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Molecular and Functional Characteristics of a Protective Human Monoclonal Antibody to Serotype 8 Streptococcus pneumoniae Capsular Polysaccharide

机译:血清型8肺炎链球菌荚膜多糖的保护性人类单克隆抗体的分子和功能特征。

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摘要

The structural characteristics and biological activity of human antibodies that are reactive with the capsular polysaccharides of most serotypes of Streptococcus pneumoniae, including serotype 8, are unknown. This paper describes the generation, molecular structure, and protective efficacy of a human monoclonal antibody (MAb) reactive with the capsular polysaccharide of serotype 8 Streptococcus pneumoniae. We generated the immunoglobulin M(κ) [IgM(κ)] MAb D11 by Epstein-Barr virus transformation of peripheral lymphocytes from a Pneumovax recipient. Nucleic acid sequence analysis revealed that MAb D11 uses V3-15/VH3 and A20/Vκ gene segments with evidence of somatic mutation. In vitro studies revealed MAb D11-dependent complement deposition on the capsule of serotype 8 organisms via either the classical or the alternative complement pathway. In vivo, MAb D11 prolonged the survival of both normal and C4-deficient mice with lethal serotype 8 S. pneumoniae infection. Our findings demonstrate that a serotype-specific human IgM with certain structural and functional characteristics was protective in mice lacking a functional classical complement pathway and show that alternative complement pathway activation is an important determinant of pneumococcal protection.
机译:与大多数血清型(包括血清型8)的肺炎链球菌的荚膜多糖有反应性的人抗体的结构特征和生物学活性是未知的。本文描述了与血清型8肺炎链球菌的荚膜多糖反应的人单克隆抗体(MAb)的产生,分子结构和保护功效。我们通过对来自肺炎单胞菌受体的外周淋巴细胞进行爱泼斯坦-巴尔病毒转化,产生了免疫球蛋白M(κ)[IgM(κ)] MAb D11。核酸序列分析表明,单克隆抗体D11使用V3-15 / VH3和A20 /Vκ基因片段,具有体细胞突变的迹象。体外研究表明,通过经典或替代补体途径,MAb D11依赖的补体在血清型8生物的胶囊上沉积。在体内,MAb D11延长了具有致命性血清型8肺炎链球菌感染的正常小鼠和C4缺陷小鼠的存活。我们的研究结果表明,具有某些结构和功能特征的血清型特异性人IgM在缺乏功能性经典补体途径的小鼠中具有保护作用,并显示替代补体途径的激活是肺炎球菌保护的重要决定因素。

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