Evidence map›Paper›PMID 18362174›Full record

ArticleThe Journal of experimental medicine2008

Distinct cell-specific control of autoimmunity and infection by FcgammaRIIb.

Rebecca J Brownlie, Kate E Lawlor, Heather A Niederer, Antony J Cutler, Zou Xiang, Menna R Clatworthy, R Andres Floto, David R Greaves, Paul A Lyons, Kenneth G C Smith

Open access · greenAbstract read
In one paragraph

Article in The Journal of experimental medicine, 2008. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 71 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
71citing papers in PubMed, 1 pooled it
11.1field-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

71 citing papers in PubMed, 1 synthesis or guideline pooled it, 164 citations in OpenAlex.

  1. Pooled it
  2. Review
  3. Review
  4. Article
  5. Article
  6. Article
  7. Frontiers in immunology · 2022
    Review
  8. Inhibition of B cell activation followingJournal of translational autoimmunity · 2021
    Article
  9. Review
  10. Article
  11. Macrophage metabolic reprogramming presents a therapeutic target in lupus nephritis.Proceedings of the National Academy of Sciences of the United States of America · 2020
    Article
  12. Article
  13. Article
  14. Article
  15. Article
  16. Article
  17. Article
  18. Review
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  20. Article

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

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

10 authors at 2 institutions in 1 country.

Rebecca J BrownlieCambridge Institute for Medical Research and the Department of Medicine, University of Cambridge School of Clinical Medicine, Addenbrooke's Hospital, Cambridge CB2 2OY, England, UK.
Kate E Lawlor
Heather A Niederer
Antony J Cutler
Zou Xiang
Menna R Clatworthy
R Andres Floto
David R Greaves
Paul A Lyons
Kenneth G C Smith
University of Cambridge · GBUniversity of Oxford · GB

Funding

Medical Research Council G108/485Wellcome Trust 06753AIAWellcome Trust 081020
6 · The paper itself

Abstract

FcgammaRIIb is an inhibitory Fc receptor expressed on B cells and myeloid cells. It is important in controlling responses to infection, and reduced expression or function predisposes to autoimmunity. To determine if increased expression of FcgammaRIIb can modulate these processes, we created transgenic mice overexpressing FcgammaRIIb on B cells or macrophages. Overexpression of FcgammaRIIb on B cells reduced the immunoglobulin G component of T-dependent immune responses, led to early resolution of collagen-induced arthritis (CIA), and reduced spontaneous systemic lupus erythematosus (SLE). In contrast, overexpression on macrophages had no effect on immune responses, CIA, or SLE but increased mortality after Streptococcus pneumoniae infection. These results help define the role of FcgammaRIIb in immune responses, demonstrate the contrasting roles played by FcgammaRIIb on B cells and macrophages in the control of infection and autoimmunity, and emphasize the therapeutic potential for modulation of FcgammaRIIb expression on B cells in inflammatory and autoimmune disease.

Indexed as

AnimalsAntigens, CDArthritis, ExperimentalAutoimmunityB7-2 AntigenBacterial InfectionsB-LymphocytesCell ProliferationExtracellular Signal-Regulated MAP KinasesHumansImmunoglobulin GInfectionsLupus Erythematosus, SystemicMacrophagesMiceMice, TransgenicAntigens, CDB7-2 AntigenExtracellular Signal-Regulated MAP KinasesFc gamma receptor IIBImmunoglobulin GReceptors, IgG

Identifiers

PMID18362174
PMCPMC2292226
OpenAlexW2108007494

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.