Skoberne M, Holtappels R, Hof H, Geginat G
Institut für Medizinische Mikrobiologie und Hygiene, Fakultät für Klinische Medizin Mannheim der Universität Heidelberg, Mannheim, Germany.
J Immunol. 2001 Aug 15;167(4):2209-18. doi: 10.4049/jimmunol.167.4.2209.
Little information exists regarding the presentation of antigenic peptides in infected tissues. In this study the in vivo presentation of four different CD8 T cell epitopes of Listeria monocytogenes was monitored. Peptide presentation was measured by a new, highly sensitive, ex vivo Ag presentation assay that was based on the testing of freshly isolated cells from infected spleens with peptide-specific CD8 T cell lines in an IFN-gamma-specific ELISPOT assay. Remarkably, the peptide presentation pattern of splenocytes and that of macrophages purified from spleens of L. monocytogenes-infected mice were different from those of in vitro infected macrophage-like cell lines. The in vivo Ag presentation pattern of splenocytes also exhibited dynamic changes during the first 48 h of infection. In vivo peptide presentation at later time points postinfection was biased toward immunodominant CD8 T cell epitopes, while at an early time point, 6 h postinfection, subdominant and dominant CD8 T cell epitopes were presented with similar strength. In summary, our studies show that Ag presentation during an infection is a highly dynamic process that only can be fully appreciated by the study of cells infected in their physiological environment.
关于感染组织中抗原肽的呈递情况,目前所知甚少。在本研究中,对单核细胞增生李斯特菌的四种不同CD8 T细胞表位的体内呈递情况进行了监测。肽呈递通过一种新的、高度灵敏的体外抗原呈递测定法进行测量,该方法基于在干扰素-γ特异性酶联免疫斑点测定法中,用肽特异性CD8 T细胞系对从感染脾脏中新鲜分离的细胞进行检测。值得注意的是,从单核细胞增生李斯特菌感染小鼠脾脏中纯化的脾细胞和巨噬细胞的肽呈递模式,与体外感染的巨噬细胞样细胞系不同。脾细胞的体内抗原呈递模式在感染的最初48小时内也呈现出动态变化。感染后较晚时间点的体内肽呈递偏向于免疫显性CD8 T细胞表位,而在感染后6小时的早期时间点,亚显性和显性CD8 T细胞表位以相似的强度呈递。总之,我们的研究表明,感染期间的抗原呈递是一个高度动态的过程,只有通过研究在其生理环境中被感染的细胞才能充分理解。