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Characterization of a Protective Monoclonal Antibody Recognizing Staphylococcus aureus MSCRAMM Protein Clumping Factor A

机译:保护性单克隆抗体的表征 识别金黄色葡萄球菌MSCRAMM蛋白 聚集因子 一个

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摘要

The Staphylococcus aureus MSCRAMM (microbial surface components recognizing adhesive matrix molecules) protein clumping factor A (ClfA) has been shown to be a critical virulence factor in several experimental models of infection. This report describes the generation, characterization, and in vivo evaluation of a murine monoclonal antibody (MAb) against ClfA. Flow cytometric analysis revealed that MAb 12-9 recognized ClfA protein expressed by all of the clinical S. aureus strains obtained from a variety of sources. In assays measuring whole-cell S. aureus binding to human fibrinogen, MAb 12-9 inhibited S. aureus binding by over 90% and displaced up to 35% of the previously adherent S. aureus bacteria. Furthermore, a single infusion of MAb 12-9 was protective against an intravenous challenge with a methicillin-resistant strain of S. aureus in a murine sepsis model (P < 0.0001). These data suggest that anti-ClfA MAb 12-9 should be further investigated as a novel immunotherapy for the treatment and prevention of life-threatening S. aureus infections.
机译:在几种感染实验模型中,金黄色葡萄球菌MSCRAMM(识别粘附基质分子的微生物表面成分)蛋白聚集因子A(ClfA)已被证明是一种关键的致病因子。该报告描述了针对ClfA的鼠类单克隆抗体(MAb)的产生,表征和体内评估。流式细胞仪分析显示,MAb 12-9识别从各种来源获得的所有临床金黄色葡萄球菌菌株表达的ClfA蛋白。在测量全细胞金黄色葡萄球菌与人纤维蛋白原结合的测定中,MAb 12-9抑制金黄色葡萄球菌结合超过90%,并置换了多达35%的先前粘附的金黄色葡萄球菌细菌。此外,在鼠败血症模型中,单次输注单抗12-9可以抵抗耐甲氧西林金黄色葡萄球菌对金黄色葡萄球菌的静脉内攻击(P <0.0001)。这些数据表明抗ClfA MAb 12-9应该是 进一步研究了其作为一种新型的免疫疗法,用于治疗和 预防威胁生命的金黄色葡萄球菌 感染。

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