Evidence map›Paper›PMID 32486268›Full record

ReviewInternational journal of molecular sciences2020

License to Kill: When iNKT Cells Are Granted the Use of Lethal Cytotoxicity.

Angélica Díaz-Basabe, Francesco Strati, Federica Facciotti

Abstract readReview
In one paragraph

Review in International journal of molecular sciences, 2020. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 29 papers.

0numbers the graph read from it
0cells of the map it votes in
29citing papers in PubMed
–field-weighted citation impact
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

29 citing papers in PubMed.

  1. Review
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  9. American journal of cancer research · 2024
    Review
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  12. Article
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  15. Article
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  18. Article
  19. Review
  20. Advances in NK cell production.Cellular & molecular immunology · 2022
    Review
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

3 authors.

Angélica Díaz-BasabeDepartment of Experimental Oncology, IEO European Institute of Oncology IRCCS, 20139 Milan, Italy.ORCID 0000-0003-2096-1223
Francesco StratiDepartment of Experimental Oncology, IEO European Institute of Oncology IRCCS, 20139 Milan, Italy.ORCID 0000-0001-7217-3355
Federica FacciottiDepartment of Experimental Oncology, IEO European Institute of Oncology IRCCS, 20139 Milan, Italy.ORCID 0000-0002-2541-9428

Funding

Associazione Italiana per la Ricerca sul Cancro IG2019-22923
6 · The paper itself

Abstract

Invariant Natural Killer T (iNKT) cells are a non-conventional, innate-like, T cell population that recognize lipid antigens presented by the cluster of differentiation (CD)1d molecule. Although iNKT cells are mostly known for mediating several immune responses due to their massive and diverse cytokine release, these cells also work as effectors in various contexts thanks to their cytotoxic potential. In this Review, we focused on iNKT cell cytotoxicity; we provide an overview of iNKT cell subsets, their activation cues, the mechanisms of iNKT cell cytotoxicity, the specific roles and outcomes of this activity in various contexts, and how iNKT killing functions are currently activated in cancer immunotherapies. Finally, we discuss the future perspectives for the better understanding and potential uses of iNKT cell killing functions in tumor immunosurveillance.

Indexed as

Immunity, InnateAnimalsAntigen-Presenting CellsAntigens, CD1dHumansHypoxiaImmune SystemImmunotherapyLipidsLymphocyte ActivationMonitoring, ImmunologicNatural Killer T-CellsNeoplasmsPrognosisAntigens, CD1dCD1D protein, humanLipidscancerCD1dcytotoxicityinfectionsiNKT

Identifiers

PMID32486268
PMCPMC7312231

What OpenQuestion holds

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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.