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<p>Pertussis, also known as whooping cough, is a highly infectious respiratory disease caused by the bacterium <i>Bordetella pertussis</i>. The bacterial virulence factor, pertussis toxin (PT), is associated with the manifestation of the characteristic symptoms of pertussis and the severe form of this disease. Increasing case numbers and the lack of treatment options highlight the need to develop novel pharmacological strategies, e.g., the generation of specific PT inhibitors. Recently, we identified the endogenous human protein α<sub>1</sub>-antitrypsin (α<sub>1</sub>AT) as an inhibitor of PT from a screening of a human hemofiltrate protein/peptide library. In the present work, we tested an in-house α<sub>1</sub>AT peptide bank to identify an α<sub>1</sub>AT region with anti-PT activity. Then, we compared the sequences of the positive hits from the peptide bank with all known α<sub>1</sub>AT fragments in the hemofiltrate samples to find new active peptides. In total, 36 peptides were tested for their PT inhibition, leading to the identification of an endogenous α<sub>1</sub>AT fragment, α<sub>1</sub>AT HF, derived from hemofiltrate with anti-PT activity. This peptide had no toxic effects on HeLa cells and in vivo on zebrafish embryos, rendering it an attractive lead compound for further evaluation to treat pertussis in the future.</p>

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An endogenous human peptide derived from α1-antitrypsin as a novel pharmacological inhibitor of Bordetella pertussis toxin

  • 期刊论文

  • 出版模式：

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  • 发表日期：

    2025年11月17日

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  • Stefanie Lietz,
  • Lena-Marie Sokolowski,
  • Alexander Beyschlag,
  • Helena Rosenau,
  • Annika Siewert,
  • Armando A. Rodríguez Alfonso,
  • Nico Preising,
  • Ludger Ständker,
  • Sebastian Wiese,
  • Janet Köhler,
  • Gilbert Weidinger,
  • Jan Münch,
  • Arto T. Pulliainen,
  • Katharina Ernst,
  • Holger Barth

摘要

Pertussis, also known as whooping cough, is a highly infectious respiratory disease caused by the bacterium Bordetella pertussis. The bacterial virulence factor, pertussis toxin (PT), is associated with the manifestation of the characteristic symptoms of pertussis and the severe form of this disease. Increasing case numbers and the lack of treatment options highlight the need to develop novel pharmacological strategies, e.g., the generation of specific PT inhibitors. Recently, we identified the endogenous human protein α1-antitrypsin (α1AT) as an inhibitor of PT from a screening of a human hemofiltrate protein/peptide library. In the present work, we tested an in-house α1AT peptide bank to identify an α1AT region with anti-PT activity. Then, we compared the sequences of the positive hits from the peptide bank with all known α1AT fragments in the hemofiltrate samples to find new active peptides. In total, 36 peptides were tested for their PT inhibition, leading to the identification of an endogenous α1AT fragment, α1AT HF, derived from hemofiltrate with anti-PT activity. This peptide had no toxic effects on HeLa cells and in vivo on zebrafish embryos, rendering it an attractive lead compound for further evaluation to treat pertussis in the future.