广泛中和抗毒素B单克隆抗体AZD5148在不同和全球当代艰难梭菌分离株中的表位保守性

Kelly Ann Mahool,Emily Nguyen,Victoria Godfrey,Ann Marie Stanley,Tyler Brady,Adam Gamson,Kim Rosenthal,Justin Green,Ondrej Podlaha,Bret Sellman,Christine Tkaczyk,Vancheswaran Gopalakrishnan
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引用次数: 0

摘要

BACKGROUNDC。艰难梭菌毒素B是艰难梭菌感染(CDI)的毒力因子,是临床验证的预防CDI复发的靶点。AZD5148是一种毒素B中和的人单克隆抗体,与毒素B葡萄糖基转移酶结构域的表位结合。在此,我们的目标是利用从公共存储库获得的9,134个全球艰难梭菌基因组来评估该结合表位的保守性,以确认对中和至关重要的残基是保守的。方法对2015-2023年两个独立来源的分离株进行变异召唤、序列分型和系统发育分析。我们用两种不同的细胞系测试了AZD5148对细胞毒性的体外中和作用。结果AZD5148表位在所有地理区域和序列类型(STs)中都高度保守,其结合位点的平均保守频率(99.58%)高于bezlotoxumab(82.47%)。AZD5148在体外对8种最近循环的核糖型也表现出广泛的中和作用。结论AZD5148表位具有高度保守性,因此不太可能受到近期流行的艰难梭菌核型和STs中大多数基因型变异的影响。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Epitope conservation of AZD5148, a broadly neutralizing anti-Toxin B monoclonal antibody, among diverse and global contemporary Clostridioides difficile isolates.
BACKGROUND C. difficile Toxin B is a virulence factor for C. difficile infections (CDI), and a clinically validated target for prevention of CDI recurrence. AZD5148 is a Toxin B neutralizing human monoclonal antibody that binds to an epitope on the Toxin B glucosyltransferase domain. Herein, we aim to evaluate the conservation of this binding epitope using a collection of 9,134 global C. difficile genomes obtained from a public repository to confirm that residues that are crucial for neutralization are conserved. METHODS Using isolates collected between 2015-2023 from two independent sources, we performed variant calling, sequence typing and phylogenetic analysis. We tested in vitro neutralization of cytotoxicity by AZD5148 using two different cell-lines. RESULTS Herein, we showed that the AZD5148 epitope is highly conserved across all geographic regions and sequence types (STs) and has a higher average conservation frequency in its binding site (99.58%) when compared to bezlotoxumab (82.47%). AZD5148 also exhibited broad neutralization in vitro against 8 recently circulating ribotypes. CONCLUSIONS Our comprehensive analysis of global sequences found the AZD5148 epitope to be highly conserved, and thus unlikely to be impacted by most of the genotypic variations in recently circulating C. difficile ribotypes and STs.
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