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Antibody WN1 222-5 mimics Toll-like receptor 4 binding in the recognition of LPS

机译:抗体WN1 222-5在识别LPS时模仿Toll样受体4结合

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摘要

Escherichia coli infections, a leading cause of septic shock, remain a major threat to human health because of the fatal action to endotoxin (LPS). Therapeutic attempts to neutralize endotoxin currently focus on inhibiting the interaction of the toxic component lipid A with myeloid differentiating factor 2, which forms a trimeric complex together with Toll-like receptor 4 to induce immune cell activation. The 1.73-Å resolution structure of the unique endotoxin-neutralizing protective antibody WN1 222-5 in complex with the core region shows that it recognizes LPS of all E. coli serovars in a manner similar to Toll-like receptor 4, revealing that protection can be achieved by targeting the inner core of LPS and that recognition of lipid A is not required. Such interference with Toll-like receptor complex formation opens new paths for antibody sepsis therapy independent of lipid A antagonists.
机译:大肠杆菌感染是败血性休克的主要原因,由于对内毒素(LPS)的致命作用,仍然是人类健康的主要威胁。中和内毒素的治疗尝试目前集中于抑制毒性成分脂质A与髓样分化因子2的相互作用,后者与Toll样受体4一起形成三聚体复合物以诱导免疫细胞活化。独特的内毒素中和性保护性抗体WN1 222-5与核心区域复合的1.73-Å分辨率结构表明,它以类似于Toll样受体4的方式识别所有大肠杆菌血清型的LPS,表明该保护作用可以通过靶向LPS的内芯可以达到目的,而无需识别脂质A。这种对Toll样受体复合物形成的干扰为抗体败血症治疗开辟了新途径,而独立于脂质A拮抗剂。

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