Campbell D J, Shastri N
Department of Molecular and Cell Biology, University of California, Berkeley 94720-3200, USA.
J Immunol. 1998 Sep 1;161(5):2339-47.
Optimal immunity to the Gram-positive pathogen Listeria monocytogenes (LM) requires both CD8+ and CD4+ antigen-specific T cell responses. Understanding how CD4+ T cells function in an immune response to LM and how bacterial proteins are processed to peptide/MHC class II complexes in infected cells requires identification of these proteins. Using LacZ-inducible, LM-specific CD4+ T cells as probes, we identified two immunogenic LM proteins by a novel expression cloning strategy. The antigenic peptides contained within these proteins were defined by deletion analysis of the genes, and their antigenicity was confirmed with synthetic peptides. The nucleotide sequences of the genes showed that they encode previously unknown LM proteins that are homologous to surface proteins in other bacterial species. Consistent with their surface topology, mild trypsin treatment of LM protoplasts ablated T cell recognition of these Ags. These findings establish a general strategy for identifying unknown CD4+ T cell Ags and demonstrate that LM surface proteins can provide the peptides for presentation by MHC class II molecules that are specific targets for CD4+ T cells during murine LM infection.
对革兰氏阳性病原体单核细胞增生李斯特菌(LM)的最佳免疫需要CD8 +和CD4 +抗原特异性T细胞反应。了解CD4 + T细胞在对LM的免疫反应中如何发挥作用,以及细菌蛋白在受感染细胞中如何加工成肽/MHC II类复合物,需要鉴定这些蛋白质。我们使用LacZ诱导的、LM特异性CD4 + T细胞作为探针,通过一种新的表达克隆策略鉴定了两种免疫原性LM蛋白。通过对基因的缺失分析确定了这些蛋白中所含的抗原肽,并用合成肽证实了它们的抗原性。基因的核苷酸序列表明,它们编码以前未知的LM蛋白,这些蛋白与其他细菌物种的表面蛋白同源。与它们的表面拓扑结构一致,用温和的胰蛋白酶处理LM原生质体消除了T细胞对这些抗原的识别。这些发现建立了一种鉴定未知CD4 + T细胞抗原的通用策略,并证明LM表面蛋白可以提供肽,以供MHC II类分子呈递,这些肽是小鼠LM感染期间CD4 + T细胞的特异性靶标。