| Literature DB >> 25779571 |
Valéria Szijártó1, Luis M Guachalla1, Zehra C Visram1, Katharina Hartl1, Cecília Varga1, Irina Mirkina1, Jakub Zmajkovic1, Adriana Badarau1, Gerhild Zauner1, Clara Pleban1, Zoltán Magyarics1, Eszter Nagy1, Gábor Nagy2.
Abstract
The Escherichia coli sequence type 131 (ST131)-O25b:H4 clone has spread worldwide and become responsible for a significant proportion of multidrug-resistant extraintestinal infections. We generated humanized monoclonal antibodies (MAbs) that target the lipopolysaccharide O25b antigen conserved within this lineage. These MAbs bound to the surface of live bacterial cells irrespective of the capsular type expressed. In a serum bactericidal assay in vitro, MAbs induced >95% bacterial killing in the presence of human serum as the complement source. Protective efficacy at low antibody doses was observed in a murine model of bacteremia. The mode of action in vivo was investigated by using aglycosylated derivatives of the protective MAbs. The significant binding to live E. coli cells and the in vitro and in vivo efficacy were corroborated in assays using bacteria grown in human serum to mimic relevant clinical conditions. Given the dry pipeline of novel antibiotics against multidrug-resistant Gram-negative pathogens, passive immunization with bactericidal antibodies offers a therapeutic alternative to control infections caused by E. coli ST131-O25b:H4.Entities:
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Year: 2015 PMID: 25779571 PMCID: PMC4432214 DOI: 10.1128/AAC.04494-14
Source DB: PubMed Journal: Antimicrob Agents Chemother ISSN: 0066-4804 Impact factor: 5.191