Darji A, Bruder D, zur Lage S, Gerstel B, Chakraborty T, Wehland J, Weiss S
Division of Cell Biology and Immunobiology, Gesellschaft für Biotechnologische Forschung-National Research Center for Biotechnology, Braunschweig, Germany.
J Immunol. 1998 Sep 1;161(5):2414-20.
ActA, an essential virulence factor of Listeria monocytogenes, is an integral membrane protein that is required for intracellular motility, cell-to-cell spread, and rapid dissemination of the bacteria in the infected host. To reveal cytotoxic T cell responses against ActA we introduced a recombinant soluble form of ActA into the MHC class I-processing compartment of APC using a variant of listeriolysin mutated within its immunodominant MHC class I epitope. With this experimental system we demonstrate that T cells are induced against ActA during a sublethal infection with L. monocytogenes. However, adoptively transferred cytotoxic CD8+ T cells specific for ActA did not protect mice against a subsequent challenge with this pathogen. This was due to an inability of APC to present ActA by either MHC class I or class II molecules as long as ActA remained tethered to the surface of intracellular viable bacteria. ActA was only presented when L. monocytogenes were engineered to secrete ActA or when the bacteria were killed by antibiotics during the assay. These findings raise questions on the general use of membrane proteins of pathogens as candidates for subunit vaccines.
内化素A(ActA)是单核细胞增生李斯特菌的一种重要毒力因子,是一种整合膜蛋白,对于细胞内运动、细胞间传播以及细菌在受感染宿主体内的快速扩散至关重要。为了揭示针对ActA的细胞毒性T细胞反应,我们使用在其免疫显性MHC I类表位内发生突变的李斯特菌溶血素变体,将重组可溶性形式的ActA引入抗原呈递细胞(APC)的MHC I类加工区室。通过这个实验系统,我们证明在单核细胞增生李斯特菌亚致死感染期间会诱导产生针对ActA的T细胞。然而,过继转移的针对ActA的细胞毒性CD8 + T细胞并不能保护小鼠免受该病原体的后续攻击。这是因为只要ActA仍与细胞内活细菌表面相连,APC就无法通过MHC I类或II类分子呈递ActA。只有当单核细胞增生李斯特菌被设计分泌ActA时,或者在检测过程中细菌被抗生素杀死时,ActA才会被呈递。这些发现对将病原体膜蛋白用作亚单位疫苗候选物的普遍应用提出了疑问。