Wang Qun, Chang Chew-Shun, Pennini Meghan, Pelletier Mark, Rajan Saravanan, Zha Jingying, Chen Yan, Cvitkovic Romana, Sadowska Agnieszka, Heidbrink Thompson Jenny, Yu Lin Hung, Barnes Arnita, Rickert Keith, Wilson Susan, Stover C Kendall, Dall'Acqua William F, Chowdhury Partha S, Xiao Xiaodong
Department of Infectious Disease and Vaccines.
Department of Antibody Discovery and Protein Engineering.
J Infect Dis. 2016 Jun 1;213(11):1800-8. doi: 10.1093/infdis/jiw021. Epub 2016 Jan 14.
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.
目前广泛使用的广谱抗生素对肺炎克雷伯菌感染的治疗效果越来越差,这促使人们探索替代方法,如抗体疗法和/或疫苗,用于预防和治疗。然而,临床菌株谱缺乏经过验证的共同靶点,这构成了重大挑战。我们采用了一种不依赖靶点的方法来鉴定针对肺炎克雷伯菌的保护性抗体。通过对调理吞噬杀伤活性进行功能筛选,从噬菌体展示和杂交瘤平台中分离出几种单克隆抗体。我们进一步确定它们的共同靶抗原是MrkA,它是III型菌毛复合物中的一种主要蛋白质,并表明这些不依赖血清型的抗MrkA抗体在体外可减少生物膜形成,并在多种小鼠肺炎模型中提供保护。重要的是,用纯化的MrkA蛋白免疫的小鼠在受到肺炎克雷伯菌攻击后,细菌载量也有所降低。综上所述,这些结果支持MrkA作为肺炎克雷伯菌抗体治疗和疫苗的一个有前景的靶点。