Evidence map›Paper›PMID 28768709›Full record

ArticleThe Journal of experimental medicine2017

Co-stimulatory function in primary germinal center responses: CD40 and B7 are required on distinct antigen-presenting cells.

Masashi Watanabe, Chiharu Fujihara, Andrea J Radtke, Y Jeffrey Chiang, Sumeena Bhatia, Ronald N Germain, Richard J Hodes

Abstract read
In one paragraph

Article in The Journal of experimental medicine, 2017. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 37 papers.

0numbers the graph read from it
0cells of the map it votes in
37citing papers in PubMed
3.1field-weighted citation impact, top 8% 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

37 citing papers in PubMed, 57 citations in OpenAlex.

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  8. Unraveling the enigma: housekeeping geneFrontiers in psychiatry · 2024
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  13. Contribution of Dendritic Cell Subsets to T Cell-Dependent Responses in Mice.Journal of immunology (Baltimore, Md. : 1950) · 2022
    Article
  14. Review
  15. B Cell-Intrinsic IRF4 Haploinsufficiency Impairs Affinity Maturation.Journal of immunology (Baltimore, Md. : 1950) · 2021
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  18. Superior inhibition of alloantibody responses with selective CD28 blockade is CTLA-4 dependent and T follicular helper cell specific.American journal of transplantation : official journal of the American Society of Transplantation and the American Society of Transplant Surgeons · 2021
    Article
  19. Article
  20. 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 1 institution in 1 country.

Masashi WatanabeExperimental Immunology Branch, National Cancer Institute, National Institutes of Health, Bethesda, MD.
Chiharu FujiharaExperimental Immunology Branch, National Cancer Institute, National Institutes of Health, Bethesda, MD.ORCID http://orcid.org/0000-0003-0556-9530
Andrea J RadtkeLaboratory of Systems Biology, National Institute of Allergy and Infectious Diseases, National Institutes of Health, Bethesda, MD.
Y Jeffrey ChiangExperimental Immunology Branch, National Cancer Institute, National Institutes of Health, Bethesda, MD.
Sumeena BhatiaExperimental Immunology Branch, National Cancer Institute, National Institutes of Health, Bethesda, MD.
Ronald N GermainLaboratory of Systems Biology, National Institute of Allergy and Infectious Diseases, National Institutes of Health, Bethesda, MD.
Richard J HodesExperimental Immunology Branch, National Cancer Institute, National Institutes of Health, Bethesda, MD hodesr@31.nia.nih.gov.ORCID http://orcid.org/0000-0002-8142-5742
National Institutes of Health · US

Funding

Functional Biology Of T CellsZIAAI000758 · NIAID · NATIONAL INSTITUTE OF ALLERGY AND INFECTIOUS DISEASES · PI GERMAIN, RONALD N · 2009 to 2025
$15.4M
Receptor Mediated T and B Cell ActivationZIABC009281 · NCI · DIVISION OF BASIC SCIENCES - NCI · PI HODES, RICHARD J. · 2009 to 2023
$8.0M
6 · The paper itself

Abstract

T cell-dependent germinal center (GC) responses require coordinated interactions of T cells with two antigen-presenting cell (APC) populations, B cells and dendritic cells (DCs), in the presence of B7- and CD40-dependent co-stimulatory pathways. Contrary to the prevailing paradigm, we found unique cellular requirements for B7 and CD40 expression in primary GC responses to vaccine immunization with protein antigen and adjuvant: B7 was required on DCs but was not required on B cells, whereas CD40 was required on B cells but not on DCs in the generation of antigen-specific follicular helper T cells, antigen-specific GC B cells, and high-affinity class-switched antibody production. There was, in fact, no requirement for coexpression of B7 and CD40 on the same cell in these responses. Our findings support a substantially revised model for co-stimulatory function in the primary GC response, with crucial and distinct contributions of B7- and CD40-dependent pathways expressed by different APC populations and with important implications for understanding how to optimize vaccine responses or limit autoimmunity.

Indexed as

AnimalsAntibody FormationAntigen-Presenting CellsB7 AntigensB-LymphocytesCD40 AntigensDendritic CellsGerminal CenterImmunoglobulin GMiceMice, Inbred C57BLMice, KnockoutT-Cell Antigen Receptor SpecificityT-LymphocytesB7 AntigensCD40 AntigensImmunoglobulin G

Identifiers

PMID28768709
PMCPMC5584122
OpenAlexW2744015319

What OpenQuestion holds

Textmetadata
LicenceCC BY-NC-SA
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.