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首页> 外文期刊>The Journal of Immunology: Official Journal of the American Association of Immunologists >HIV mucosal vaccine: nasal immunization with gp160-encapsulated hemagglutinating virus of Japan-liposome induces antigen-specific CTLs and neutralizing antibody responses.
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HIV mucosal vaccine: nasal immunization with gp160-encapsulated hemagglutinating virus of Japan-liposome induces antigen-specific CTLs and neutralizing antibody responses.

机译:HIV粘膜疫苗:用gp160封装的日本脂质体血凝病毒鼻腔免疫可诱导抗原特异性CTL并中和抗体反应。

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摘要

Nasal immunization of normal mice with HIVgp160-encapsulated hemagglutinating virus of Japan (HVJ)-liposome induced high titers of gp160-specific neutralizing IgG in serum and IgA in nasal wash, saliva, fecal extract, and vaginal wash, along with both Th1- and Th2-type responses. HIVgp160-specific IgG- and IgA-producing cells were also detected in mononuclear cells isolated from spleen, nasal cavity, salivary gland, intestinal lamina propria, and vaginal tissue of nasally immunized mice. In addition, CD8(+) CTLs were induced in mice nasally immunized with gp160-HVJ-liposome. These findings suggest that two layers of effective HIV-specific humoral and cellular immunity, in mucosal and systemic sites, were induced by this nasal vaccine. In immunodeficient mice, nasal immunization with gp160-HVJ-liposome induced Ag-specific immune responses for the systemic and mucosal compartments of both Th1 (IFN-gamma(-/-)) and Th2 (IL-4(-/-)). In vitro Ag-specific serum IgG Ab and vaginal wash samples possessing IgA and IgG Abs that had been induced by nasal immunization with gp160-HVJ-liposome were able to neutralize a clinically isolated strain of HIV-MN strain isolated from Japanese hemophiliac patients. Taken together, these results suggest that, for the prevention and control of AIDS, nasally administered gp160-HVJ-liposome is a powerful immunization tool that induces necessary Ag-specific immune responses at different stages of HIV infection.
机译:用HIVgp160封装的日本血凝病毒(脂质体)对正常小鼠进行鼻部免疫,可在鼻洗液,唾液,粪便和阴道洗液以及Th1-和Ng中诱导高滴度的血清和IgA中的gp160特异性中和IgG滴度Th2型反应。在分离自经免疫的小鼠的脾脏,鼻腔,唾液腺,固有层肠和阴道组织的单核细胞中,也检测到了产生HIVgp160特异性IgG和IgA的细胞。此外,在经gp160-HVJ-脂质体经鼻免疫的小鼠中诱导了CD8(+)CTL。这些发现表明,这种鼻疫苗可在粘膜和全身部位诱导出两层有效的HIV特异性体液和细胞免疫。在免疫缺陷小鼠中,用gp160-HVJ-脂质体进行鼻免疫可诱导针对Th1(IFN-γ(-/-))和Th2(IL-4(-/-))的全身和粘膜区室的Ag特异性免疫反应。已通过gp160-HVJ-脂质体经鼻免疫诱导的体外Ag特异性血清IgG Ab和具有IgA和IgG Abs的阴道清洗样品能够中和从日本血友病患者中分离出的HIV-MN株的临床分离株。综上所述,这些结果表明,对于艾滋病的预防和控制,经鼻给予gp160-HVJ-脂质体是一种强大的免疫工具,可在HIV感染的不同阶段诱导必要的Ag特异性免疫反应。

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