Evidence map›Paper›PMID 21665435›Full record

ReviewJournal of autoimmunity2011

To B or not to B: role of B cells in pathogenesis of arthritis in HLA transgenic mice.

Marshall Behrens, Michele Smart, David Luckey, Harvinder Luthra, Veena Taneja

Abstract readReview
In one paragraph

Review in Journal of autoimmunity, 2011. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 14 papers.

0numbers the graph read from it
0cells of the map it votes in
14citing papers in PubMed
2.1field-weighted citation impact, top 13% 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

14 citing papers in PubMed, 25 citations in OpenAlex.

  1. Article
  2. Article
  3. Article
  4. Review
  5. Article
  6. Article
  7. Article
  8. Gender-biased regulation of human IL-17-producing cellsJournal of immune based therapies, vaccines and antimicrobials · 2013
    Article
  9. The autoimmune side of heart and lung diseases.Clinical reviews in allergy & immunology · 2013
    Review
  10. Article
  11. To B or not to B the conductor of rheumatoid arthritis orchestra.Clinical reviews in allergy & immunology · 2012
    Review
  12. Mincle and human B cell function.Journal of autoimmunity · 2012
    Article
  13. Review
  14. Autoimmunity in 2011.Clinical reviews in allergy & immunology · 2012
    Review
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

5 authors at 1 institution in 1 country.

Marshall BehrensDepartment of Immunology, Mayo Clinic College of Medicine, Rochester, MN 55905, United States.
Michele Smart
David Luckey
Harvinder Luthra
Veena Taneja
Mayo Clinic · US

Funding

IMMUNOGENETICS OF COLLAGEN-INDUCED ARTHRITIS IN MICER01AR030752 · NIAMS · MAYO CLINIC ROCHESTER · PI DAVID, CHELLA S, TANEJA, VEENA · 1987 to 2014
$4.3M
Role of B cells in pathogenesis of Collagen-induced Arthritis in Humanized MiceR01AI075262 · NIAID · MAYO CLINIC ROCHESTER · PI TANEJA, VEENA · 2009 to 2012
$1.2M
Impact of smoking on immune response and arthritis in humanized miceR21AR060077 · NIAMS · MAYO CLINIC ROCHESTER · PI TANEJA, VEENA · 2010 to 2011
$379k
Immunogenetics of Collagen Induced Arthritis in MiceR56AR030752 · NIAMS · MAYO CLINIC ROCHESTER · PI DAVID, CHELLA S, TANEJA, VEENA · 2009 to 2009
$325k
NIAID NIH HHS AI 75262NIAID NIH HHS R01 AI075262NIAMS NIH HHS AR30752NIAMS NIH HHS AR60077NIAMS NIH HHS R01 AR030752NIAMS NIH HHS R21 AR060077NIAMS NIH HHS R56 AR030752
6 · The paper itself

Abstract

Population studies have shown that amongst all the genetic factors linked with autoimmune disease development, MHC class II genes are the most significant. Experimental autoimmune arthritis resembling human rheumatoid arthritis (RA) can be induced in susceptible strains of mice following immunization with type II collagen (CIA). We generated transgenic mice lacking endogenous class II molecules and expressing various HLA genes including RA-associated, HLA-DRB1*0401 and HLA-DQ8, and RA-resistant, DRB1*0402, genes. The HLA molecules in these mice are expressed on the cell surface and can positively select CD4+ T cells expressing various Vβ T cell receptors. Endogenous class II invariant chain is required for proper functioning of the class II transgene. Arthritis development in transgenic mice is CD4+ and B cells dependent. Studies in humanized mice showed that B cells are required as antigen presenting cells in addition to antibody producing cells for the development of CIA. The transgenic mice expressing *0401 and *0401/DQ8 genes developed sex-biased arthritis with predominantly females being affected, similar to that of human RA. Further, the transgenic mice produced autoantibodies like rheumatoid factor and anti-cyclic antibodies. Antigen presentation by B cells leads to a sex-specific immune response in DRB1*0401 mice suggesting a role of B cells and HLA-DR in rendering susceptibility to develop arthritis in females.

Indexed as

AnimalsAntigen PresentationArthritisAutoantibodiesB-LymphocytesCD4-Positive T-LymphocytesCollagen Type IIDisease Models, AnimalFemaleGenetic Predisposition to DiseaseHLA AntigensHumansMiceMice, TransgenicSex FactorsAutoantibodiesCollagen Type IIHLA Antigens

Identifiers

PMID21665435
PMCPMC3173520
OpenAlexW2025908441

What OpenQuestion holds

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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.