Evidence map›Paper›PMID 26795247›Full record

ArticleImmunity2016

A Temporal Switch in the Germinal Center Determines Differential Output of Memory B and Plasma Cells.

Florian J Weisel, Griselda V Zuccarino-Catania, Maria Chikina, Mark J Shlomchik

Open access · bronzeAbstract read
In one paragraph

Article in Immunity, 2016. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 347 papers.

0numbers the graph read from it
0cells of the map it votes in
347citing papers in PubMed
24.9field-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

347 citing papers in PubMed, 521 citations in OpenAlex.

  1. Adaptive Immunity in Marsupials.Journal of experimental zoology. Part A, Ecological and integrative physiology · 2026
    Review
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  16. Extrafollicular and other non-germinal center B cell responses.Journal of immunology (Baltimore, Md. : 1950) · 2026
    Review
  17. The multilayered identity of B cell memory.Cellular & molecular immunology · 2026
    Review
  18. Review
  19. Memory B cell development in response to mRNA SARS-CoV-2 and nanoparticle immunization in mice.Proceedings of the National Academy of Sciences of the United States of America · 2026
    Article
  20. HemaSphere · 2026
    Article

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

4 · The record

Corrections and comments

5 · Who and what money

Authors and funding

4 authors at 2 institutions in 1 country.

Florian J WeiselDepartment of Laboratory Medicine, Yale University School of Medicine, New Haven, CT 06520, USA; Department of Immunology, University of Pittsburgh School of Medicine, Pittsburgh, PA 15261, USA.
Griselda V Zuccarino-CataniaDepartment of Laboratory Medicine, Yale University School of Medicine, New Haven, CT 06520, USA.
Maria ChikinaDepartment of Computational and Systems Biology, University of Pittsburgh School of Medicine, Pittsburgh, PA 15260, USA.
Mark J ShlomchikDepartment of Laboratory Medicine, Yale University School of Medicine, New Haven, CT 06520, USA; Department of Immunology, University of Pittsburgh School of Medicine, Pittsburgh, PA 15261, USA; Department of Immunobiology, Yale University School of Medicine, New Haven, CT 06520, USA. Electronic address: mshlomch@pitt.edu.
University of Pittsburgh · USYale University · US

Funding

Yale Pathology Tissue Services Shared ResourceP30CA016359 · NCI · YALE UNIVERSITY · PI DAVID L RIMM · 1985 to 2026
$85.0M
Murine Memory B Cell Development and FunctionR01AI043603 · NIAID · YALE UNIVERSITY · PI MARK J SHLOMCHIK · 1998 to 2026
$9.7M
Signaling and Selection in Germinal Center B CellsR01AI105018 · NIAID · UNIVERSITY OF PITTSBURGH AT PITTSBURGH · PI MARK J SHLOMCHIK · 2014 to 2026
$4.8M
LSRII Flow Cytometric AnalyzerS10RR023431 · NCRR · YALE UNIVERSITY · PI SHLOMCHIK, MARK J · 2007 to 2007
$339k
NCI NIH HHS P30 CA016359NCRR NIH HHS S10 RR023431NIAID NIH HHS R01 AI043603NIAID NIH HHS R01 AI105018PHS HHS R01-AL46303
6 · The paper itself

Abstract

There is little insight into or agreement about the signals that control differentiation of memory B cells (MBCs) and long-lived plasma cells (LLPCs). By performing BrdU pulse-labeling studies, we found that MBC formation preceded the formation of LLPCs in an adoptive transfer immunization system, which allowed for a synchronized Ag-specific response with homogeneous Ag-receptor, yet at natural precursor frequencies. We confirmed these observations in wild-type (WT) mice and extended them with germinal center (GC) disruption experiments and variable region gene sequencing. We thus show that the GC response undergoes a temporal switch in its output as it matures, revealing that the reaction engenders both MBC subsets with different immune effector function and, ultimately, LLPCs at largely separate points in time. These data demonstrate the kinetics of the formation of the cells that provide stable humoral immunity and therefore have implications for autoimmunity, for vaccine development, and for understanding long-term pathogen resistance.

Indexed as

Adoptive TransferAnimalsB-LymphocytesB-Lymphocyte SubsetsCell DifferentiationCell SeparationEnzyme-Linked Immunospot AssayFlow CytometryGerminal CenterImmunity, HumoralImmunohistochemistryImmunologic MemoryMiceMice, Inbred BALB CMice, TransgenicPlasma Cells

Identifiers

PMID26795247
PMCPMC4724390
OpenAlexW2239291357

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.