Evidence map›Paper›PMID 41960781›Full record

ArticleeLife2026

Contrasting roles for IKK-regulated inflammatory signalling pathways for development and maintenance of type 1 and adaptive γδ T cells.

Farjana Islam, Cayman Williams, Thea Hogan, Louise V Webb, Ines Boal-Carvalho, Benedict Seddon

Abstract read
In one paragraph

Article in eLife, 2026. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.

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

0 citing papers in PubMed.

No citing paper in PubMed yet.

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.

Farjana IslamInstitute of Immunity and Transplantation, Division of Infection and Immunity, University College London, London, United Kingdom.ORCID https://orcid.org/0000-0001-8274-2021
Cayman WilliamsInstitute of Immunity and Transplantation, Division of Infection and Immunity, University College London, London, United Kingdom.
Thea HoganInstitute of Immunity and Transplantation, Division of Infection and Immunity, University College London, London, United Kingdom.
Louise V WebbInstitute of Immunity and Transplantation, Division of Infection and Immunity, University College London, London, United Kingdom.ORCID https://orcid.org/0009-0000-8862-0199
Ines Boal-CarvalhoInstitute of Immunity and Transplantation, Division of Infection and Immunity, University College London, London, United Kingdom.
Benedict SeddonInstitute of Immunity and Transplantation, Division of Infection and Immunity, University College London, London, United Kingdom.ORCID https://orcid.org/0000-0003-4352-3373

Funding

Medical Research Council MR/P011225/1
6 · The paper itself

Abstract

The inhibitor of kappa-B kinase (IKK) complex is a critical regulator of cell death and inflammatory signalling in multiple cell types. Phosphorylation of IκB proteins by IKK results in their degradation and consequent activation of NF-κB transcription factors. RIPK1, a critical cell death regulator, is also a direct target of IKK kinase activity, thereby repressing its cell death activity. In αβ T cells, the RIPK1 kinase activity of IKK is critical for normal thymic development while mature αβ T cells require IKK for both activation of NF-κB dependent survival programmes and repression of RIPK1. γδ T cells play a unique and versatile role in host immunity with specific effector functions that enable them to act as early responders in immune defence. The role of IKK-regulated pathways in their development and survival is not known. Here, we dissect the function of IKK and downstream pathways for normal γδ T cell homeostasis. We find that IKK is critical to establish replete γδ T cell populations, but that mechanism varys between different subsets. Type 1 γδ T cells require IKK-dependent NF-κB activation for their generation, while IKK is redundant for development of adaptive γδ T cells. Instead, IKK-dependent NF-κB activation is required for their long-term survival. We also find evidence that IKK repression of RIPK1 is required for survival of peripheral but not thymic γδ T cells. Ablation of CASPASE8 did not rescue γδ T cells in the absence of IKK but rather revealed a potent sensitivity of all γδ subsets to necroptosis, which was rescued by kinase-dead RIPK1. Overall, we reveal critical requirements for IKK-regulated inflammatory pathways by γδ T cells that contrast with those of αβ T cells, and between different subsets, highlighting the complexity of the regulation of these pathways in the adaptive immune system.

Indexed as

I-kappa B KinaseInflammationReceptors, Antigen, T-Cell, gamma-deltaSignal TransductionT-LymphocytesAnimalsMiceNF-kappa BReceptor-Interacting Protein Serine-Threonine KinasesI-kappa B KinaseNF-kappa BReceptor-Interacting Protein Serine-Threonine KinasesReceptors, Antigen, T-Cell, gamma-deltaRipk1 protein, mouseapoptosisimmunologyinflammationmousenecroptosisNF kappa B

Identifiers

PMID41960781
PMCPMC13068431

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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.