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Clostridium difficile flagellin FliC: Evaluation as adjuvant and use in a mucosal vaccine against Clostridium difficile

机译:艰难梭菌鞭毛蛋白FliC:评估为佐剂,并在抗艰难梭菌粘膜疫苗中使用

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摘要

The immunogenicity of bacterial flagellin has been reported in different studies. By its close interaction with the immune system, the flagellin represents an interesting adjuvant and vaccine candidate. Salmonella Typhimurium flagellin has already been tested as adjuvant to stimulate mucosal immunity. Here, we assessed the ability of Clostridium difficile flagellin FliC to act as a mucosal adjuvant, first combined with ovalbumin as antigen and second with a C. difficile surface protein, the precursor of the S-layer proteins SlpA. Using ovalbumin as antigen, we compared the gut mucosal adjuvanticity of FliC to Salmonella Typhimurium flagellin and cholera toxin. Two routes of immunization were tested in a mouse model: intra-rectal and intra-peritoneal, following which, gut mucosal and systemic antibody responses against ovalbumin (Immunoglobulins G and Immunoglobulins A) were analyzed by Enzyme-Linked Immuno Assay in intestinal contents and in sera. In addition, ovalbumin-specific immunoglobulin producing cells were detected in the intestinal lamina propria by Enzyme-Linked Immunospot. Results showed that FliC as adjuvant for immunization targeting ovalbumin was able to stimulate a gut mucosal and systemic antibody response independently of the immunization route. In order to develop a mucosal vaccine to prevent C. difficile intestinal colonization, we assessed in a mouse model the efficacy of FliC as adjuvant compared with cholera toxin co-administrated with the C. difficile S-layer precursor SlpA as antigen. After challenge, a significant decrease of C. difficile intestinal colonization was observed in immunized groups compared to the control group. Our results showed that C. difficile FliC could be used as adjuvant in mucosal vaccination strategy against C. difficile infections.
机译:在不同的研究中已经报道了细菌鞭毛蛋白的免疫原性。通过与免疫系统的紧密相互作用,鞭毛蛋白代表了一种有趣的佐剂和疫苗候选物。鼠伤寒沙门氏菌鞭毛蛋白已被测试为刺激粘膜免疫的佐剂。在这里,我们评估了梭状芽胞杆菌鞭毛蛋白FliC作为粘膜佐剂的能力,首先与卵清蛋白结合作为抗原,其次与艰难梭菌表面蛋白(S层蛋白SlpA的前体)结合。使用卵清蛋白作为抗原,我们比较了FliC与鼠伤寒沙门氏菌鞭毛蛋白和霍乱毒素的肠黏膜黏附性。在小鼠模型中测试了两种免疫途径:直肠内和腹膜内,然后,通过酶联免疫分析法分析了肠内对卵清蛋白的粘膜和全身抗体反应(免疫球蛋白G和免疫球蛋白A)的肠道内容物和血清另外,通过酶联免疫斑点在肠道固有层中检测到卵白蛋白特异性免疫球蛋白产生细胞。结果表明,FliC作为针对卵清蛋白的免疫佐剂能够独立于免疫途径刺激肠道粘膜和全身抗体应答。为了开发一种粘膜疫苗来预防艰难梭菌肠道菌落定植,我们在小鼠模型中评估了FliC作为佐剂的功效,而不是与艰难梭菌S层前体SlpA作为抗原共同施用的霍乱毒素。攻击后,与对照组相比,在免疫组中观察到艰难梭菌肠道定植明显减少。我们的结果表明,艰难梭菌FliC可以作为针对艰难梭菌感染的粘膜疫苗接种策略的佐剂。

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