Evidence map›Paper›PMID 32751234›Full record

ArticleViruses2020

Regulatory B Lymphocytes Colonize the Respiratory Tract of Neonatal Mice and Modulate Immune Responses of Alveolar Macrophages to RSV Infection in IL-10-Dependant Manner.

Daphné Laubreton, Carole Drajac, Jean-François Eléouët, Marie-Anne Rameix-Welti, Richard Lo-Man, Sabine Riffault, Delphyne Descamps

Open access · goldAbstract read
In one paragraph

Article in Viruses, 2020. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 14 papers.

0numbers the graph read from it
0cells of the map it votes in
14citing papers in PubMed
1.9field-weighted citation impact, top 13% 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

14 citing papers in PubMed, 21 citations in OpenAlex.

  1. Review
  2. Review
  3. Review
  4. Review
  5. Review
  6. Review
  7. Review
  8. Review
  9. Review
  10. Review
  11. Review
  12. Article
  13. Review
  14. 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

7 authors at 3 institutions in 2 countries.

Daphné LaubretonUniversité Paris-Saclay, INRAE, UVSQ, VIM, 78350 Jouy-en-Josas, France.ORCID 0000-0001-9506-6755
Carole DrajacUniversité Paris-Saclay, INRAE, UVSQ, VIM, 78350 Jouy-en-Josas, France.ORCID 0000-0003-4728-9641
Jean-François EléouëtUniversité Paris-Saclay, INRAE, UVSQ, VIM, 78350 Jouy-en-Josas, France.
Marie-Anne Rameix-WeltiUniversité Paris-Saclay, UVSQ, Inserm, Infection et Inflammation, U1173, 78180 Montigny-Le-Bretonneux, France.ORCID 0000-0002-5901-3856
Richard Lo-ManThe Center for Microbes, Development and Health, Key Laboratory of Molecular Virology and Immunology, Unit Immunity and Pediatric Infectious Diseases, Institute Pasteur of Shanghai, Chinese Academy of Sciences, Shanghai 200031, China.
Sabine RiffaultUniversité Paris-Saclay, INRAE, UVSQ, VIM, 78350 Jouy-en-Josas, France.
Delphyne DescampsUniversité Paris-Saclay, INRAE, UVSQ, VIM, 78350 Jouy-en-Josas, France.ORCID 0000-0002-4883-6910
Université de Versailles Saint-Quentin-en-Yvelines · FRInserm · FRInstitut Pasteur of Shanghai · CN

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Respiratory syncytial virus (RSV) is the prevalent pathogen of lower respiratory tract infections in children. The presence of neonatal regulatory B lymphocytes (nBreg) has been associated with a poor control of RSV infection in human newborns and with bronchiolitis severity. So far, little is known about how nBreg may contribute to neonatal immunopathology to RSV. We tracked nBreg in neonatal BALB/c mice and we investigated their impact on lung innate immunity, especially their crosstalk with alveolar macrophages (AMs) upon RSV infection. We showed that the colonization by nBreg during the first week of life is a hallmark of neonatal lung whereas this population is almost absent in adult lung. This particular period of age when nBreg are abundant corresponds to the same period when RSV replication in lungs fails to generate a type-I interferons (IFN-I) response and is not contained. When neonatal AMs are exposed to RSV in vitro, they produce IFN-I that in turn enhances IL-10 production by nBreg. IL-10 reciprocally can decrease IFN-I secretion by AMs. Thus, our work identified nBreg as an important component of neonatal lungs and pointed out new immunoregulatory interactions with AMs in the context of RSV infection.

Indexed as

AnimalsAnimals, NewbornB-Lymphocytes, RegulatoryB-Lymphocyte SubsetsCells, CulturedImmunity, InnateInterferon Type IInterleukin-10LungMacrophages, AlveolarMiceMice, Inbred BALB CRespiratory Syncytial VirusesRespiratory Syncytial Virus InfectionsSpleenTurbinatesIL10 protein, mouseInterferon Type IInterleukin-10age-dependent replicationalveolar macrophageimmunoregulationinnate immunityinterferonsinterleukine-10lungsneonatesregulatory B-cellrespiratory syncytial virus

Identifiers

PMID32751234
PMCPMC7472339
OpenAlexW3045890190

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.