Evidence map›Paper›PMID 35263761›Full record

ArticleCancer immunology research2022

Phosphoantigen-Stimulated γδ T Cells Suppress Natural Killer-Cell Responses to Missing-Self.

Katherine Walwyn-Brown, Jason Pugh, Alexander T H Cocker, Niassan Beyzaie, Bernhard B Singer, Daniel Olive, Lisbeth A Guethlein, Peter Parham, Zakia Djaoud

Open access · bronzeAbstract readComment
In one paragraph

Article in Cancer immunology research, 2022. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 5 papers.

0numbers the graph read from it
0cells of the map it votes in
5citing papers in PubMed
0.7field-weighted citation impact, top 35% of its field
1 · What the graph read from it

What it found

Each row is one number read from the abstract, on the scale the paper reported it, with its interval. Left of the dashed line favours the treatment, right favours the comparator. Under each row is the sentence it came from. New to these charts? A ten-minute tutorial.

The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.

2 · The registry

The trial behind it

Trials whose registry record cites this paper, or whose number appears in the abstract. A trial that started after this paper was published is citing it as background, not reporting it.

Neither the registry nor the abstract names a trial number. If this is a trial report, that itself is worth knowing.

3 · Its place in the literature

Who cites it

5 citing papers in PubMed, 9 citations in OpenAlex.

  1. γδ T cells and cancer.The Journal of clinical investigation · 2026
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4 · The record

Corrections and comments

5 · Who and what money

Authors and funding

9 authors at 3 institutions in 3 countries.

Katherine Walwyn-BrownDepartment of Structural Biology, Stanford University School of Medicine, Stanford, California.ORCID 0000-0003-2325-5180
Jason PughDepartment of Structural Biology, Stanford University School of Medicine, Stanford, California.
Alexander T H CockerDepartment of Structural Biology, Stanford University School of Medicine, Stanford, California.ORCID 0000-0001-7162-0774
Niassan BeyzaieDepartment of Structural Biology, Stanford University School of Medicine, Stanford, California.ORCID 0000-0002-1910-6919
Bernhard B SingerInstitute of Anatomy, University Hospital, University Duisburg-Essen, Essen, Germany.ORCID 0000-0002-2213-6000
Daniel OliveCRCM, Immunity and Cancer, Inserm, U1068, Institut Paoli-Calmettes, Aix-Marseille Université, UM105, CNRS, UMR7258, Marseille, France.ORCID 0000-0003-1299-4113
Lisbeth A GuethleinDepartment of Structural Biology, Stanford University School of Medicine, Stanford, California.ORCID 0000-0002-1301-8301
Peter ParhamDepartment of Structural Biology, Stanford University School of Medicine, Stanford, California.
Zakia DjaoudDepartment of Structural Biology, Stanford University School of Medicine, Stanford, California.ORCID 0000-0001-9583-8487
Stanford Medicine · USCentre National de la Recherche Scientifique · FRUniversity of Duisburg-Essen · DE

Funding

Functional genetics of human innate immunity in the bimodal gamma delta T cell response to Epstein-Barr Virus and in education of NK cells and their re-education to respond to autologous cellsR01AI136952 · NIAID · STANFORD UNIVERSITY · PI PARHAM, PETER R · 2019 to 2023
$2.0M
Nikon A1Rsi resonant spectral confocal microscopeS10OD010580 · OD · STANFORD UNIVERSITY · PI FULLER, MARGARET T · 2013 to 2013
$377k
NIAID NIH HHS R01 AI136952NIH HHS S10 OD010580
6 · The paper itself

Abstract

γδ T cells stimulated by phosphoantigens (pAg) are potent effectors that secrete Th1 cytokines and kill tumor cells. Consequently, they are considered candidates for use in cancer immunotherapy. However, they have proven only moderately effective in several clinical trials. We studied the consequences of pAg-stimulated γδ T-cell interactions with natural killer (NK) cells and CD8+ T cells, major innate and adaptive effectors, respectively. We found that pAg-stimulated γδ T cells suppressed NK-cell responses to "missing-self" but had no effect on antigen-specific CD8+ T-cell responses. Extensive analysis of the secreted cytokines showed that pAg-stimulated γδ T cells had a proinflammatory profile. CMV-pp65-specific CD8+ T cells primed with pAg-stimulated γδ T cells showed little effect on responses to pp65-loaded target cells. By contrast, NK cells primed similarly with γδ T cells had impaired capacity to degranulate and produce IFNγ in response to HLA class I-deficient targets. This effect depended on BTN3A1 and required direct contact between NK cells and γδ T cells. γδ T-cell priming of NK cells also led to a downregulation of NKG2D and NKp44 on NK cells. Every NK-cell subset was affected by γδ T cell-mediated immunosuppression, but the strongest effect was on KIR+NKG2A- NK cells. We therefore report a previously unknown function for γδ T cells, as brakes of NK-cell responses to "missing-self." This provides a new perspective for optimizing the use of γδ T cells in cancer immunotherapy and for assessing their role in immune responses to pAg-producing pathogens. See related Spotlight by Kabelitz, p. 543.

Indexed as

NeoplasmsReceptors, Antigen, T-Cell, gamma-deltaAntigens, CDButyrophilinsCytokinesHumansKiller Cells, NaturalT-Lymphocytes, CytotoxicAntigens, CDBTN3A1 protein, humanButyrophilinsCytokinesReceptors, Antigen, T-Cell, gamma-delta

Identifiers

PMID35263761
PMCPMC9064994
OpenAlexW4220824364

What OpenQuestion holds

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LicenceTDM
Read underepoch 390

Registered trials

None linked

Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.