<p>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<sup><CitationRef CitationID="CR1">1</CitationRef></sup> and autoimmunity<sup><CitationRef CitationID="CR2">2</CitationRef></sup>, are rarely used for infectious diseases and not yet used for antimicrobial resistance<sup><CitationRef CitationID="CR3">3</CitationRef></sup>. Here we applied an antigen-agnostic strategy to isolate extremely potent human mAbs against <i>Klebsiella pneumoniae</i> 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 <i>K. pneumoniae</i>. 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 <i>K. pneumoniae</i> and provides a strategy to isolate mAbs and identify mAbs that confer protection against bacteria with antimicrobial resistance.</p>

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Monoclonal antibodies protect against pandrug-resistant Klebsiella pneumoniae

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

摘要

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 oncology1 and autoimmunity2, are rarely used for infectious diseases and not yet used for antimicrobial resistance3. 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.