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Gut microbial structural variation associates with immune checkpoint inhibitor response

Author

Listed:
  • Rong Liu

    (Central South University
    Hunan Key Laboratory of Pharmacogenetics
    Ministry of Education
    National Clinical Research Center for Geriatric Disorders)

  • You Zou

    (Central South University)

  • Wei-Quan Wang

    (Central South University
    Hunan Key Laboratory of Pharmacogenetics
    Ministry of Education
    National Clinical Research Center for Geriatric Disorders)

  • Jun-Hong Chen

    (Central South University
    Hunan Key Laboratory of Pharmacogenetics
    Ministry of Education
    National Clinical Research Center for Geriatric Disorders)

  • Lei Zhang

    (Central South University
    Hunan Key Laboratory of Pharmacogenetics
    Ministry of Education
    National Clinical Research Center for Geriatric Disorders)

  • Jia Feng

    (Central South University
    Hunan Key Laboratory of Pharmacogenetics
    Ministry of Education
    National Clinical Research Center for Geriatric Disorders)

  • Ji-Ye Yin

    (Central South University
    Hunan Key Laboratory of Pharmacogenetics
    Ministry of Education
    National Clinical Research Center for Geriatric Disorders)

  • Xiao-Yuan Mao

    (Central South University
    Hunan Key Laboratory of Pharmacogenetics
    Ministry of Education
    National Clinical Research Center for Geriatric Disorders)

  • Qing Li

    (Central South University
    Hunan Key Laboratory of Pharmacogenetics
    Ministry of Education
    National Clinical Research Center for Geriatric Disorders)

  • Zhi-Ying Luo

    (Central South University
    Central South University)

  • Wei Zhang

    (Central South University
    Hunan Key Laboratory of Pharmacogenetics
    Ministry of Education
    National Clinical Research Center for Geriatric Disorders)

  • Dao-Ming Wang

    (Department of Genetics
    Department of Pediatrics)

Abstract

The gut microbiota may have an effect on the therapeutic resistance and toxicity of immune checkpoint inhibitors (ICIs). However, the associations between the highly variable genomes of gut bacteria and the effectiveness of ICIs remain unclear, despite the fact that merely a few gene mutations between similar bacterial strains may cause significant phenotypic variations. Here, using datasets from the gut microbiome of 996 patients from seven clinical trials, we systematically identify microbial genomic structural variants (SVs) using SGV-Finder. The associations between SVs and response, progression-free survival, overall survival, and immune-related adverse events are systematically explored by metagenome-wide association analysis and replicated in different cohorts. Associated SVs are located in multiple species, including Akkermansia muciniphila, Dorea formicigenerans, and Bacteroides caccae. We find genes that encode enzymes that participate in glucose metabolism be harbored in these associated regions. This work uncovers a nascent layer of gut microbiome heterogeneity that is correlated with hosts’ prognosis following ICI treatment and represents an advance in our knowledge of the intricate relationships between microbiota and tumor immunotherapy.

Suggested Citation

  • Rong Liu & You Zou & Wei-Quan Wang & Jun-Hong Chen & Lei Zhang & Jia Feng & Ji-Ye Yin & Xiao-Yuan Mao & Qing Li & Zhi-Ying Luo & Wei Zhang & Dao-Ming Wang, 2023. "Gut microbial structural variation associates with immune checkpoint inhibitor response," Nature Communications, Nature, vol. 14(1), pages 1-12, December.
  • Handle: RePEc:nat:natcom:v:14:y:2023:i:1:d:10.1038_s41467-023-42997-7
    DOI: 10.1038/s41467-023-42997-7
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    References listed on IDEAS

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    1. David Zeevi & Tal Korem & Anastasia Godneva & Noam Bar & Alexander Kurilshikov & Maya Lotan-Pompan & Adina Weinberger & Jingyuan Fu & Cisca Wijmenga & Alexandra Zhernakova & Eran Segal, 2019. "Structural variation in the gut microbiome associates with host health," Nature, Nature, vol. 568(7750), pages 43-48, April.
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