Szijártó Valéria, Guachalla Luis M, Visram Zehra C, Hartl Katharina, Varga Cecília, Mirkina Irina, Zmajkovic Jakub, Badarau Adriana, Zauner Gerhild, Pleban Clara, Magyarics Zoltán, Nagy Eszter, Nagy Gábor
Arsanis Biosciences GmbH, Vienna, Austria.
Arsanis Biosciences GmbH, Vienna, Austria
Antimicrob Agents Chemother. 2015;59(6):3109-16. doi: 10.1128/AAC.04494-14. Epub 2015 Mar 16.
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.
大肠杆菌序列型131(ST131)-O25b:H4克隆已在全球传播,并导致相当一部分多重耐药性肠外感染。我们制备了针对该菌系中保守的脂多糖O25b抗原的人源化单克隆抗体(MAb)。这些MAb可结合活细菌细胞表面,而与所表达的荚膜类型无关。在体外血清杀菌试验中,以人血清作为补体来源时,MAb可诱导>95%的细菌杀伤。在小鼠菌血症模型中观察到低剂量抗体的保护效果。通过使用保护性MAb的无糖基化衍生物研究其体内作用方式。在使用在人血清中生长的细菌以模拟相关临床情况的试验中,证实了与活大肠杆菌细胞的显著结合以及体外和体内疗效。鉴于针对多重耐药革兰氏阴性病原体的新型抗生素研发进展缓慢,用杀菌性抗体进行被动免疫为控制由大肠杆菌ST131-O25b:H4引起的感染提供了一种治疗选择。