金黄色葡萄球菌
单克隆抗体
微生物学
抗生素
生物
毒素
抗体
体内
单克隆
病菌
免疫系统
体外
葡萄球菌感染
病毒学
免疫学
细菌
生物化学
生物技术
遗传学
作者
Wei-Tong Hou,Chen-Rui Shen,Peng Ji,Liwen Jiang,Shiyu Guo,Xi-Ran Qiu,Yu Zhang,Hui Shen,Yuanying Jiang,Mao‐Mao An
标识
DOI:10.1093/infdis/jiad215
摘要
Abstract Staphylococcus aureus is a major human pathogen associated with high mortality rates. The extensive use of antibiotics is associated with the rise of drug resistance, and exotoxins are not targeted by antibiotics. Therefore, monoclonal antibody (mAb) therapy has emerged as a promising solution to solve the clinical problems caused by refractory S aureus. Recent research suggests that the synergistic effects of several cytotoxins, including bicomponent toxins, are critical to the pathogenesis of S aureus. By comparing the amino acid sequences, researchers found that α-toxin and bicomponent toxins have high homology. Therefore, we aimed to screen an antibody, designated an all-in-one mAb, that could neutralize α-toxin and bicomponent toxins through hybridoma fusion. We found that this mAb has a significant pharmacodynamic effect within in vivo mouse models and in vitro experiments.
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