Evidence map›Paper›PMID 20525889›Full record

ArticleJournal of immunology (Baltimore, Md. : 1950)2010

Germinal center T follicular helper cell IL-4 production is dependent on signaling lymphocytic activation molecule receptor (CD150).

Isharat Yusuf, Robin Kageyama, Laurel Monticelli, Robert J Johnston, Daniel Ditoro, Kyle Hansen, Burton Barnett, Shane Crotty

Open access · bronzeAbstract read
In one paragraph

Article in Journal of immunology (Baltimore, Md. : 1950), 2010. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 258 papers.

0numbers the graph read from it
0cells of the map it votes in
258citing papers in PubMed
12.5field-weighted citation impact, top 1% 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

258 citing papers in PubMed, 405 citations in OpenAlex.

  1. Trial
  2. Incidence of B-cell Malignancies in Patients with Lung Cancer Receiving PD-1 Blockade Therapy.Clinical cancer research : an official journal of the American Association for Cancer Research · 2026
    Article
  3. Review
  4. Article
  5. Review
  6. Designing 5' UTR sequences improves the capacity of mRNA therapeutics in preclinical models of aging and obesity.Molecular therapy : the journal of the American Society of Gene Therapy · 2026
    Article
  7. Article
  8. Article
  9. Article
  10. Article
  11. Review
  12. Article
  13. Effect of Age on Xenobiotic-Induced Autoimmunity.bioRxiv : the preprint server for biology · 2025
    Article
  14. Review
  15. Review
  16. Article
  17. Article
  18. Article
  19. Lipid metabolism in B cell biology.Molecular oncology · 2024
    Review
  20. Article

198 more citing papers are in PubMed but not listed here.

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 2 institutions in 1 country.

Isharat YusufDivision of Vaccine Discovery, La Jolla Institute for Allergy and Immunology, School of Medicine, La Jolla, CA 92037, USA.
Robin Kageyama
Laurel Monticelli
Robert J Johnston
Daniel Ditoro
Kyle Hansen
Burton Barnett
Shane Crotty
La Jolla Institute for Immunology · USUniversity of California, San Diego · US

Funding

Tfh and SAP and T cell help to B cellsR01AI072543 · NIAID · LA JOLLA INSTITUTE FOR IMMUNOLOGY · PI CROTTY, SHANE P · 2008 to 2018
$4.6M
Mechanisms of humoral immunity development and function to the smallpox vaccineR01AI063107 · NIAID · LA JOLLA INSTITUTE FOR IMMUNOLOGY · PI CROTTY, SHANE P · 2005 to 2015
$4.4M
NIAID NIH HHS R01 AI063107NIAID NIH HHS R01 AI072543PHS HHS R01 063107PHS HHS R01 072543
6 · The paper itself

Abstract

CD4 T cell help is critical for the generation and maintenance of germinal centers (GCs), and T follicular helper (T(FH)) cells are the CD4 T cell subset required for this process. Signaling lymphocytic activation molecule (SLAM)-associated protein (SAP [SH2D1A]) expression in CD4 T cells is essential for GC development. However, SAP-deficient mice have only a moderate defect in T(FH) differentiation, as defined by common T(FH) surface markers. CXCR5(+) T(FH) cells are found within the GC, as well as along the boundary regions of T/B cell zones. In this study, we show that GC-associated T follicular helper (GC T(FH)) cells can be identified by their coexpression of CXCR5 and the GL7 epitope, allowing for phenotypic and functional analysis of T(FH) and GC T(FH) populations. GC T(FH) cells are a functionally discrete subset of further polarized T(FH) cells, with enhanced B cell help capacity and a specialized ability to produce IL-4 in a T(H)2-independent manner. Strikingly, SAP-deficient mice have an absence of the GC T(FH) cell subset and SAP(-) T(FH) cells are defective in IL-4 and IL-21 production. We further demonstrate that SLAM (Slamf1, CD150), a surface receptor that uses SAP signaling, is specifically required for IL-4 production by GC T(FH) cells. GC T(FH) cells require IL-4 and -21 production for optimal help to B cells. These data illustrate complexities of SAP-dependent SLAM family receptor signaling, revealing a prominent role for SLAM receptor ligation in IL-4 production by GC CD4 T cells but not in T(FH) cell and GC T(FH) cell differentiation.

Indexed as

AnimalsAntigens, CDB-Lymphocyte SubsetsCell DifferentiationCells, CulturedCoculture TechniquesGerminal CenterImmunophenotypingInterleukin-4Intracellular Signaling Peptides and ProteinsMiceMice, Inbred C57BLMice, KnockoutMice, TransgenicReceptors, Cell SurfaceSignaling Lymphocytic Activation Molecule Associated ProteinAntigens, CDInterleukin-4Intracellular Signaling Peptides and ProteinsReceptors, Cell SurfaceSh2d1a protein, mouseSignaling Lymphocytic Activation Molecule Associated ProteinSignaling Lymphocytic Activation Molecule Family Member 1Slamf1 protein, mouse

Identifiers

PMID20525889
PMCPMC2913439
OpenAlexW1853217298

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.