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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

机译:使用肠毒素致病性大肠杆菌定殖因子CFA / I和CS6联合和不联合突变型不耐热肠毒素给予BALB / c小鼠的粘膜免疫

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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.
机译:分别给小鼠(BALB / c)鼻内(IN)和胃内(IG)施用ETEC定植因子(CF),CFA / I和CS6,并添加和不添加R192G突变体不耐热肠毒素(mLT),并测量免疫原性和功效。小鼠IN注射CFA / I诱导强烈的血清和粪便IgG和IgA反应。 IG对小鼠的CFA / I IG诱导可诱导血清IgG和粪便IgA反应,但仅当mLT与CFA / I共同给药时,才检测到血清IgA滴度。对小鼠进行CS6的IN诱导可诱导血清IgG抗体,而与CS6共同给药时,mLT可增强血清IgG反应。仅当mLT与CS6共同使用时,才检测到血清和粪便IgA反应。 IG给予CS6加mLT诱导血清IgG和粪便IgA反应。在接受CFA / I + mLT免疫的小鼠中,对ETEC菌株H10407的致死性攻击具有部分保护作用(P <0.01),并且从CFA / I + mLT免疫小鼠的肺中清除H10407的速率明显高于来自对照小鼠(P <0.05)。 CFA / I和CS6分别在IN和IG上诱导混合的Th1 / Th2免疫应答,其中以IgG1> IgG2a为主的Th2型为主。尤其是通过IN途径向小鼠施用定居因子,可能会成为一种有用的方法,用于在志愿者使用这些抗原之前测量对这些抗原的血清和粘膜免疫应答。

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