia and non-polymorphic MHC class Ib alleles. The H2-M3 class Ib gene product, M3, preferentially presents formylmethionine-initiating (fMet) peptides derived from the N termini of bacterial and mitochondrial proteins. Thus, M3 signals the presence of bacterial invaders to CTL effectors. Listeria-encoded fMet peptide epitopes for H2-M3-restricted CTL have recently been identified. These and other identified fMet peptides are predominantly comprised of hydrophobic residues and appear to be cleaved from membrane-bound proteins. The subcellular location and membrane topology of such proteins may be significant factors in their selection as target antigens for H2-M3-restricted CTL. Such rules may prove useful for prediction of candidate fMet peptide epitopes from other bacterial proteins and species. Studies using synthetic fMet peptides to stimulate CTL ex vivo are also discussed. These latter studies indicate that Listeria infection boosts H2-M3-restricted CTL responses. However, in contrast to MHC class Ia-restricted CTL responses, fMet peptide-specific CTL are observed in a large proportion of cultures from non-immunized, conventionally housed (non-SPF) mice. The CTL activity in these latter cultures may reflect priming in vivo on cross-reactive antigens, or may indicate that requirements for priming of H2-M3-restricted CTL are less stringent than for class Ia-restricted responses.
细胞毒性T细胞(CTL)在小鼠对单核细胞增生李斯特菌(李斯特菌)的免疫反应中起关键作用。细菌抗原由传统的多态性MHC I类a型和非多态性MHC I类b型等位基因的产物呈递给李斯特菌特异性CTL。H2-M3 I类b基因产物M3优先呈递源自细菌和线粒体蛋白质N端的甲酰甲硫氨酸起始(fMet)肽。因此,M3向CTL效应细胞发出细菌入侵者存在的信号。最近已鉴定出针对H2-M3限制性CTL的李斯特菌编码的fMet肽表位。这些以及其他已鉴定的fMet肽主要由疏水残基组成,似乎是从膜结合蛋白上切割下来的。此类蛋白的亚细胞定位和膜拓扑结构可能是其被选为H2-M3限制性CTL靶抗原的重要因素。此类规则可能被证明有助于预测来自其他细菌蛋白和物种的候选fMet肽表位。还讨论了使用合成fMet肽在体外刺激CTL的研究。这些后期研究表明,李斯特菌感染可增强H2-M3限制性CTL反应。然而,与MHC I类a型限制性CTL反应不同,在来自未免疫、常规饲养(非无特定病原体)小鼠的大部分培养物中都观察到了fMet肽特异性CTL。这些后期培养物中的CTL活性可能反映了体内对交叉反应性抗原的致敏,或者可能表明引发H2-M3限制性CTL的要求比引发I类a型限制性反应的要求不那么严格。