Evidence map›Paper›PMID 20505142›Full record

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

Constitutive CD40L expression on B cells prematurely terminates germinal center response and leads to augmented plasma cell production in T cell areas.

Anna Bolduc, Eugene Long, Dale Stapler, Marilia Cascalho, Takeshi Tsubata, Pandelakis A Koni, Michiko Shimoda

Erratum issuedOpen access · bronzeAbstract readComparative Study
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. An erratum has been issued. Cited by 28 papers.

0numbers the graph read from it
0cells of the map it votes in
28citing papers in PubMed
1.4field-weighted citation impact, top 20% 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

28 citing papers in PubMed, 41 citations in OpenAlex.

  1. Review
  2. Article
  3. Review
  4. Review
  5. Article
  6. Article
  7. Article
  8. Review
  9. Germinal Centre Shutdown.Frontiers in immunology · 2021
    Review
  10. Review
  11. Review
  12. Article
  13. Article
  14. Article
  15. Article
  16. Article
  17. Review
  18. The Role of TLR4 on B Cell Activation and Anti-Journal of immunology research · 2016
    Review
  19. Innovative agents in multiple myeloma.Journal of the advanced practitioner in oncology · 2014
    Review
  20. Review
4 · The record

Corrections and comments

  • Erratum issued
5 · Who and what money

Authors and funding

7 authors at 3 institutions in 2 countries.

Anna BolducImmunotherapy Center, Medical College of Georgia, Augusta, GA 30912, USA.
Eugene Long
Dale Stapler
Marilia Cascalho
Takeshi Tsubata
Pandelakis A Koni
Michiko Shimoda
Augusta University · USMichigan Medicine · USTokyo Medical and Dental University · JP

Funding

T cell responses and cardiac transplantation in infancyP01HL079067 · NHLBI · UNIVERSITY OF MICHIGAN AT ANN ARBOR · PI PLATT, JEFFREY L · 2005 to 2009
$6.3M
Long-lived plasma cell differentiationR21AI064752 · NIAID · AUGUSTA UNIVERSITY · PI SHIMODA, MICHIKO · 2007 to 2008
$401k
Beta cell antigen presentation in models of Beta cell a*R03AR052470 · NIAMS · AUGUSTA UNIVERSITY · PI SHIMODA, MICHIKO · 2006 to 2008
$214k
NHLBI NIH HHS HL079067NIAID NIH HHS AI064752NIAID NIH HHS R21 AI064752NIAMS NIH HHS AR052470NIAMS NIH HHS R03 AR052470
6 · The paper itself

Abstract

CD40/CD40L engagement is essential to T cell-dependent B cell proliferation and differentiation. However, the precise role of CD40 signaling through cognate T-B interaction in the generation of germinal center and memory B cells is still incompletely understood. To address this issue, a B cell-specific CD40L transgene (CD40LBTg) was introduced into mice with B cell-restricted MHC class II deficiency. Using this mouse model, we show that constitutive CD40L expression on B cells alone could not induce germinal center differentiation of MHC class II-deficient B cells after immunization with T cell-dependent Ag. Thus, some other MHC class II-dependent T cell-derived signals are essential for the generation of germinal center B cells in response to T cell-dependent Ag. In fact, CD40LBTg mice generated a complex Ag-specific IgG1 response, which was greatly enhanced in early, but reduced in late, primary response compared with control mice. We also found that the frequency of Ag-specific germinal center B cells in CD40LBTg mice was abruptly reduced 1 wk after immunization. As a result, the numbers of Ag-specific IgG1 long-lived plasma cells and memory B cells were reduced. By histology, large numbers of Ag-specific plasma cells were found in T cell areas adjacent to Ag-specific germinal centers of CD40LBTg mice, temporarily during the second week of primary response. These results indicate that CD40L expression on B cells prematurely terminated their ongoing germinal center response and produced plasma cells. Our results support the notion that CD40 signaling is an active termination signal for germinal center reaction.

Indexed as

Adjuvants, ImmunologicAnimalsB-Lymphocyte SubsetsCD40 AntigensCD40 LigandCells, CulturedDisease Models, AnimalDown-RegulationEpitopes, B-LymphocyteGerminal CenterHistocompatibility Antigens Class IIHumansImmunoglobulin GMiceMice, Inbred C57BLMice, TransgenicAdjuvants, ImmunologicCD40 AntigensCD40 LigandEpitopes, B-LymphocyteHistocompatibility Antigens Class IIImmunoglobulin G

Identifiers

PMID20505142
PMCPMC3708602
OpenAlexW1877571168

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.