Evidence map›Paper›PMID 37133336›Full record

ArticleJournal of immunology (Baltimore, Md. : 1950)2023

Cutting Edge: IL-21 and Tissue-Specific Signals Instruct Tbet+CD11c+ B Cell Development following Viral Infection.

Wenzhi Song, Gina M Sanchez, Daniel P Mayer, Holly N Blackburn, Irene Chernova, Richard A Flavell, Jason S Weinstein, Joe Craft

Open access · greenAbstract read
In one paragraph

Article in Journal of immunology (Baltimore, Md. : 1950), 2023. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 9 papers.

0numbers the graph read from it
0cells of the map it votes in
9citing papers in PubMed
2.5field-weighted citation impact, top 11% 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

9 citing papers in PubMed, 15 citations in OpenAlex.

  1. Review
  2. Review
  3. Review
  4. Extrafollicular and other non-germinal center B cell responses.Journal of immunology (Baltimore, Md. : 1950) · 2026
    Review
  5. Article
  6. Article
  7. Review
  8. Review
  9. Polarization of the memory B-cell response.Journal of leukocyte biology · 2025
    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

8 authors at 3 institutions in 1 country.

Wenzhi SongDepartment of Immunobiology, Yale University School of Medicine, New Haven, CT.ORCID 0000-0001-6969-7019
Gina M SanchezCenter for Immunity and Inflammation, Rutgers New Jersey Medical School, Newark, NJ.ORCID 0000-0001-7807-1069
Daniel P MayerCenter for Immunity and Inflammation, Rutgers New Jersey Medical School, Newark, NJ.
Holly N BlackburnDepartment of Immunobiology, Yale University School of Medicine, New Haven, CT.ORCID 0000-0003-2759-3216
Irene ChernovaDepartment of Internal Medicine, Yale University School of Medicine; New Haven, CT.ORCID 0000-0003-3346-0559
Richard A FlavellDepartment of Immunobiology, Yale University School of Medicine, New Haven, CT.ORCID 0000-0003-4461-0778
Jason S WeinsteinCenter for Immunity and Inflammation, Rutgers New Jersey Medical School, Newark, NJ.
Joe CraftDepartment of Immunobiology, Yale University School of Medicine, New Haven, CT.ORCID 0000-0002-1368-6756
Yale University · USRutgers, The State University of New Jersey · USHoward Hughes Medical Institute · US

Funding

Yale Clinical and Translational Science Award (U Component)UL1TR001863 · NCATS · YALE UNIVERSITY · PI John H. Krystal, LUCILA OHNO-MACHADO · 2016 to 2026
$102.9M
IMMUNE RESPONSES IN LUPUSR37AR040072 · NIAMS · YALE UNIVERSITY · PI CRAFT, JOSEPH EDGAR · 2000 to 2025
$7.4M
T cell regulation of pathogenic B cells in systemic autoimmunityR01AR073912 · NIAMS · RUTGERS BIOMEDICAL AND HEALTH SCIENCES · PI Jason Weinstein · 2018 to 2026
$3.2M
Follicular Helper T Cell Function in AutoimmunityR01AR074545 · NIAMS · YALE UNIVERSITY · PI CRAFT, JOSEPH EDGAR · 2019 to 2022
$1.3M
Transcriptional Regulation of T Follicular Helper Cells in LupusK01AR067892 · NIAMS · YALE UNIVERSITY · PI WEINSTEIN, JASON · 2015 to 2019
$614k
NCATS NIH HHS UL1 TR001863NIAMS NIH HHS K01 AR067892NIAMS NIH HHS R01 AR073912NIAMS NIH HHS R01 AR074545NIAMS NIH HHS R37 AR040072
6 · The paper itself

Abstract

Tbet+CD11c+ B cells, also known as age-associated B cells (ABCs), are pivotal contributors to humoral immunity following infection and in autoimmunity, yet their in vivo generation is incompletely understood. We used a mouse model of systemic acute lymphocytic choriomeningitis virus infection to examine the developmental requirements of ABCs that emerged in the spleen and liver. IL-21 signaling through STAT3 was indispensable for ABC development. In contrast, IFN-γ signaling through STAT1 was required for B cell activation and proliferation. Mice that underwent splenectomy or were deficient in lymphotoxin α generated hepatic ABCs despite the lack of secondary lymphoid organ contributions, suggesting that the liver supported de novo generation of these cells separately from their development in lymphoid organs. Thus, IFN-γ and IL-21 signaling have distinct, stage-specific roles in ABC differentiation, while the tissue microenvironment provides additional cues necessary for their development.

Indexed as

InterleukinsLymphocytic ChoriomeningitisAnimalsCell DifferentiationInterleukin-21MiceMice, Inbred C57BLMice, KnockoutInterleukin-21Interleukins

Identifiers

PMID37133336
PMCPMC10247523
OpenAlexW4367834265

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.