Evidence map›Paper›PMID 25957170›Full record

ArticleJournal of immunology (Baltimore, Md. : 1950)2015

Cutting edge: T follicular helper cell differentiation is defective in the absence of Bcl6 BTB repressor domain function.

J Philip Nance, Simon Bélanger, Robert J Johnston, Toshitada Takemori, Shane Crotty

Open access · bronzeAbstract read
In one paragraph

Article in Journal of immunology (Baltimore, Md. : 1950), 2015. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 25 papers.

0numbers the graph read from it
0cells of the map it votes in
25citing papers in PubMed
2.1field-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

25 citing papers in PubMed, 33 citations in OpenAlex.

  1. Article
  2. Article
  3. B Cell Lymphoma 6 (BCL6): A Conserved Regulator of Immunity and Beyond.International journal of molecular sciences · 2024
    Review
  4. Transcriptional programming of CD4Science immunology · 2023
    Article
  5. Article
  6. Article
  7. Review
  8. Review
  9. Review
  10. Review
  11. Review
  12. Article
  13. Highly Efficient and Versatile Plasmid-Based Gene Editing in Primary T Cells.Journal of immunology (Baltimore, Md. : 1950) · 2018
    Article
  14. Article
  15. Repression of miR-31 by BCL6 stabilizes the helper function of human follicular helper T cells.Proceedings of the National Academy of Sciences of the United States of America · 2017
    Article
  16. Article
  17. Article
  18. Review
  19. Article
  20. CXCL13 is a plasma biomarker of germinal center activity.Proceedings of the National Academy of Sciences of the United States of America · 2016
    Article
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

5 authors at 2 institutions in 2 countries.

J Philip NanceDivision of Vaccine Discovery, La Jolla Institute of Allergy and Immunology, La Jolla, CA 92037;
Simon BélangerDivision of Vaccine Discovery, La Jolla Institute of Allergy and Immunology, La Jolla, CA 92037;
Robert J JohnstonGenentech, South San Francisco, CA 94080; and.
Toshitada TakemoriRIKEN Research Center for Allergy and Immunology, Yokohama City, Kanagawa 230-0045, Japan.
Shane CrottyDivision of Vaccine Discovery, La Jolla Institute of Allergy and Immunology, La Jolla, CA 92037; shane@lji.org.
La Jolla Institute for Immunology · USRIKEN Center for Integrative Medical Sciences · JP

Funding

TF regulation of CD8 and CD4 T cell memory in both systemic and dermal infectionU19AI109976 · NIAID · LA JOLLA INSTITUTE FOR IMMUNOLOGY · PI CROTTY, SHANE P · 2014 to 2018
$10.5M
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 AI072543NIAID NIH HHS U19 AI109976
6 · The paper itself

Abstract

T follicular helper (Tfh) cells are essential for germinal centers (GCs) and most long-term humoral immunity. Differentiation of Tfh cells depends on the transcriptional repressor B cell CLL/lymphoma 6 (Bcl6). Bcl6 mediates gene repression via the recruitment of corepressors. Currently, it is unknown how Bcl6 recruits corepressors to regulate gene expression of Tfh cells. In this article, we demonstrate, using a mutant form of Bcl6 with two BTB (bric-a-brac, tramtrack, broad-complex) mutations that abrogate corepressor binding, that the Bcl6 BTB domain is required for proper differentiation of Tfh and GC-Tfh cells in vivo. Importantly, we also observe a significant defect in GC B cell development. These results are consistent in multiple contexts, including a novel lymphocytic choriomeningitis virus nucleoprotein-specific TCR-transgenic mouse model. Taken together, these data suggest that the Bcl6 BTB domain is a key mediator of the differentiation of Tfh cells.

Indexed as

Cell DifferentiationProtein Interaction Domains and MotifsAnimalsB-LymphocytesGerminal CenterLymphocyte ActivationMiceMice, TransgenicProtein BindingProto-Oncogene Proteins c-bcl-6T-Lymphocytes, Helper-InducerT-Lymphocyte SubsetsProto-Oncogene Proteins c-bcl-6

Identifiers

PMID25957170
PMCPMC4456636
OpenAlexW1669328016

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.