Evidence map›Paper›PMID 25958842›Full record

ArticleCellular & molecular immunology2015

Function and regulation of self-reactive marginal zone B cells in autoimmune arthritis.

Anna-Karin E Palm, Heike C Friedrich, Anja Mezger, Maya Salomonsson, Linda K Myers, Sandra Kleinau

Open access · bronzeAbstract read
In one paragraph

Article in Cellular & molecular immunology, 2015. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 18 papers.

0numbers the graph read from it
0cells of the map it votes in
18citing papers in PubMed
1.0field-weighted citation impact, top 26% 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

18 citing papers in PubMed, 30 citations in OpenAlex.

  1. Article
  2. Article
  3. Article
  4. Defining two subpopulations of marginal zone B cells.Cellular & molecular immunology · 2024
    Article
  5. Article
  6. Review
  7. A B cell-driven EAE mouse model reveals the impact of B cell-derived cytokines on CNS autoimmunity.Proceedings of the National Academy of Sciences of the United States of America · 2023
    Article
  8. Article
  9. Review
  10. Review
  11. Homeostasis and regulation of autoreactive B cells.Cellular & molecular immunology · 2020
    Review
  12. Innate Lymphocytes in Inflammatory Arthritis.Frontiers in immunology · 2020
    Review
  13. Article
  14. The Promise of Anti-idiotype Revisited.Frontiers in immunology · 2019
    Review
  15. Review
  16. Review
  17. Article
  18. Article
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

6 authors at 2 institutions in 2 countries.

Anna-Karin E PalmDepartment of Cell and Molecular Biology, Uppsala University, Uppsala, Sweden.
Heike C FriedrichDepartment of Cell and Molecular Biology, Uppsala University, Uppsala, Sweden.
Anja MezgerDepartment of Cell and Molecular Biology, Uppsala University, Uppsala, Sweden.
Maya SalomonssonDepartment of Cell and Molecular Biology, Uppsala University, Uppsala, Sweden.
Linda K MyersDepartment of Pediatrics, University of Tennessee Health Science Center, Memphis, TN, USA.
Sandra KleinauDepartment of Cell and Molecular Biology, Uppsala University, Uppsala, Sweden.
Uppsala University · SEUniversity of Tennessee Health Science Center · US

Funding

20(OH) Vit D3, T Cells, and ArthritisR01AR064825 · NIAMS · UNIVERSITY OF TENNESSEE HEALTH SCI CTR · PI KANG, ANDREW H · 2014 to 2018
$1.6M
NIAMS NIH HHS R01 AR064825
6 · The paper itself

Abstract

Polyreactive innate-type B cells account for many B cells expressing self-reactivity in the periphery. Improper regulation of these B cells may be an important factor that underlies autoimmune disease. Here we have explored the influence of self-reactive innate B cells in the development of collagen-induced arthritis (CIA), a mouse model of rheumatoid arthritis. We show that splenic marginal zone (MZ), but not B-1 B cells exhibit spontaneous IgM reactivity to autologous collagen II in naı¨ve mice. Upon immunization with heterologous collagen II in complete Freund's adjuvant the collagen-reactive MZ B cells expanded rapidly, while the B-1 B cells showed a modest anti-collagen response. The MZ B cells were easily activated by toll-like receptor (TLR) 4 and 9-ligands in vitro, inducing proliferation and cytokine secretion, implying that dual engagement of the B-cell receptor and TLRs may promote the immune response to self-antigen. Furthermore, collagen-primed MZ B cells showed significant antigen-presenting capacity as reflected by cognate T-cell proliferation in vitro and induction of IgG anti-collagen antibodies in vivo. MZ B cells that were deficient in complement receptors 1 and 2 demonstrated increased proliferation and cytokine production, while Fcγ receptor IIb deficiency of the cells lead to increased cytokine production and antigen presentation. In conclusion, our data highlight self-reactive MZ B cells as initiators of the autoimmune response in CIA, where complement and Fc receptors are relevant in controlling the self-reactivity in the cells.

Indexed as

Cell ProliferationAnimalsArthritis, RheumatoidB-Lymphocyte SubsetsCollagenMiceMice, Mutant StrainsReceptors, IgGSpleenToll-Like Receptor 4Toll-Like Receptor 9CollagenFcgr2b protein, mouseReceptors, IgGTlr4 protein, mouseTlr9 protein, mouseToll-Like Receptor 4Toll-Like Receptor 9

Identifiers

PMID25958842
PMCPMC4496548
OpenAlexW1480811716

What OpenQuestion holds

Textmetadata
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.