Evidence map›Paper›PMID 32647184›Full record

ArticleNature communications2020

Th1 responses in vivo require cell-specific provision of OX40L dictated by environmental cues.

Dominika W Gajdasik, Fabrina Gaspal, Emily E Halford, Remi Fiancette, Emma E Dutton, Claire Willis, Timo Rückert, Chiara Romagnani, Audrey Gerard, Sarah L Bevington and 4 more

Open access · goldAbstract read
In one paragraph

Article in Nature communications, 2020. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 16 papers.

0numbers the graph read from it
0cells of the map it votes in
16citing papers in PubMed
2.0field-weighted citation impact, top 12% 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

16 citing papers in PubMed, 39 citations in OpenAlex.

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  15. OX40L-OX40 Signaling in Atopic Dermatitis.Journal of clinical medicine · 2021
    Article
  16. 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

14 authors at 6 institutions in 2 countries.

Dominika W GajdasikInstitute of Immunology and Immunotherapy, College of Medical and Dental Sciences, University of Birmingham, Birmingham, UK.
Fabrina GaspalInstitute of Immunology and Immunotherapy, College of Medical and Dental Sciences, University of Birmingham, Birmingham, UK.
Emily E HalfordInstitute of Immunology and Immunotherapy, College of Medical and Dental Sciences, University of Birmingham, Birmingham, UK.ORCID http://orcid.org/0000-0003-1347-2683
Remi FiancetteInstitute of Immunology and Immunotherapy, College of Medical and Dental Sciences, University of Birmingham, Birmingham, UK.
Emma E DuttonInstitute of Immunology and Immunotherapy, College of Medical and Dental Sciences, University of Birmingham, Birmingham, UK.
Claire WillisInstitute of Immunology and Immunotherapy, College of Medical and Dental Sciences, University of Birmingham, Birmingham, UK.
Timo RückertMed. Klinik m.S. Gastroenterologie, Infektiologie und Rheumatologie and Deutsches Rheuma-Forschungszentrum, Charité - Universitätsmedizin Berlin, Berlin, Germany.ORCID http://orcid.org/0000-0003-1433-1372
Chiara RomagnaniMed. Klinik m.S. Gastroenterologie, Infektiologie und Rheumatologie and Deutsches Rheuma-Forschungszentrum, Charité - Universitätsmedizin Berlin, Berlin, Germany.ORCID http://orcid.org/0000-0002-5167-7463
Audrey GerardThe Kennedy Institute of Rheumatology, The University of Oxford, Oxford, UK.ORCID http://orcid.org/0000-0003-3059-3065
Sarah L BevingtonInstitute of Cancer and Genomic Sciences, College of Medical and Dental Sciences, University of Birmingham, Birmingham, UK.
Andrew S MacDonaldManchester Collaborative Centre for Inflammation Research, Faculty of Biology, Medicine and Health, University of Manchester, Manchester, UK.ORCID http://orcid.org/0000-0002-5356-1149
Marina BottoDepartment of Medicine, Centre for Inflammatory Disease, Imperial College London, London, UK.ORCID http://orcid.org/0000-0002-1458-3791
Timothy VyseDivision of Medical and Molecular Genetics and Immunology, Infection and Inflammatory Disease, King's College London, London, UK.ORCID http://orcid.org/0000-0003-1123-1464
David R WithersInstitute of Immunology and Immunotherapy, College of Medical and Dental Sciences, University of Birmingham, Birmingham, UK. d.withers@bham.ac.uk.ORCID http://orcid.org/0000-0003-3757-7594
University of Birmingham · GBGerman Rheumatism Research Centre · DEImperial College London · GBKing's College London · GBUniversity of Manchester · GBUniversity of Oxford · GB

Funding

Wellcome TrustWellcome Trust 110199/Z/15/Z
6 · The paper itself

Abstract

The OX40-OX40L pathway provides crucial co-stimulatory signals for CD4 T cell responses, however the precise cellular interactions critical for OX40L provision in vivo and when these occur, remains unclear. Here, we demonstrate that provision of OX40L by dendritic cells (DCs), but not T cells, B cells nor group 3 innate lymphoid cells (ILC3s), is critical specifically for the effector Th1 response to an acute systemic infection with Listeria monocytogenes (Lm). OX40L expression by DCs is regulated by cross-talk with NK cells, with IFNγ signalling to the DC to enhance OX40L in a mechanism conserved in both mouse and human DCs. Strikingly, DC expression of OX40L is redundant in a chronic intestinal Th1 response and expression by ILC3s is necessary. Collectively these data reveal tissue specific compartmentalisation of the cellular provision of OX40L and define a mechanism controlling DC expression of OX40L in vivo.

Indexed as

Cellular MicroenvironmentAnimalsCell CommunicationCuesDendritic CellsHumansInterferon-gammaInterleukin-12IntestinesKi-1 AntigenKiller Cells, NaturalListeria monocytogenesMice, Inbred C57BLOX40 LigandReceptors, CXCR5Receptors, OX40CXCR5 protein, mouseInterferon-gammaInterleukin-12Ki-1 AntigenOX40 LigandReceptors, CXCR5Receptors, OX40

Identifiers

PMID32647184
PMCPMC7347572
OpenAlexW3041557856

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.