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使用产肠毒素大肠杆菌定居因子CFA/I和CS6对BALB/c小鼠进行黏膜免疫,分别在有和没有突变型不耐热肠毒素的情况下给药。

Mucosal immunization of BALB/c mice using enterotoxigenic Escherichia coli colonization factors CFA/I and CS6 administered with and without a mutant heat-labile enterotoxin.

作者信息

Byrd Wyatt, Cassels Frederick J

机构信息

Department of Enteric Infections, Walter Reed Army Institute of Research, 503 Robert Grant Avenue, Silver Spring, MD 20910-7500, USA.

出版信息

Vaccine. 2003 May 16;21(17-18):1884-93. doi: 10.1016/s0264-410x(03)00014-8.

DOI:10.1016/s0264-410x(03)00014-8
PMID:12706673
Abstract

Mice (BALB/c) were intranasally (IN) and intragastrically (IG) administered the ETEC colonization factors (CF), CFA/I and CS6, with and without the R192G mutant heat-labile enterotoxin (mLT), and immunogenicity and efficacy measured. The IN administration of CFA/I to mice induced strong serum and fecal IgG and IgA responses. The IG administration of CFA/I to mice induced serum IgG and fecal IgA responses, but only when mLT was co-administered with CFA/I were serum IgA titers detected. The IN administration of CS6 to mice induced serum IgG antibodies, and mLT, when co-administered with CS6, enhanced the serum IgG response. Only when the mLT was co-administered with CS6, were serum and fecal IgA responses detected. The IG administration of CS6 plus mLT induced serum IgG and fecal IgA responses. Partial protection against lethal challenge with ETEC strain H10407 was seen in the mice IN administered the CFA/I plus mLT (P<0.01), and H10407 was cleared from the lungs of CFA/I plus mLT-immunized mice at a significantly greater rate than from the control mice (P<0.05). CFA/I and CS6 administered IN and IG induced mixed Th1/Th2 immune responses with the Th2 type being predominant as evidenced by IgG1>IgG2a. The administration of colonization factors to mice, particularly by the IN route, potentially serves as a useful way to measure the serum and mucosal immune responses to these antigens prior to their use in volunteers.

摘要

将肠毒素大肠杆菌(ETEC)的定植因子(CF)、CFA/I和CS6经鼻内(IN)和胃内(IG)给予BALB/c小鼠,并同时给予或不给予R192G突变型不耐热肠毒素(mLT),然后检测免疫原性和效力。给小鼠经鼻内给予CFA/I可诱导强烈的血清和粪便IgG及IgA反应。给小鼠经胃内给予CFA/I可诱导血清IgG和粪便IgA反应,但只有当mLT与CFA/I共同给药时才能检测到血清IgA滴度。给小鼠经鼻内给予CS6可诱导血清IgG抗体,当mLT与CS6共同给药时,可增强血清IgG反应。只有当mLT与CS6共同给药时,才能检测到血清和粪便IgA反应。经胃内给予CS6加mLT可诱导血清IgG和粪便IgA反应。在经鼻内给予CFA/I加mLT的小鼠中,观察到对ETEC菌株H10407致死性攻击有部分保护作用(P<0.01),并且与对照小鼠相比,CFA/I加mLT免疫小鼠肺部的H10407清除率显著更高(P<0.05)。经鼻内和胃内给予CFA/I和CS6可诱导混合的Th1/Th2免疫反应,以Th2型为主,IgG1>IgG2a可证明这一点。给小鼠给予定植因子,特别是经鼻内途径,可能是在将这些抗原用于志愿者之前测量血清和黏膜对这些抗原免疫反应的有用方法。

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