Evidence map›Paper›PMID 32610078›Full record

ArticleImmunity2020

Neonatal Exposure to Commensal-Bacteria-Derived Antigens Directs Polysaccharide-Specific B-1 B Cell Repertoire Development.

J Stewart New, Brian L P Dizon, Christopher F Fucile, Alexander F Rosenberg, John F Kearney, R Glenn King

Open access · bronzeAbstract read
In one paragraph

Article in Immunity, 2020. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 41 papers.

0numbers the graph read from it
0cells of the map it votes in
41citing papers in PubMed
4.2field-weighted citation impact, top 5% 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

41 citing papers in PubMed, 84 citations in OpenAlex.

  1. Review
  2. Article
  3. Review
  4. Article
  5. Review
  6. Posttranscriptional control of the B cell receptor by HuR is essential for innate B cell maintenance and function.Proceedings of the National Academy of Sciences of the United States of America · 2025
    Article
  7. Article
  8. Review
  9. Article
  10. Neonatal SARS-CoV-2 mRNA Vaccination Efficacy Is Influenced by Maternal Antibodies.American journal of reproductive immunology (New York, N.Y. : 1989) · 2024
    Article
  11. Review
  12. Review
  13. Glycan-Reactive Innate-like B Cells and Developmental Checkpoints.Journal of immunology (Baltimore, Md. : 1950) · 2024
    Article
  14. Article
  15. Article
  16. Review
  17. Noncanonical B Cells: Characteristics of Uncharacteristic B Cells.Journal of immunology (Baltimore, Md. : 1950) · 2023
    Review
  18. Article
  19. Article
  20. Article
4 · The record

Corrections and comments

5 · Who and what money

Authors and funding

6 authors at 2 institutions in 1 country.

J Stewart NewDepartment of Microbiology, University of Alabama at Birmingham, Birmingham, AL 35294, USA.
Brian L P DizonDepartment of Microbiology, University of Alabama at Birmingham, Birmingham, AL 35294, USA; National Institutes of Arthritis and Musculoskeletal and Skin Diseases, National Institutes of Health, Bethesda, MD 20892, USA.
Christopher F FucileInformatics Institute, University of Alabama at Birmingham, Birmingham, AL 35294, USA.
Alexander F RosenbergDepartment of Microbiology, University of Alabama at Birmingham, Birmingham, AL 35294, USA; Informatics Institute, University of Alabama at Birmingham, Birmingham, AL 35294, USA.
John F KearneyDepartment of Microbiology, University of Alabama at Birmingham, Birmingham, AL 35294, USA. Electronic address: jfk@uab.edu.
R Glenn KingDepartment of Microbiology, University of Alabama at Birmingham, Birmingham, AL 35294, USA. Electronic address: rgking@uab.edu.
University of Alabama at Birmingham · USNational Institutes of Health · US

Funding

XRAY CRYSTALLOGRAPHYP30CA013148 · NCI · UNIVERSITY OF ALABAMA AT BIRMINGHAM · PI Robert S Welner · 1985 to 2026
$165.9M
Virology CoreP30AI027767 · NIAID · UNIVERSITY OF ALABAMA AT BIRMINGHAM · PI Latesha Ellen Elopre · 1988 to 2026
$84.1M
UAB Center for Clinical and Translational Science (CCTS)UL1TR001417 · NCATS · UNIVERSITY OF ALABAMA AT BIRMINGHAM · PI KIMBERLY, ROBERT P. · 2015 to 2018
$31.4M
CELLULAR &MOLECULAR BASIS OF DISEASE TRAINING PROGRAMT32GM008061 · NIGMS · NORTHWESTERN UNIVERSITY · PI CARTHEW, RICHARD W. · 1985 to 2022
$17.1M
IMMUNOLOGIC DISEASES AND BASIC IMMUNOLOGYT32AI007051 · NIAID · UNIVERSITY OF ALABAMA AT BIRMINGHAM · PI Laurie Ellen Harrington · 1985 to 2026
$13.1M
ROS Modulation of Innate and Adaptive Immunity in RAP30AR048311 · NIAMS · UNIVERSITY OF ALABAMA AT BIRMINGHAM · PI MOUNTZ, JOHN D · 2001 to 2017
$9.5M
Regulation of B cell Clonal Diversity and Its Role in DiseaseR01AI014782 · NIAID · UNIVERSITY OF ALABAMA AT BIRMINGHAM · PI KEARNEY, JOHN FRANKLIN · 1985 to 2020
$7.1M
Effects of neonatal microbial exposure on anti-polysaccharide B cell developmentU01AI100005 · NIAID · UNIVERSITY OF ALABAMA AT BIRMINGHAM · PI KEARNEY, JOHN FRANKLIN · 2017 to 2021
$1.9M
Developing and Improving the UAB Gnotobiotic Facility.G20OD016623 · OD · UNIVERSITY OF ALABAMA AT BIRMINGHAM · PI CARTNER, SAMUEL CORBIN · 2013 to 2013
$496k
Modulation of Autoimmune Diabetes by N-acetyl-D-glucosamine Specific B cellsF30DK082277 · NIDDK · UNIVERSITY OF ALABAMA AT BIRMINGHAM · PI DIZON, BRIAN LEONARD · 2008 to 2010
$99k
Commensal-dependent maturation of the natural IgM repertoireF31AI120500 · NIAID · UNIVERSITY OF ALABAMA AT BIRMINGHAM · PI NEW, JAMES STEWART · 2015 to 2017
$80k
NCATS NIH HHS UL1 TR001417NCI NIH HHS P30 CA013148NIAID NIH HHS F31 AI120500NIAID NIH HHS P30 AI027767NIAID NIH HHS R01 AI014782NIAID NIH HHS T32 AI007051NIAID NIH HHS U01 AI100005NIAMS NIH HHS P30 AR048311NIDDK NIH HHS F30 DK082277NIGMS NIH HHS T32 GM008061NIH HHS G20 OD016623
6 · The paper itself

Abstract

B-1 B cells derive from a developmental program distinct from that of conventional B cells, through B cell receptor (BCR)-dependent positive selection of fetally derived precursors. Here, we used direct labeling of B cells reactive with the N-acetyl-D-glucosamine (GlcNAc)-containing Lancefield group A carbohydrate of Streptococcus pyogenes to study the effects of bacterial antigens on the emergent B-1 B cell clonal repertoire. The number, phenotype, and BCR clonotypes of GlcNAc-reactive B-1 B cells were modulated by neonatal exposure to heat-killed S. pyogenes bacteria. GlcNAc-reactive B-1 clonotypes and serum antibodies were reduced in germ-free mice compared with conventionally raised mice. Colonization of germ-free mice with a conventional microbiota promoted GlcNAc-reactive B-1 B cell development and concomitantly elicited clonally related IgA

Indexed as

AcetylglucosamineAnimalsAnimals, NewbornAntibodies, BacterialAntigens, BacterialB-Lymphocyte SubsetsGerm-Free LifeMiceMice, Inbred C57BLMice, KnockoutMicrobiotaPolysaccharides, BacterialStreptococcus pyogenesAcetylglucosamineAntibodies, BacterialAntigens, BacterialPolysaccharides, BacterialB-1 B cellsB cell repertoireinnate-like B cellsLancefield group A carbohydratemicrobiotaN-acetyl-D-glucosaminenatural antibodiesneonatal immunityStreptococcus pyogenes

Identifiers

PMID32610078
PMCPMC7971260
OpenAlexW3040264116

What OpenQuestion holds

Textmetadata
LicenceTDM
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.