Lotter Hannelore, Rüssmann Holger, Heesemann Jürgen, Tannich Egbert
Bernhard-Nocht Institut für Tropenmedizin, Bernhard-Nocht-Strasse 74, D-20359 Hamburg, Germany.
Int J Med Microbiol. 2008 Jan;298(1-2):79-86. doi: 10.1016/j.ijmm.2007.07.001. Epub 2007 Sep 27.
Various attenuated Yersinia enterocolitica strains expressing different sections of the Entamoeba histolytica surface lectin via the type III protein secretion system (T3SS) were assessed for their use to orally vaccinate rodents against invasive amoebiasis. The T3SS was found to efficiently express and secrete or translocate subfragments as well as the entire heavy subunit of the lectin. Oral vaccination with recombinant Yersinia conferred significant protection against amoebic liver abscess formation when the antigen was expressed as a fusion molecule with the translocation domain of Yersinia outer protein E. However, effectiveness of vaccination was dependent on gender and the rodent species used. Protection was mediated primarily by cellular immune mechanisms as it was independent from the antibody titre against the amoeba lectin but correlated with an antigen-specific Th1-cytokine response. The results suggest that gram-negative bacteria expressing E. histolytica antigens via T3SS may constitute a suitable oral vaccine carrier against amoebiasis and that an effective IFN-gamma response is required for protection against invasive amoebiasis.
通过III型蛋白分泌系统(T3SS)表达溶组织内阿米巴表面凝集素不同片段的各种减毒小肠结肠炎耶尔森菌菌株,被评估用于经口给啮齿动物接种疫苗以预防侵袭性阿米巴病。发现T3SS能有效表达、分泌或转运凝集素的亚片段以及整个重链亚基。当抗原与耶尔森菌外膜蛋白E的转运结构域作为融合分子表达时,用重组耶尔森菌进行口服疫苗接种可显著预防阿米巴肝脓肿的形成。然而,疫苗接种的有效性取决于性别和所用的啮齿动物种类。保护主要由细胞免疫机制介导,因为它独立于针对阿米巴凝集素的抗体滴度,但与抗原特异性Th1细胞因子反应相关。结果表明,通过T3SS表达溶组织内阿米巴抗原的革兰氏阴性菌可能构成一种合适的抗阿米巴病口服疫苗载体,并且有效的IFN-γ反应是预防侵袭性阿米巴病所必需的。