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用SseB/鞭毛蛋白进行双重免疫可增强对循环记忆细胞介导的感染的保护作用。

Dual Immunization with SseB/Flagellin Provides Enhanced Protection against Infection Mediated by Circulating Memory Cells.

作者信息

Lee Seung-Joo, Benoun Joseph, Sheridan Brian S, Fogassy Zachary, Pham Oanh, Pham Quynh-Mai, Puddington Lynn, McSorley Stephen J

机构信息

Center for Comparative Medicine, School of Veterinary Medicine, University of California, Davis, Davis, CA 95616.

Department of Anatomy, Physiology, and Cell Biology, School of Veterinary Medicine, University of California Davis, Davis, CA 95616; and.

出版信息

J Immunol. 2017 Aug 15;199(4):1353-1361. doi: 10.4049/jimmunol.1601357. Epub 2017 Jul 14.

Abstract

The development of a subunit vaccine has been hindered by the absence of detailed information about antigenic targets of protective -specific T and B cells. Recent studies have identified SseB as a modestly protective Ag in susceptible C57BL/6 mice, but the mechanism of protective immunity remains undefined. In this article, we report that simply combining SseB with flagellin substantially enhances protective immunity, allowing immunized C57BL/6 mice to survive for up to 30 d following challenge with virulent bacteria. Surprisingly, the enhancing effect of flagellin did not require flagellin Ag targeting during secondary responses or recognition of flagellin by TLR5. Although coimmunization with flagellin did not affect SseB-specific Ab responses, it modestly boosted CD4 responses. In addition, protective immunity was effectively transferred in circulation to parabionts of immunized mice, demonstrating that tissue-resident memory is not required for vaccine-induced protection. Finally, protective immunity required host expression of IFN-γR but was independent of induced NO synthase expression. Taken together, these data indicate that flagellin has unique adjuvant properties that improve SseB-mediated protective immunity provided by circulating memory.

摘要

由于缺乏关于保护性特异性T细胞和B细胞抗原靶点的详细信息,亚单位疫苗的研发受到了阻碍。最近的研究已将SseB鉴定为对易感C57BL/6小鼠具有一定保护作用的抗原,但保护性免疫的机制仍不明确。在本文中,我们报告称,简单地将SseB与鞭毛蛋白结合可显著增强保护性免疫,使免疫后的C57BL/6小鼠在受到强毒细菌攻击后存活长达30天。令人惊讶的是,鞭毛蛋白的增强作用在二次反应期间不需要鞭毛蛋白抗原靶向或通过TLR5识别鞭毛蛋白。虽然与鞭毛蛋白共同免疫不影响SseB特异性抗体反应,但它适度增强了CD4反应。此外,保护性免疫在循环中有效地转移到了免疫小鼠的联体共生体中,这表明疫苗诱导的保护不需要组织驻留记忆。最后,保护性免疫需要宿主表达IFN-γR,但与诱导型一氧化氮合酶的表达无关。综上所述,这些数据表明鞭毛蛋白具有独特的佐剂特性,可改善由循环记忆提供的SseB介导的保护性免疫。

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