D'Orazio Sarah E F, Shaw Christine A, Starnbach Michael N
Department of Microbiology, University of Kentucky College of Medicine, Lexington, KY 40536, USA.
J Exp Med. 2006 Feb 20;203(2):383-91. doi: 10.1084/jem.20052256. Epub 2006 Feb 6.
Studies using major histocompatibility complex (MHC)-Ia-deficient mice have shown that MHC-Ib-restricted CD8+ T cells can clear infections caused by intracellular pathogens such as Listeria monocytogenes. M3-restricted CD8+ T cells, which recognize short hydrophobic N-formylated peptides, appear to comprise a substantial portion of the MHC-Ib-restricted T cell response in the mouse model of L. monocytogenes infection. In this study, we isolated formyltransferase (fmt) mutant strains of L. monocytogenes that lacked the ability to add formyl groups to nascent polypeptides. These fmt mutant Listeria strains did not produce antigens that could be recognized by M3-restricted T cells. We showed that immunization of MHC-Ia-deficient mice with fmt mutant Listeria resulted in stimulation of a protective memory response that cleared subsequent challenge with wild-type L. monocytogenes, despite the fact that M3-restricted CD8+ T cells did not proliferate in these mice. These data suggest that M3-restricted T cells are not required for protection against L. monocytogenes and underscore the importance of searching for new antigen-presenting molecules among the large MHC-Ib family of proteins.
使用主要组织相容性复合体(MHC)-Ia缺陷小鼠的研究表明,MHC-Ib限制性CD8 + T细胞可以清除由细胞内病原体如单核细胞增生李斯特菌引起的感染。识别短疏水N-甲酰化肽的M3限制性CD8 + T细胞似乎在单核细胞增生李斯特菌感染的小鼠模型中占MHC-Ib限制性T细胞反应的很大一部分。在本研究中,我们分离出了缺乏向新生多肽添加甲酰基能力的单核细胞增生李斯特菌甲酰转移酶(fmt)突变株。这些fmt突变李斯特菌菌株不产生可被M3限制性T细胞识别的抗原。我们表明,用fmt突变李斯特菌免疫MHC-Ia缺陷小鼠会刺激产生保护性记忆反应,该反应可清除随后野生型单核细胞增生李斯特菌的攻击,尽管M3限制性CD8 + T细胞在这些小鼠中并未增殖。这些数据表明,针对单核细胞增生李斯特菌的保护不需要M3限制性T细胞,并强调了在庞大的MHC-Ib蛋白家族中寻找新的抗原呈递分子的重要性。