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单克隆抗体可抵御泛耐药肺炎克雷伯菌。

Monoclonal antibodies protect against pandrug-resistant Klebsiella pneumoniae.

作者信息

Roscioli Emanuele, Zucconi Galli Fonseca Vittoria, Bosch Soraya Soledad, Paciello Ida, Maccari Giuseppe, Cardinali Giulia, Batani Giampiero, Stazzoni Samuele, Tiseo Giusy, Giordano Cesira, Yuwei Shen, Capoccia Laura, Cardamone Dario, Ridelfi Matteo, Troisi Marco, Manganaro Noemi, Mugnaini Chiara, De Santi Concetta, Ciabattini Annalisa, Cerofolini Linda, Fragai Marco, Licastro Danilo, Wyres Kelly, Dortet Laurent, Barnini Simona, Nicolau David P, Menichetti Francesco, Falcone Marco, Abdelraouf Kamilia, Sala Claudia, Kabanova Anna, Rappuoli Rino

机构信息

Monoclonal Antibody Discovery (MAD) Lab, Fondazione Toscana Life Sciences, Siena, Italy.

Department of Biotechnology, Chemistry and Pharmacy, University of Siena, Siena, Italy.

出版信息

Nature. 2025 Oct 1. doi: 10.1038/s41586-025-09391-3.

Abstract

The 'silent pandemic' caused by antimicrobial resistance requires innovative therapeutic approaches. Human monoclonal antibodies (mAbs), which are among the most transformative and safe drugs in oncology and autoimmunity, are rarely used for infectious diseases and not yet used for antimicrobial resistance. Here we applied an antigen-agnostic strategy to isolate extremely potent human mAbs against Klebsiella pneumoniae sequence type 147 (ST147), a hypervirulent and pandrug-resistant lineage that is spreading globally. Isolated mAbs target the KL64 capsule and the O-antigen. However, although mAbs displayed bactericidal activity in the picomolar range in vitro, only the capsule-specific mAbs were protective against fulminant bloodstream infection by ST147 and two geographically and genetically distant carbapenem-resistant KL64-bearing K. pneumoniae. Protection observed in vivo correlated with in vitro bacterial uptake by macrophages and enchained bacterial growth. Our study thus describes a mAb that protects against pandrug-resistant K. pneumoniae and provides a strategy to isolate mAbs and identify mAbs that confer protection against bacteria with antimicrobial resistance.

摘要

由抗菌药物耐药性引发的“无声大流行”需要创新的治疗方法。人单克隆抗体(mAb)是肿瘤学和自身免疫领域最具变革性和安全性的药物之一,却很少用于传染病治疗,尚未应用于抗菌药物耐药性的治疗。在此,我们应用一种不依赖抗原的策略,分离出针对肺炎克雷伯菌序列型147(ST147)的超强效人单克隆抗体,ST147是一种高毒力且对多种药物耐药的菌系,正在全球范围内传播。分离出的单克隆抗体靶向KL64荚膜和O抗原。然而,尽管单克隆抗体在体外皮摩尔范围内显示出杀菌活性,但只有荚膜特异性单克隆抗体对ST147以及两种地理和基因上相距遥远的耐碳青霉烯类、携带KL64的肺炎克雷伯菌引起的暴发性血流感染具有保护作用。体内观察到的保护作用与巨噬细胞对细菌的体外摄取以及细菌生长的连锁反应相关。因此,我们的研究描述了一种可抵御对多种药物耐药的肺炎克雷伯菌的单克隆抗体,并提供了一种分离单克隆抗体以及鉴定可抵御具有抗菌药物耐药性细菌的单克隆抗体的策略。

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