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Human antibodies targeting a Mycobacterium transporter protein mediate protection against tuberculosis

Author

Listed:
  • Avia Watson

    (Tel Aviv University)

  • Hao Li

    (Tsinghua University School of Medicine
    China Agricultural University)

  • Bingting Ma

    (Tsinghua University School of Medicine)

  • Ronen Weiss

    (Tel Aviv University)

  • Daniele Bendayan

    (Shmuel Harofe Hospital)

  • Lilach Abramovitz

    (Tel Aviv University)

  • Noam Ben-Shalom

    (Tel Aviv University)

  • Michael Mor

    (Tel Aviv University)

  • Erica Pinko

    (Shmuel Harofe Hospital)

  • Michal Bar Oz

    (The Hebrew University of Jerusalem)

  • Zhenqi Wang

    (Tsinghua University School of Medicine)

  • Fengjiao Du

    (Beijing Chest Hospital, Capital Medical University)

  • Yu Lu

    (Beijing Chest Hospital, Capital Medical University)

  • Jan Rybniker

    (Department of Internal Medicine, Division of Infectious Diseases, University of Cologne
    German Center for Infection Research (DZIF))

  • Rony Dahan

    (Weizmann Institute of Science)

  • Hairong Huang

    (Capital Medical University, Beijing Tuberculosis and Thoracic Tumor Institute)

  • Daniel Barkan

    (The Hebrew University of Jerusalem)

  • Ye Xiang

    (Tsinghua University School of Medicine)

  • Babak Javid

    (Tsinghua University School of Medicine
    University of California)

  • Natalia T. Freund

    (Tel Aviv University)

Abstract

Mycobacterium tuberculosis (Mtb) exposure drives antibody responses, but whether patients with active tuberculosis elicit protective antibodies, and against which antigens, is still unclear. Here we generate monoclonal antibodies from memory B cells of one patient to investigate the B cell responses during active infection. The antibodies, members of four distinct B cell clones, are directed against the Mtb phosphate transporter subunit PstS1. Antibodies p4-36 and p4-163 reduce Mycobacterium bovis-BCG and Mtb levels in an ex vivo human whole blood growth inhibition assay in an FcR-dependent manner; meanwhile, germline versions of p4-36 and p4-163 do not bind Mtb. Crystal structures of p4-36 and p4-170, complexed to PstS1, are determined at 2.1 Å and 2.4 Å resolution, respectively, to reveal two distinctive PstS1 epitopes. Lastly, a prophylactic p4-36 and p4-163 treatment in Mtb-infected Balb/c mice reduces bacterial lung burden by 50%. Our study shows that inhibitory anti-PstS1 B cell responses arise during active tuberculosis.

Suggested Citation

  • Avia Watson & Hao Li & Bingting Ma & Ronen Weiss & Daniele Bendayan & Lilach Abramovitz & Noam Ben-Shalom & Michael Mor & Erica Pinko & Michal Bar Oz & Zhenqi Wang & Fengjiao Du & Yu Lu & Jan Rybniker, 2021. "Human antibodies targeting a Mycobacterium transporter protein mediate protection against tuberculosis," Nature Communications, Nature, vol. 12(1), pages 1-11, December.
  • Handle: RePEc:nat:natcom:v:12:y:2021:i:1:d:10.1038_s41467-021-20930-0
    DOI: 10.1038/s41467-021-20930-0
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