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口服或鼻内接种弗氏志贺菌2a和宋内志贺菌蛋白酶体-脂多糖疫苗在动物模型中的免疫原性和效力

Immunogenicity and efficacy of oral or intranasal Shigella flexneri 2a and Shigella sonnei proteosome-lipopolysaccharide vaccines in animal models.

作者信息

Orr N, Robin G, Cohen D, Arnon R, Lowell G H

机构信息

Medical Corps, Israel Defence Force, Rehovot.

出版信息

Infect Immun. 1993 Jun;61(6):2390-5. doi: 10.1128/iai.61.6.2390-2395.1993.

Abstract

Immunity against shigellosis has been shown to correlate with the presence of antibodies specific for Shigella lipopolysaccharide (LPS). We here propose a new candidate vaccine for shigellosis composed of purified Shigella flexneri 2a or Shigella sonnei LPS hydrophobically complexed with group C type 2b Neisseria meningitidis outer membrane protein proteosomes. Immunization of mice either orally or intranasally with this complex induced specific homologous anti-LPS antibodies in both intestinal and respiratory secretions as well as in sera. Strong anamnestic responses were found after two or three immunizations. LPS alone, alkaline-detoxified LPS, or alkaline-detoxified LPS complexed with proteosomes was not effective. Oral or intranasal immunization of guinea pigs with two or more doses of this proteosome-LPS vaccine elicited homologous protection against Shigella keratoconjunctivitis (Serény test). These data demonstrate that proteosomes can be used as an effective mucosal vaccine delivery system and that orally or intranasally administered acellular vaccines can protect against Shigella infections.

摘要

针对志贺氏菌病的免疫力已被证明与针对志贺氏菌脂多糖(LPS)的特异性抗体的存在相关。我们在此提出一种用于志贺氏菌病的新型候选疫苗,它由纯化的福氏志贺氏菌2a或宋内志贺氏菌LPS与C群2b型脑膜炎奈瑟菌外膜蛋白蛋白酶体进行疏水复合而成。用这种复合物对小鼠进行口服或鼻内免疫,可在肠道和呼吸道分泌物以及血清中诱导产生特异性同源抗LPS抗体。在进行两次或三次免疫后发现有强烈的回忆反应。单独的LPS、碱解毒LPS或与蛋白酶体复合的碱解毒LPS均无效。用两剂或更多剂这种蛋白酶体-LPS疫苗对豚鼠进行口服或鼻内免疫,可引发针对志贺氏菌性角膜结膜炎的同源保护作用(塞雷尼试验)。这些数据表明,蛋白酶体可作为一种有效的黏膜疫苗递送系统,并且口服或鼻内给药的无细胞疫苗可预防志贺氏菌感染。

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