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Distinct gene expression signatures comparing latent tuberculosis infection with different routes of Bacillus Calmette-Guérin vaccination

Author

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  • Richard F. Silver

    (Case Western Reserve University School of Medicine
    The Louis Stokes Cleveland Department of Veterans’ Affairs Medical Center)

  • Mei Xia

    (Saint Louis University School of Medicine
    Saint Louis University School of Medicine)

  • Chad E. Storer

    (Washington University School of Medicine)

  • Jessica R. Jarvela

    (Case Western Reserve University School of Medicine
    The Louis Stokes Cleveland Department of Veterans’ Affairs Medical Center)

  • Michelle C. Moyer

    (Case Western Reserve University School of Medicine
    The Louis Stokes Cleveland Department of Veterans’ Affairs Medical Center)

  • Azra Blazevic

    (Saint Louis University School of Medicine
    Saint Louis University School of Medicine)

  • David A. Stoeckel

    (Saint Louis University School of Medicine)

  • Erin K. Rakey

    (Saint Louis University School of Medicine)

  • Jan M. Tennant

    (Saint Louis University School of Medicine)

  • Johannes B. Goll

    (Emmes Corporation)

  • Richard D. Head

    (Washington University School of Medicine)

  • Daniel F. Hoft

    (Saint Louis University School of Medicine
    Saint Louis University School of Medicine
    Department of Molecular Microbiology & Immunology Saint Louis University School of Medicine)

Abstract

Tuberculosis remains an international health threat partly because of limited protection from pulmonary tuberculosis provided by standard intradermal vaccination with Bacillus of Calmette and Guérin (BCG); this may reflect the inability of intradermal vaccination to optimally induce pulmonary immunity. In contrast, respiratory Mycobacterium tuberculosis infection usually results in the immune-mediated bacillary containment of latent tuberculosis infection (LTBI). Here we present RNA-Seq-based assessments of systemic and pulmonary immune cells from LTBI participants and recipients of intradermal and oral BCG. LTBI individuals uniquely display ongoing immune activation and robust CD4 T cell recall responses in blood and lung. Intradermal BCG is associated with robust systemic immunity but only limited pulmonary immunity. Conversely, oral BCG induces limited systemic immunity but distinct pulmonary responses including enhanced inflammasome activation potentially associated with mucosal-associated invariant T cells. Further, IL-9 is identified as a component of systemic immunity in LTBI and intradermal BCG, and pulmonary immunity following oral BCG.

Suggested Citation

  • Richard F. Silver & Mei Xia & Chad E. Storer & Jessica R. Jarvela & Michelle C. Moyer & Azra Blazevic & David A. Stoeckel & Erin K. Rakey & Jan M. Tennant & Johannes B. Goll & Richard D. Head & Daniel, 2023. "Distinct gene expression signatures comparing latent tuberculosis infection with different routes of Bacillus Calmette-Guérin vaccination," Nature Communications, Nature, vol. 14(1), pages 1-17, December.
  • Handle: RePEc:nat:natcom:v:14:y:2023:i:1:d:10.1038_s41467-023-44136-8
    DOI: 10.1038/s41467-023-44136-8
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    References listed on IDEAS

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    1. Patricia A. Darrah & Joseph J. Zeppa & Pauline Maiello & Joshua A. Hackney & Marc H. Wadsworth & Travis K. Hughes & Supriya Pokkali & Phillip A. Swanson & Nicole L. Grant & Mark A. Rodgers & Megha Kam, 2020. "Prevention of tuberculosis in macaques after intravenous BCG immunization," Nature, Nature, vol. 577(7788), pages 95-102, January.
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