Evidence map›Paper›PMID 38855101›Full record

ArticleFrontiers in immunology2024

Interleukin-1 regulates follicular T cells during the germinal center reaction.

Aude Belbezier, Paul Engeroff, Gwladys Fourcade, Hélène Vantomme, Romain Vaineau, Bruno Gouritin, Bertrand Bellier, Isabelle Brocheriou, Nicolas Tchitchek, Stephanie Graff-Dubois and 1 more

Abstract read
In one paragraph

Article in Frontiers in immunology, 2024. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 11 papers.

0numbers the graph read from it
0cells of the map it votes in
11citing 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

11 citing papers in PubMed.

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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

11 authors.

Aude BelbezierSorbonne Université, INSERM, Immunology-Immunopathology-Immunotherapy (i3), Paris, France.
Paul EngeroffSorbonne Université, INSERM, Immunology-Immunopathology-Immunotherapy (i3), Paris, France.
Gwladys FourcadeSorbonne Université, INSERM, Immunology-Immunopathology-Immunotherapy (i3), Paris, France.
Hélène VantommeSorbonne Université, INSERM, Immunology-Immunopathology-Immunotherapy (i3), Paris, France.
Romain VaineauSorbonne Université, INSERM, Immunology-Immunopathology-Immunotherapy (i3), Paris, France.
Bruno GouritinSorbonne Université, INSERM, Immunology-Immunopathology-Immunotherapy (i3), Paris, France.
Bertrand BellierSorbonne Université, INSERM, Immunology-Immunopathology-Immunotherapy (i3), Paris, France.
Isabelle BrocheriouAssistance Publique - Hôpitaux de Pari (AP-HP), Hôpital Pitié-Salpêtrière, Department of Pathology, Paris, France.
Nicolas TchitchekSorbonne Université, INSERM, Immunology-Immunopathology-Immunotherapy (i3), Paris, France.
Stephanie Graff-DuboisSorbonne Université, INSERM, Immunology-Immunopathology-Immunotherapy (i3), Paris, France.
David KlatzmannSorbonne Université, INSERM, Immunology-Immunopathology-Immunotherapy (i3), Paris, France.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Introduction: Antibody production and the generation of memory B cells are regulated by T follicular helper (Tfh) and T follicular regulatory (Tfr) cells in germinal centers. However, the precise role of Tfr cells in controlling antibody production is still unclear. We have previously shown that both Tfh and Tfr cells express the IL-1R1 agonist receptor, whereas only Tfr cells express the IL-1R2 decoy and IL-1Ra antagonist receptors. We aimed to investigate the role of IL-1 receptors in the regulation of B cell responses by Tfh and Tfr. Methods: We generated mice with IL-1 receptors inactivated in Tfh or Tfr and measured antibody production and cell activation after immunisation. Results: While IL-1β levels are increased in the draining lymph node after immunisation, antigen-specific antibody levels and cell phenotypes indicated that IL-1β can activate both Tfh and Tfr cells through IL-1R1 stimulation. Surprisingly, expression of IL-1R2 and IL-1Ra on Tfr cells does not block IL-1 activation of Tfh cells, but rather prevents IL-1/IL-1R1-mediated early activation of Tfr cells. IL-1Rs also regulate the antibody response to autoantigens and its associated pathophysiology in an experimental lupus model. Discussion: Collectively, our results show that IL-1 inhibitory receptors expressed by Tfr cells prevent their own activation and suppressive function, thus licensing IL-1-mediated activation of Tfh cells after immunisation. Further mechanistic studies should unravel these complex interactions between IL-1β and follicular helper and regulatory T cells and provide new avenues for therapeutic intervention.

Indexed as

Germinal CenterT Follicular Helper CellsT-Lymphocytes, RegulatoryAnimalsAntibody FormationB-LymphocytesInterleukin-1Interleukin-1betaLymphocyte ActivationMiceMice, Inbred C57BLReceptors, Interleukin-1Receptors, Interleukin-1 Type IIL1R1 protein, mouseInterleukin-1Interleukin-1betaReceptors, Interleukin-1Receptors, Interleukin-1 Type Iadaptive immunityautoimmune diseaseshumoral responseimmunotherapyvaccination

Identifiers

PMID38855101
PMCPMC11157057

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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.