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首页> 外文期刊>Infection and immunity >Protection against Experimental Helicobacter pylori Infection after Immunization with Inactivated H. pylori Whole-Cell Vaccines
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Protection against Experimental Helicobacter pylori Infection after Immunization with Inactivated H. pylori Whole-Cell Vaccines

机译:灭活幽门螺杆菌全细胞疫苗免疫后预防实验性幽门螺杆菌感染

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摘要

The protective effect of therapeutic oral immunization with homologous and heterologous formalin-inactivated Helicobacter pylori cells given together with cholera toxin as an adjuvant was evaluated with C57BL/6 mice infected with H. pylori Sydney strain 1 (SS1). The bacteria used for immunization were strains that were either homologous or heterologous with regard to the O antigen (i.e., the Lewis antigen [Le antigen]) expressed by the lipopolysaccharide of the infecting H. pylori SS1 strain. We found that repeated oral immunization with inactivated H. pylori SS1 cells can significantly inhibit an existing infection (P < 0.001) and that the protection induced by such therapeutic immunization extends to protection against reinfection (P < 0.001). A similar level of protection was also achieved by immunization with another inactivated H. pylori strain having the same O antigen (Le antigen) as the infecting H. pylori SS1 strain. In contrast, immunization with inactivated strains expressing a heterologous O antigen, Lex, provided less protection or no protection. Immunization with H. pylori lysate preparations, on the other hand, resulted in significant comparable protection whether the lysates were prepared from an Lex strain or an Ley strain. Postimmunization gastritis was seen in mice that were protected after vaccination but not in unimmunized or unprotected mice. In conclusion, therapeutic immunization with inactivated H. pylori whole-cell vaccines may provide strong protection both against experimental H. pylori infection and against later reinfection.
机译:用感染了 H的C57BL / 6小鼠评估了同种和异种福尔马林灭活的幽门螺杆菌细胞与霍乱毒素作为佐剂的口服治疗性免疫保护作用。幽门螺杆菌悉尼菌株1(SS1)。用于免疫的细菌是与感染H的脂多糖表达的O抗原(即Lewis抗原[Le抗原])同源或异源的菌株。幽门螺杆菌SS1菌株。我们发现用灭活的 H反复进行口服免疫。 pylori SS1细胞可以显着抑制现有感染( P <0.001),并且这种治疗性免疫所诱导的保护作用可以扩展为防止再感染( P <0.001) )。通过用另一种灭活的 H免疫也获得了相似的保护水平。具有与感染 H相同的O抗原(Le抗原)的幽门螺杆菌菌株。幽门螺杆菌SS1菌株。相比之下,用表达异源O抗原的灭活菌株Le x 进行的免疫接种提供的保护较少或没有保护。用 H免疫。另一方面,无论是从Le x 菌株还是Le y 菌株制备的幽门螺杆菌裂解物制剂,都可得到相当可比的保护。在接种疫苗后受到保护的小鼠中观察到免疫后胃炎,但在未免疫或未保护的小鼠中未见。总之,用灭活的 H进行治疗性免疫。幽门螺杆菌全细胞疫苗可提供针对实验性H的强大保护。幽门螺杆菌感染和以后的再感染。

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