Evidence map›Paper›PMID 33119033›Full record

ArticleThe Journal of experimental medicine2021

BAFFR controls early memory B cell responses but is dispensable for germinal center function.

Angelica W Y Lau, Vivian M Turner, Katherine Bourne, Jana R Hermes, Tyani D Chan, Robert Brink

Open access · bronzeAbstract read
In one paragraph

Article in The Journal of experimental medicine, 2021. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 19 papers.

0numbers the graph read from it
0cells of the map it votes in
19citing papers in PubMed
1.8field-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

19 citing papers in PubMed, 33 citations in OpenAlex.

  1. Review
  2. Review
  3. The multilayered identity of B cell memory.Cellular & molecular immunology · 2026
    Review
  4. Article
  5. Article
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  7. Article
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  9. Article
  10. Review
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  12. NF-kB's contribution to B cell fate decisions.Frontiers in immunology · 2023
    Review
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  14. Review
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  16. Article
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4 · The record

Corrections and comments

5 · Who and what money

Authors and funding

6 authors at 1 institution in 1 country.

Angelica W Y LauImmunology Division, Garvan Institute of Medical Research, Darlinghurst, New South Wales, Australia.
Vivian M TurnerImmunology Division, Garvan Institute of Medical Research, Darlinghurst, New South Wales, Australia.
Katherine BourneImmunology Division, Garvan Institute of Medical Research, Darlinghurst, New South Wales, Australia.
Jana R HermesImmunology Division, Garvan Institute of Medical Research, Darlinghurst, New South Wales, Australia.
Tyani D ChanImmunology Division, Garvan Institute of Medical Research, Darlinghurst, New South Wales, Australia.
Robert BrinkImmunology Division, Garvan Institute of Medical Research, Darlinghurst, New South Wales, Australia.
Garvan Institute of Medical Research · AU

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

The TNF superfamily ligand BAFF maintains the survival of naive B cells by signaling through its surface receptor, BAFFR. Activated B cells maintain expression of BAFFR after they differentiate into germinal center (GC) or memory B cells (MBCs). However, the functions of BAFFR in these antigen-experienced B cell populations remain unclear. Here, we show that B cell-intrinsic BAFFR does not play a significant role in the survival or function of GC B cells or in the generation of the somatically mutated MBCs derived from them. Instead, BAFF/BAFFR signaling was required to generate the unmutated, GC-independent MBCs that differentiate directly from activated B cell blasts early in the response. Furthermore, amplification of BAFFR signaling in responding B cells did not affect GCs or the generation of GC-derived MBCs but greatly expanded the GC-independent MBC response. Although BAFF/BAFFR signaling specifically controlled the formation of the GC-independent MBC response, both types of MBCs required input from this pathway for optimal long-term survival.

Indexed as

AnimalsB-Cell Activating FactorB-Cell Activation Factor ReceptorB-LymphocytesGerminal CenterImmunologic MemoryMiceMice, Inbred C57BLSignal TransductionB-Cell Activating FactorB-Cell Activation Factor ReceptorTnfrsf13c protein, mouse

Identifiers

PMID33119033
PMCPMC7604765
OpenAlexW3095628511

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.