Evidence map›Paper›PMID 32161355›Full record

ArticleMucosal immunology2021

αvβ8 integrin-expression by BATF3-dependent dendritic cells facilitates early IgA responses to Rotavirus.

J Nakawesi, S This, J Hütter, M Boucard-Jourdin, V Barateau, K Getachew Muleta, L J Gooday, K Fog Thomsen, A Garcias López, I Ulmert and 7 more

Open access · hybridAbstract read
PubMed Publisher
In one paragraph

Article in Mucosal immunology, 2021. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 28 papers.

0numbers the graph read from it
0cells of the map it votes in
28citing papers in PubMed
1.9field-weighted citation impact, top 14% 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

28 citing papers in PubMed, 43 citations in OpenAlex.

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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

17 authors at 7 institutions in 5 countries.

J Nakawesi *Immunology Section, Lund University, 221 48, Lund, Sweden.
S This *CIRI, Centre International de Recherche en Infectiologie, Univ Lyon, Inserm, U1111, Université Claude Bernard Lyon 1, CNRS, UMR5308, ENS de Lyon, F-69007, Lyon, France.
J HütterDivision of Biopharma, Institute for Health Technology, Technical University of Denmark (DTU), 2800, Kongens Lyngby, Denmark.
M Boucard-JourdinCIRI, Centre International de Recherche en Infectiologie, Univ Lyon, Inserm, U1111, Université Claude Bernard Lyon 1, CNRS, UMR5308, ENS de Lyon, F-69007, Lyon, France.
V BarateauCIRI, Centre International de Recherche en Infectiologie, Univ Lyon, Inserm, U1111, Université Claude Bernard Lyon 1, CNRS, UMR5308, ENS de Lyon, F-69007, Lyon, France.
K Getachew MuletaImmunology Section, Lund University, 221 48, Lund, Sweden.
L J GoodayImmunology Section, Lund University, 221 48, Lund, Sweden.
K Fog ThomsenDivision of Biopharma, Institute for Health Technology, Technical University of Denmark (DTU), 2800, Kongens Lyngby, Denmark.
A Garcias LópezDivision of Biopharma, Institute for Health Technology, Technical University of Denmark (DTU), 2800, Kongens Lyngby, Denmark.
I UlmertDivision of Biopharma, Institute for Health Technology, Technical University of Denmark (DTU), 2800, Kongens Lyngby, Denmark.
D PoncetInstitute for Integrative Biology of the Cell (I2BC), CEA, CNRS, Université Paris-Sud, INRA, Université Paris-Saclay, Gif-sur-Yvette Cedex, France.
B MalissenCentre d'Immunologie de Marseille-Luminy, Aix Marseille Université, INSERM, CNRS UMR, Marseille 13288, France; Centre d'Immunophénomique, Aix Marseille Université, INSERM, CNRS, Marseille, 13288, France.
H GreenbergDepartments of Medicine and Immunology and Microbiology, Stanford University School of Medicine, Stanford, CA, 94305, USA.
O ThaunatCIRI, Centre International de Recherche en Infectiologie, Univ Lyon, Inserm, U1111, Université Claude Bernard Lyon 1, CNRS, UMR5308, ENS de Lyon, F-69007, Lyon, France.
T DefranceCIRI, Centre International de Recherche en Infectiologie, Univ Lyon, Inserm, U1111, Université Claude Bernard Lyon 1, CNRS, UMR5308, ENS de Lyon, F-69007, Lyon, France.
H PaidassiCIRI, Centre International de Recherche en Infectiologie, Univ Lyon, Inserm, U1111, Université Claude Bernard Lyon 1, CNRS, UMR5308, ENS de Lyon, F-69007, Lyon, France. helena.paidassi@inserm.fr.ORCID http://orcid.org/0000-0001-9915-4365
K LahlImmunology Section, Lund University, 221 48, Lund, Sweden. Katharina.lahl@med.lu.se.ORCID http://orcid.org/0000-0003-4919-331X
Université Claude Bernard Lyon 1 · FRLund University · SETechnical University of Denmark · DKBerlin Institute of Health at Charité - Universitätsmedizin Berlin · DECentre National de la Recherche Scientifique · FRUniversité Paris-Sud · FRVA Palo Alto Health Care System · US

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Secretory intestinal IgA can protect from re-infection with rotavirus (RV), but very little is known about the mechanisms that induce IgA production during intestinal virus infections. Classical dendritic cells (cDCs) in the intestine can facilitate both T cell-dependent and -independent secretory IgA. Here, we show that BATF3-dependent cDC1, but not cDC2, are critical for the optimal induction of RV-specific IgA responses in the mesenteric lymph nodes. This depends on the selective expression of the TGFβ-activating integrin αvβ8 by cDC1. In contrast, αvβ8 on cDC1 is dispensible for steady state immune homeostasis. Given that cDC2 are crucial in driving IgA during steady state but are dispensable for RV-specific IgA responses, we propose that the capacity of DC subsets to induce intestinal IgA responses reflects the context, as opposed to an intrinsic property of individual DC subsets.

Indexed as

Antibodies, ViralAntibody SpecificityBasic-Leucine Zipper Transcription FactorsCytokinesDendritic CellsHost-Pathogen InteractionsImmunoglobulin AImmunoglobulin A, SecretoryIntegrinsRotavirusRotavirus InfectionsAntibodies, ViralBasic-Leucine Zipper Transcription FactorsCytokinesImmunoglobulin AImmunoglobulin A, Secretoryintegrin alphavbeta8Integrins

Identifiers

PMID32161355
OpenAlexW3011050535

What OpenQuestion holds

Textmetadata
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.