肺炎克雷伯菌
单克隆抗体
微生物学
抗体
生物
伞
病毒学
肺炎克雷伯菌
抗原
肺炎
抗生素
大肠杆菌
免疫学
细菌
医学
金黄色葡萄球菌
基因
内科学
生物化学
遗传学
作者
Qun Wang,Chew-shun Chang,Meghan E. Pennini,Mark Pelletier,Saravanan Rajan,Jingying Zha,Yan Chen,Romana Cvitkovic,Agnieszka Sadowska,Jenny Heidbrink Thompson,Hung Yu Lin,Arnita Barnes,Keith Rickert,Susan Wilson,C. Kendall Stover,William F. Dall’Acqua,Partha S. Chowdhury,Xiaodong Xiao
标识
DOI:10.1093/infdis/jiw021
摘要
The increasing incidence of Klebsiella pneumoniae infections refractory to treatment with current broad-spectrum antibiotic classes warrants the exploration of alternative approaches, such as antibody therapy and/or vaccines, for prevention and treatment. However, the lack of validated targets shared by spectrums of clinical strains poses a significant challenge. We adopted a target-agnostic approach to identify protective antibodies against K. pneumoniae Several monoclonal antibodies were isolated from phage display and hybridoma platforms by functional screening for opsonophagocytic killing activity. We further identified their common target antigen to be MrkA, a major protein in the type III fimbriae complex, and showed that these serotype-independent anti-MrkA antibodies reduced biofilm formation in vitro and conferred protection in multiple murine pneumonia models. Importantly, mice immunized with purified MrkA proteins also showed reduced bacterial burden following K. pneumoniae challenge. Taken together, these results support MrkA as a promising target for K. pneumoniae antibody therapeutics and vaccines.
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