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Modulation of lytic molecules restrain serial killing in γδ T lymphocytes

Author

Listed:
  • Patrick A. Sandoz

    (KTH Royal Institute of Technology)

  • Kyra Kuhnigk

    (Karolinska Institutet, Karolinska University Hospital)

  • Edina K. Szabo

    (University of Oslo
    Oslo University Hospital)

  • Sarah Thunberg

    (KTH Royal Institute of Technology)

  • Elina Erikson

    (KTH Royal Institute of Technology)

  • Niklas Sandström

    (KTH Royal Institute of Technology)

  • Quentin Verron

    (KTH Royal Institute of Technology)

  • Andreas Brech

    (University of Oslo
    University of Oslo
    Oslo University)

  • Carsten Watzl

    (TU Dortmund)

  • Arnika K. Wagner

    (Karolinska Institutet, Karolinska University Hospital)

  • Evren Alici

    (Karolinska Institutet, Karolinska University Hospital)

  • Karl-Johan Malmberg

    (Karolinska Institutet, Karolinska University Hospital
    University of Oslo
    Oslo University Hospital)

  • Michael Uhlin

    (Karolinska Institutet
    Karolinska University Hospital)

  • Björn Önfelt

    (KTH Royal Institute of Technology
    Karolinska Institutet, Karolinska University Hospital
    Karolinska Institutet)

Abstract

γδ T cells play a pivotal role in protection against various types of infections and tumours, from early childhood on and throughout life. They consist of several subsets characterised by adaptive and innate-like functions, with Vγ9Vδ2 being the largest subset in human peripheral blood. Although these cells show signs of cytotoxicity, their modus operandi remains poorly understood. Here we explore, using live single-cell imaging, the cytotoxic functions of γδ T cells upon interactions with tumour target cells with high temporal and spatial resolution. While γδ T cell killing is dominated by degranulation, the availability of lytic molecules appears tightly regulated in time and space. In particular, the limited co-occurrence of granzyme B and perforin restrains serial killing of tumour cells by γδ T cells. Thus, our data provide new insights into the cytotoxic arsenal and functions of γδ T cells, which may guide the development of more efficient γδ T cell based adoptive immunotherapies.

Suggested Citation

  • Patrick A. Sandoz & Kyra Kuhnigk & Edina K. Szabo & Sarah Thunberg & Elina Erikson & Niklas Sandström & Quentin Verron & Andreas Brech & Carsten Watzl & Arnika K. Wagner & Evren Alici & Karl-Johan Mal, 2023. "Modulation of lytic molecules restrain serial killing in γδ T lymphocytes," Nature Communications, Nature, vol. 14(1), pages 1-16, December.
  • Handle: RePEc:nat:natcom:v:14:y:2023:i:1:d:10.1038_s41467-023-41634-7
    DOI: 10.1038/s41467-023-41634-7
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