| Literature DB >> 26768253 |
Qun Wang1, Chew-Shun Chang2, Meghan Pennini1, Mark Pelletier1, Saravanan Rajan2, Jingying Zha1, Yan Chen2, Romana Cvitkovic1, Agnieszka Sadowska1, Jenny Heidbrink Thompson3, Hung Yu Lin3, Arnita Barnes2, Keith Rickert2, Susan Wilson2, C Kendall Stover1, William F Dall'Acqua2, Partha S Chowdhury2, Xiaodong Xiao2.
Abstract
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.Entities:
Keywords: Klebsiella pneumoniae; MrkA; biofilm; functional screening; hybridoma; monoclonal antibodies; opsonophagocytic killing (OPK); organ burden; phage display; vaccine
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Year: 2016 PMID: 26768253 DOI: 10.1093/infdis/jiw021
Source DB: PubMed Journal: J Infect Dis ISSN: 0022-1899 Impact factor: 5.226