Evidence map›Paper›PMID 34885076›Full record

ReviewCancers2021

Immune Checkpoints and Innate Lymphoid Cells-New Avenues for Cancer Immunotherapy.

Nicolas Jacquelot, Maryam Ghaedi, Kathrin Warner, Douglas C Chung, Sarah Q Crome, Pamela S Ohashi

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 15 papers.

0numbers the graph read from it
0cells of the map it votes in
15citing papers in PubMed
1.2field-weighted citation impact, top 21% 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

15 citing papers in PubMed, 17 citations in OpenAlex.

  1. Review
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  10. Programmed cell death-1 receptor-mediated regulation of TbetProceedings of the National Academy of Sciences of the United States of America · 2023
    Article
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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 1 institution in 1 country.

Nicolas JacquelotPrincess Margaret Cancer Centre, University Health Network, Toronto, ON M5G 2M9, Canada.ORCID 0000-0003-0282-1892
Maryam GhaediPrincess Margaret Cancer Centre, University Health Network, Toronto, ON M5G 2M9, Canada.
Kathrin WarnerPrincess Margaret Cancer Centre, University Health Network, Toronto, ON M5G 2M9, Canada.
Douglas C ChungPrincess Margaret Cancer Centre, University Health Network, Toronto, ON M5G 2M9, Canada.
Sarah Q CromeDepartment of Immunology, University of Toronto, Toronto, ON M5S 1A8, Canada.
Pamela S OhashiPrincess Margaret Cancer Centre, University Health Network, Toronto, ON M5G 2M9, Canada.
University Health Network · CA

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Immune checkpoints (IC) are broadly characterized as inhibitory pathways that tightly regulate the activation of the immune system. These molecular "brakes" are centrally involved in the maintenance of immune self-tolerance and represent a key mechanism in avoiding autoimmunity and tissue destruction. Antibody-based therapies target these inhibitory molecules on T cells to improve their cytotoxic function, with unprecedented clinical efficacies for a number of malignancies. Many of these ICs are also expressed on innate lymphoid cells (ILC), drawing interest from the field to understand their function, impact for anti-tumor immunity and potential for immunotherapy. In this review, we highlight ILC specificities at different tissue sites and their migration potential upon inflammatory challenge. We further summarize the current understanding of IC molecules on ILC and discuss potential strategies for ILC modulation as part of a greater anti-cancer armamentarium.

Indexed as

cancerimmune checkpointsimmune regulationimmunotherapyinnate lymphoid cellsmigrationnatural killer cellstissue homeostasistrafficking

Identifiers

PMID34885076
PMCPMC8657134
OpenAlexW3215570798

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.