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针对个别伯氏疏螺旋体分离株或其重组外膜蛋白A(OspA)的免疫血清可保护重症联合免疫缺陷(SCID)小鼠免受同源菌株的感染,但对不同OspA/OspB基因型的菌株只能提供部分保护或完全没有保护作用。

Immune sera to individual Borrelia burgdorferi isolates or recombinant OspA thereof protect SCID mice against infection with homologous strains but only partially or not at all against those of different OspA/OspB genotype.

作者信息

Schaible U E, Wallich R, Kramer M D, Gern L, Anderson J F, Museteanu C, Simon M M

机构信息

Max-Planck-Institut für Immunbiologie, Freiburg, Germany.

出版信息

Vaccine. 1993;11(10):1049-54. doi: 10.1016/0264-410x(93)90132-h.

Abstract

The outer surface proteins OspA and OspB of Borrelia burgdorferi have recently been demonstrated to be major target proteins for protective antibodies in mice against infection with the homologous spirochaetal strain. However, it has become clear from a variety of studies that B. burgdorferi isolates of different geographical origin and/or sources are heterogeneous and that they can be divided into at least six subgroups according to their distinct OspA/OspB genotypes. In order to analyse cross-protection between these subgroups we have now generated immune sera to various isolates of B. burgdorferi with different OspA/OspB genotypes. We show that passive immunization with antisera specific for whole spirochaetes or recombinant OspA of one spirochaetal isolate protects severe combined immunodeficiency mice against infection with strains of the corresponding OspA/OspB genotype but only partially or not at all against infection with isolates expressing distinct OspA/OspB genotypes. The incomplete protection mediated by individual antisera against independent isolates of B. burgdorferi suggests that an effective subunit vaccine against Lyme disease should consist of a mixture of OspA structures covering the heterogeneity of this protein within the species B. burgdorferi.

摘要

最近已证明,伯氏疏螺旋体的外表面蛋白OspA和OspB是小鼠体内针对同源螺旋体菌株感染的保护性抗体的主要靶蛋白。然而,从各种研究中已清楚地看到,不同地理来源和/或来源的伯氏疏螺旋体分离株具有异质性,并且根据其不同的OspA/OspB基因型可将它们分为至少六个亚组。为了分析这些亚组之间的交叉保护作用,我们现在已针对具有不同OspA/OspB基因型的各种伯氏疏螺旋体分离株制备了免疫血清。我们发现,用针对一种螺旋体分离株的全螺旋体或重组OspA的特异性抗血清进行被动免疫,可保护严重联合免疫缺陷小鼠免受相应OspA/OspB基因型菌株的感染,但对表达不同OspA/OspB基因型的分离株感染仅提供部分保护或完全没有保护作用。单个抗血清对伯氏疏螺旋体独立分离株介导的不完全保护表明,一种有效的莱姆病亚单位疫苗应包含覆盖伯氏疏螺旋体物种内该蛋白异质性的OspA结构混合物。

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