Evidence map›Paper›PMID 34298791›Full record

ReviewCancers2021

Regulation and Functions of Protumoral Unconventional T Cells in Solid Tumors.

Emilie Barsac, Carolina de Amat Herbozo, Loïc Gonzalez, Thomas Baranek, Thierry Mallevaey, Christophe Paget

Open access · goldAbstract readReview
In one paragraph

Review in Cancers, 2021. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 7 papers.

0numbers the graph read from it
0cells of the map it votes in
7citing papers in PubMed
0.4field-weighted citation impact, top 43% 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

7 citing papers in PubMed, 7 citations in OpenAlex.

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4 · The record

Corrections and comments

PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.

5 · Who and what money

Authors and funding

6 authors at 2 institutions in 2 countries.

Emilie BarsacCentre d'Étude des Pathologies Respiratoires, UMR1100, INSERM (Institut National de la Santé et de la Recherche Médicale), Faculté de Médecine, Université de Tours, 37012 Tours, France.
Carolina de Amat HerbozoDepartment of Immunology, University of Toronto, Toronto, ON M5S 1A8, Canada.
Loïc GonzalezCentre d'Étude des Pathologies Respiratoires, UMR1100, INSERM (Institut National de la Santé et de la Recherche Médicale), Faculté de Médecine, Université de Tours, 37012 Tours, France.
Thomas BaranekCentre d'Étude des Pathologies Respiratoires, UMR1100, INSERM (Institut National de la Santé et de la Recherche Médicale), Faculté de Médecine, Université de Tours, 37012 Tours, France.
Thierry MallevaeyDepartment of Immunology, University of Toronto, Toronto, ON M5S 1A8, Canada.
Christophe PagetCentre d'Étude des Pathologies Respiratoires, UMR1100, INSERM (Institut National de la Santé et de la Recherche Médicale), Faculté de Médecine, Université de Tours, 37012 Tours, France.ORCID 0000-0002-5374-5407
Université de Tours · FRUniversity of Toronto · CA

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

The vast majority of studies on T cell biology in tumor immunity have focused on peptide-reactive conventional T cells that are restricted to polymorphic major histocompatibility complex molecules. However, emerging evidence indicated that unconventional T cells, including γδ T cells, natural killer T (NKT) cells and mucosal-associated invariant T (MAIT) cells are also involved in tumor immunity. Unconventional T cells span the innate-adaptive continuum and possess the unique ability to rapidly react to nonpeptide antigens via their conserved T cell receptors (TCRs) and/or to activating cytokines to orchestrate many aspects of the immune response. Since unconventional T cell lineages comprise discrete functional subsets, they can mediate both anti- and protumoral activities. Here, we review the current understanding of the functions and regulatory mechanisms of protumoral unconventional T cell subsets in the tumor environment. We also discuss the therapeutic potential of these deleterious subsets in solid cancers and why further feasibility studies are warranted.

Indexed as

cytokinesimmunoregulationMAITNKTprotumorsolid cancertumor microenvironmentunconventional T cellsγδT

Identifiers

PMID34298791
PMCPMC8304984
OpenAlexW3184307285

What OpenQuestion holds

Textmetadata
LicenceCC BY
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.