メインナビゲーションにスキップ 検索にスキップ メインコンテンツにスキップ

A feasibility study for personalized phage therapy against drug-resistant bacteria in Japan

  • Kayoko Hayakawa
  • , Kotaro Kiga
  • , Shinjiro Ojima
  • , Kotaro Chihara
  • , Azumi Tamura
  • , Wakana Yamashita
  • , Tomohiro Nakamura
  • , Aa Haeruman Azam
  • , Wenhan Nie
  • , Yuta Sato
  • , Jun Sakai
  • , Kohei Kondo
  • , Yoshimasa Takahashi
  • , Koichi Watashi
  • , Sho Saito
  • , Yuki Moriyama
  • , Masami Kurokawa
  • , Kazuhisa Mezaki
  • , Hirotake Ohashi
  • , Yasukata Ohashi
  • Takahiro Nishimura, Koh Shinohara, Yoshiaki Yamagishi, Yohei Doi, Norio Ohmagari

研究成果: ジャーナルへの寄稿学術論文査読

抄録

Introduction: Personalized phage therapy is used in Europe and the United States to treat intractable infections caused by drug-resistant bacteria. This pilot study aimed to acquire feasibility data for clinical trials of individualized phage therapy in Japan. Methods: An observational study was conducted from August 2023 to September 2024 in adults with drug-resistant bacterial infections and treatment failure or recurrence/relapse following antimicrobial therapy. Phages with activity against the detected bacteria were then identified from the environment and an existing phage library. Results: Thirty patients with drug-resistant bacterial infections were enrolled. Of these, six (20 %) died within 30 days of detection. The most commonly detected bacteria were methicillin-resistant Staphylococcus aureus (MRSA) (n = 10, 33.3 %) and carbapenem-resistant Pseudomonas aeruginosa (CRPA) (n = 5, 16.7 %). The most common nontuberculous mycobacterium (NTM) was Mycobacterium avium (n = 4, 13.3 %), followed by Mycobacterium abscessus (n = 2, 6.7 %). In terms of infection types, respiratory tract infections were the most common (n = 13, 43.3 %), followed by bone and joint infections (n = 6, 20 %) and skin and soft tissue infections (n = 6, 20 %). Phages with a titer of 108 PFU/ml or higher could be prepared for 26 out of 30 strains (86.7 %). Phages against CRPA were more readily identified from the environment than for MRSA and NTM. A phage against CRPA was purified to a lipopolysaccharide concentration of 0.023 EU/108 PFU. Conclusion: Personalized phages can be prepared for intractable infections caused by drug-resistant bacteria. These results support the conduct of clinical trials to implement personalized phage therapy in Japan.

本文言語英語
論文番号102770
ジャーナルJournal of Infection and Chemotherapy
31
9
DOI
出版ステータス出版済み - 09-2025
外部発表はい

UN SDG

この成果は、次の持続可能な開発目標に貢献しています

  1. SDG 3 - すべての人に健康と福祉を
    SDG 3 すべての人に健康と福祉を

All Science Journal Classification (ASJC) codes

  • 微生物学(医療)
  • 薬理学(医学)
  • 感染症

フィンガープリント

「A feasibility study for personalized phage therapy against drug-resistant bacteria in Japan」の研究トピックを掘り下げます。これらがまとまってユニークなフィンガープリントを構成します。

引用スタイル