Evidence map›Paper›PMID 41709661›Full record

ArticleEuropean journal of immunology2026

IL-21 Selectively Augments Cytotoxic Potential of Antigen-Activated MAIT Cells.

Laura E Wedlock, Rajesh Lamichhane, Meg C Webley, Selena C L Gilmer, Andrea J Vernall, James E Ussher

Abstract read
In one paragraph

Article in European journal of immunology, 2026. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 2 papers.

0numbers the graph read from it
0cells of the map it votes in
2citing 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

2 citing papers in PubMed.

  1. Review
  2. Article
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.

Laura E WedlockDepartment of Microbiology and Immunology, University of Otago, Dunedin, New Zealand.
Rajesh LamichhaneDepartment of Microbiology and Immunology, University of Otago, Dunedin, New Zealand.
Meg C WebleyDepartment of Microbiology and Immunology, University of Otago, Dunedin, New Zealand.
Selena C L GilmerDepartment of Chemistry, University of Otago, Dunedin, New Zealand.
Andrea J VernallDepartment of Chemistry, University of Otago, Dunedin, New Zealand.
James E UssherDepartment of Microbiology and Immunology, University of Otago, Dunedin, New Zealand.ORCID 0000-0001-9222-7680

Funding

Health Research Council of New Zealand 19/457The Dunedin Basic Medical Sciences Course Trust Professor Sandy Smith Memorial Scholarship (L.E.W.)
6 · The paper itself

Abstract

Mucosal-associated invariant T (MAIT) cells are unconventional cytotoxic T cells restricted by MHC class 1 related molecule, MR1. They are activated through their T cell receptor (TCR) by derivatives from microbial riboflavin synthesis or independently of TCR signalling via IL-12 and IL-18. Upon activation, MAIT cells upregulate cytotoxic molecules granzyme B and perforin and lyse bacterially-infected cells. While cytokines act as co-stimulatory molecules that enhance MAIT cell activation, their specific role in regulating MAIT cell cytotoxicity remains unresolved. We show that the cytokine IL-21 enhances expression of granzyme B and perforin on TCR or IL-12/IL-18-activated MAIT cells but has a limited effect on MAIT cell cytokine production. Using a flow cytometry-based cytotoxic assay, we show priming MAIT cells with IL-21 enhances their ability to kill 5-OP-RU-treated B cell lines. We demonstrate a previously unexplored co-stimulatory role for IL-21 that selectively augments the cytotoxic potential of MAIT cells.

Indexed as

Cytotoxicity, ImmunologicInterleukinsLymphocyte ActivationMucosal-Associated Invariant T CellsAnimalsB-LymphocytesGranzymesHistocompatibility Antigens Class IHumansInterleukin-12Interleukin-18Interleukin-21Minor Histocompatibility AntigensPerforinReceptors, Antigen, T-CellGranzymesHistocompatibility Antigens Class IInterleukin-12Interleukin-18Interleukin-21InterleukinsMinor Histocompatibility AntigensMR1 protein, humanPerforinReceptors, Antigen, T-Cellco‐stimulationcytotoxicityIL‐21mucosal‐associated invariant T cellsTCR activation

Identifiers

PMID41709661
PMCPMC12917470

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Registered trials

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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.