Lauvau Grégoire, Glaichenhaus Nicolas
Institut National de la Santé et de la Recherche Médicale, Valbonne, France.
Eur J Immunol. 2004 Apr;34(4):913-20. doi: 10.1002/eji.200424944.
Most intracellular pathogens induce robust T cell responses upon infection of mammalian hosts. In most cases, these T cell responses are protective and result in pathogen clearance. It is therefore important to determine how T cells are primed and how they differentiate into cytokine-secreting and/or cytotoxic effector cells. In contrast to B cells, which recognize soluble Ag, CD8(+) and CD4(+) T cells react to Ag-derived peptides bound to MHC I or MHC II molecules, respectively. Therefore, elucidating the mechanisms by which pathogen-derived Ag become available for presentation is necessary to understand how pathogens trigger T cell responses in vivo. Although many excellent reviews have focused on the mechanisms involved in Ag processing, very few have pointed to the specificity of host-pathogen interactions. In this respect, it should be noticed that these interactions are very different from one pathogen to another, and may result in the involvement of different cells and molecules. Because of space limitations, we have decided to focus this review on two intracellular pathogens--vaccinia virus and Listeria monocytogenes. We have chosen these two pathogens because they both induce a strong CD8(+) T cell response and because they have been extensively studied by both microbiologists and immunologists.
大多数细胞内病原体在感染哺乳动物宿主后会引发强烈的T细胞反应。在大多数情况下,这些T细胞反应具有保护性,并导致病原体清除。因此,确定T细胞如何被激活以及如何分化为分泌细胞因子和/或具有细胞毒性的效应细胞非常重要。与识别可溶性抗原的B细胞不同,CD8(+)和CD4(+) T细胞分别对与MHC I或MHC II分子结合的抗原衍生肽作出反应。因此,阐明病原体衍生的抗原如何可供呈递的机制对于理解病原体如何在体内触发T细胞反应是必要的。尽管许多优秀的综述都集中在抗原加工所涉及的机制上,但很少有综述指出宿主-病原体相互作用的特异性。在这方面,应该注意到这些相互作用因病原体而异,可能导致不同细胞和分子的参与。由于篇幅限制,我们决定将本综述的重点放在两种细胞内病原体——牛痘病毒和单核细胞增生李斯特菌上。我们选择这两种病原体是因为它们都能诱导强烈的CD8(+) T细胞反应,并且微生物学家和免疫学家都对它们进行了广泛的研究。