首页> 外文期刊>Infection and immunity >Murine monoclonal antibodies to Klebsiella pneumoniae protect against lethal endotoxemia and experimental infection with capsulated K. pneumoniae.
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Murine monoclonal antibodies to Klebsiella pneumoniae protect against lethal endotoxemia and experimental infection with capsulated K. pneumoniae.

机译:抗肺炎克雷伯菌的鼠单克隆抗体可预防致命的内毒素血症和被荚膜肺炎克雷伯菌感染的实验性感染。

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To prepare monoclonal antibodies (MAbs) directed against the core-lipid A fractions of smooth lipopoly-saccharide (LPS) from Klebsiella pneumoniae O1:K2, we immunized BALB/c mice with the LPS-associated proteins plus LPS. This preparation exposed the core-lipid A moiety, which is normally hidden in the micellar structure of classical LPS preparations. Among 10 MAbs selected for their reactivity with LPS-associated proteins plus LPS from K. pneumoniae O1:K2, 6 (3A3, 3C2, 3C4, 7D2, 11C3, and 12B6) were directed against the core fraction and 2 (6C5 and 10A5) were directed against the lipid A fraction. Only one (2A4) recognized the O antigen, and one (6D5) had an undefined specificity. When injected before challenge with K. pneumoniae O1:K2 LPS in galactosamine-sensitized mice, five of the MAbs (3C4, 6D5, 7D2, 11C3, and 12B6) provided protection in this model of lethal endotoxemia. MAb 7D2 was also protective in an experimental infection with capsulated K. pneumoniae O1:K2.
机译:要制备针对肺炎克雷伯氏菌O1:K2的平滑脂多糖(LPS)的核心脂质A级分的单克隆抗体(MAb),我们用与LPS相关的蛋白加LPS免疫了BALB / c小鼠。该制剂暴露了核心脂质A部分,其通常隐藏在经典LPS制剂的胶束结构中。在10种与LPS相关蛋白以及肺炎克雷伯菌O1:K2的LPS具有反应性的单克隆抗体中,有6种(3A3、3C2、3C4、7D2、11C3和12B6)针对核心部分,而2种(6C5和10A5)针对脂质A级分。只有一个(2A4)识别O抗原,一个(6D5)具有不确定的特异性。在半乳糖胺致敏的小鼠中,在用肺炎克雷伯菌O1:K2 LPS攻击前注射时,其中5种MAb(3C4、6D5、7D2、11C3和12B6)在这种致命内毒素血症模型中提供了保护。 MAb 7D2在被荚膜肺炎克雷伯菌O1:K2感染的实验性感染中也具有保护作用。

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