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Modulation of lytic molecules restrain serial killing in γδ T lymphocytes
KTH, School of Engineering Sciences (SCI), Applied Physics, Biophysics. KTH, Centres, Science for Life Laboratory, SciLifeLab.ORCID iD: 0000-0002-8379-7267
Department of Medicine Huddinge, Karolinska Institutet, Karolinska University Hospital, Stockholm, Sweden.
Precision Immunotherapy Alliance, University of Oslo, Oslo, Norway; Department of Cancer Immunology, Institute for Cancer Research, Oslo University Hospital, Oslo, Norway.
KTH, School of Engineering Sciences (SCI), Applied Physics. KTH, Centres, Science for Life Laboratory, SciLifeLab.
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Number of Authors: 172023 (English)In: Nature Communications, E-ISSN 2041-1723, Vol. 14, no 1, article id 6035Article in journal (Refereed) Published
Abstract [en]

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.

Place, publisher, year, edition, pages
Springer Nature , 2023. Vol. 14, no 1, article id 6035
National Category
Cell and Molecular Biology Cancer and Oncology
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URN: urn:nbn:se:kth:diva-338405DOI: 10.1038/s41467-023-41634-7ISI: 001095471200022PubMedID: 37758698Scopus ID: 2-s2.0-85172238386OAI: oai:DiVA.org:kth-338405DiVA, id: diva2:1806693
Note

QC 20231123

Available from: 2023-10-23 Created: 2023-10-23 Last updated: 2023-12-04Bibliographically approved

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Sandoz, PatrickThunberg, SaraErikson, ElinaSandström, NiklasVerron, QuentinÖnfelt, Björn

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