首页> 美国卫生研究院文献>Infection and Immunity >Protection of C3H/HeN mice from challenge with Borrelia burgdorferi through active immunization with OspA OspB or OspC but not with OspD or the 83-kilodalton antigen.
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Protection of C3H/HeN mice from challenge with Borrelia burgdorferi through active immunization with OspA OspB or OspC but not with OspD or the 83-kilodalton antigen.

机译:通过用OspAOspB或OspC主动免疫(但不是用OspD或83-千达尔顿抗原)主动免疫保护C3H / HeN小鼠免受伯氏疏螺旋体攻击。

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摘要

Recent advances in the development of animal models for Lyme borreliosis have provided means of identifying potential targets for the design of a subunit vaccine to prevent this disease. The C3H/HeN mouse model was used to study several Borrelia burgdorferi antigens from a single isolate for their ability to elicit borreliacidal and protective antibodies. The ospA, ospB, ospC, ospD, and 83-kDa genes from a California isolate, SON 188, were cloned and expressed in Escherichia coli as proteins fused to the C-terminal end of maltose-binding protein. Active immunization of mice with these fusion proteins elicited high titers of antibodies that recognized the homologous SON 188 antigens upon immunoblotting. Antibodies generated to the OspA and OspB fusion proteins, but not to the OspC, OspD, and the 83-kDa fusion proteins, demonstrated in vitro borreliacidal activity. Challenge of all actively immunized mice with 10(7) SON 188 spirochetes resulted in infection in all mice receiving the OspD or 83-kDa immunogens but not in any mice receiving the OspA, OspB, or OspC fusion proteins. These results demonstrate the potential of OspA, OspB, and OspC as components of a subunit vaccine for the prevention of Lyme borreliosis.
机译:莱姆病(Lyme borreliosis)莱姆病的动物模型开发的最新进展提供了识别设计亚单位疫苗以预防这种疾病的潜在目标的手段。 C3H / HeN小鼠模型用于研究单个分离物中的几种疏螺旋体抗原,它们具有引发疏螺旋体酸性和保护性抗体的能力。将来自加利福尼亚分离株SON 188的ospA,ospB,ospC,ospD和83-kDa基因克隆并在大肠杆菌中表达为与麦芽糖结合蛋白C端融合的蛋白。用这些融合蛋白对小鼠进行主动免疫可产生高滴度的抗体,该抗体在免疫印迹后即可识别同源的SON 188抗原。对OspA和OspB融合蛋白产生的抗体,但对OspC,OspD和83-kDa融合蛋白却没有,它们在体外具有硼酸的活性。用10(7)SON 188螺旋体攻击所有主动免疫的小鼠会导致感染OspD或83-kDa免疫原的所有小鼠感染,但未感染OspA,OspB或OspC融合蛋白的任何小鼠感染。这些结果证明,OspA,OspB和OspC作为亚单位疫苗的成分可预防莱姆病。

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