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局部阴道内给予微囊化白细胞介素 12 增强淋病奈瑟菌的适应性免疫。

Enhancement of adaptive immunity to Neisseria gonorrhoeae by local intravaginal administration of microencapsulated interleukin 12.

机构信息

Department of Microbiology and Immunology, Witebsky Center for Microbial Pathogenesis and Immunology, University at Buffalo, New York.

出版信息

J Infect Dis. 2013 Dec 1;208(11):1821-9. doi: 10.1093/infdis/jit354. Epub 2013 Sep 18.

Abstract

Gonorrhea remains one of the most frequent infectious diseases, and Neisseria gonorrhoeae is emerging as resistant to most available antibiotics, yet it does not induce a state of specific protective immunity against reinfection. Our recent studies have demonstrated that N. gonorrhoeae proactively suppresses host T-helper (Th) 1/Th2-mediated adaptive immune responses, which can be manipulated to generate protective immunity. Here we show that intravaginally administered interleukin 12 (IL-12) encapsulated in sustained-release polymer microspheres significantly enhanced both Th1 and humoral immune responses in a mouse model of genital gonococcal infection. Treatment of mice with IL-12 microspheres during gonococcal challenge led to faster clearance of infection and induced resistance to reinfection, with the generation of gonococcus-specific circulating immunoglobulin G and vaginal immunoglobulin A and G antibodies. These results suggest that local administration of microencapsulated IL-12 can serve as a novel therapeutic and prophylactic strategy against gonorrhea, with implications for the development of an effective vaccine.

摘要

淋病仍然是最常见的传染病之一,淋病奈瑟菌对大多数可用的抗生素产生耐药性,但它不会诱导针对再次感染的特异性保护性免疫。我们最近的研究表明,淋病奈瑟菌主动抑制宿主辅助性 T 细胞 (Th)1/Th2 介导的适应性免疫反应,而这些反应可以被操纵以产生保护性免疫。在这里,我们显示阴道内给予包封在缓释聚合物微球中的白细胞介素 12 (IL-12) 可显著增强生殖器淋病奈瑟菌感染小鼠模型中的 Th1 和体液免疫反应。在淋球菌攻击期间用 IL-12 微球治疗小鼠可导致更快地清除感染,并诱导对再次感染的抵抗力,产生淋病奈瑟菌特异性循环免疫球蛋白 G 和阴道免疫球蛋白 A 和 G 抗体。这些结果表明,微囊化 IL-12 的局部给药可以作为一种针对淋病的新型治疗和预防策略,这对开发有效的疫苗具有重要意义。

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