Evidence map›Paper›PMID 20370572›Full record

ArticleAutoimmunity2010

A new site-directed transgenic rheumatoid factor mouse model demonstrates extrafollicular class switch and plasmablast formation.

Rebecca A Sweet, Sean R Christensen, Michelle L Harris, Jonathan Shupe, Jaime L Sutherland, Mark J Shlomchik

Abstract read
In one paragraph

Article in Autoimmunity, 2010. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 31 papers.

0numbers the graph read from it
0cells of the map it votes in
31citing papers in PubMed
1.4field-weighted citation impact, top 19% 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

31 citing papers in PubMed, 44 citations in OpenAlex.

  1. Trial
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  11. Loss of an IgG plasma cell checkpoint in patients with lupus.The Journal of allergy and clinical immunology · 2019
    Article
  12. Article
  13. Review
  14. B Cell-ExtrinsicJournal of immunology (Baltimore, Md. : 1950) · 2017
    Article
  15. Article
  16. Article
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  19. Review
  20. Requirement for Transcription Factor Ets1 in B Cell Tolerance to Self-Antigens.Journal of immunology (Baltimore, Md. : 1950) · 2015
    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 1 institution in 1 country.

Rebecca A SweetDepartment of Immunobiology, Yale University School of Medicine, New Haven, CT 6520-8035, USA.
Sean R Christensen
Michelle L Harris
Jonathan Shupe
Jaime L Sutherland
Mark J Shlomchik
Yale University · US

Funding

Yale Pathology Tissue Services Shared ResourceP30CA016359 · NCI · YALE UNIVERSITY · PI DAVID L RIMM · 1985 to 2026
$85.0M
TOLERANCE AND AUTOIMMUNITY IN RF TRANSGENIC MICEP01AI036529 · NIAID · YALE UNIVERSITY · PI FLAVELL, RICHARD A · 1994 to 2006
$9.4M
Activation and regulation of autoreactive B cells in health and diseaseR01AI073722 · NIAID · YALE UNIVERSITY · PI SHLOMCHIK, MARK J · 2008 to 2012
$2.6M
NCI NIH HHS CA-016359NIAID NIH HHS P01 AI036529NIAID NIH HHS P01-AI/AR36529NIAID NIH HHS R01 AI073722NIAID NIH HHS R01-AI073722
6 · The paper itself

Abstract

The AM14 rheumatoid factor (RF) transgenic (Tg) mouse has been valuable for studying how self-reactive B cells are regulated beyond central tolerance, because they remain ignorant in normal mice. AM14 B-cell activation can be studied on autoimmune-prone strains or by inducing activation with IgG2a anti-chromatin antibodies (Abs). Despite the utility of conventional Ig-Tg mice, site-directed Ig-Tg (sd-Tg) mice provide a more physiological model for B-cell responses, allowing class switch and somatic hypermutation. We report here the creation of an AM14 sd-Tg mouse and describe its phenotype on both normal and autoimmune-prone backgrounds. AM14 sd-Tg B cells develop normally but remain unactivated in the BALB/c background, even after significant aging. In contrast, in the autoimmune-prone strain MRL/lpr, AM14 sd-Tg B cells become activated and secrete large amounts of IgG RF Ab into the serum. Class-switched Ab-forming cells were found in the spleen and bone marrow. IgG RF plasmablasts were also observed in extrafollicular clusters in the spleens of aged AM14 sd-Tg MRL/lpr mice. Class switch and Ab secretion were observed additionally in AM14 sd-Tg BALB/c B cells activated in vivo using IgG2a anti-chromatin Abs. Development of IgG auto-Abs is a hallmark of severe autoimmunity and is related to pathogenesis. Using the AM14 sd-Tg, we now show that switched auto-Ab-forming cells develop robustly outside germinal centers, further confirming the extrafollicular expression of activation induced cytidine deaminase (AID). This model will allow more physiological studies of B-cell biology in the future, including memory responses marked by class switch.

Indexed as

AnimalsAutoantibodiesAutoimmunityB-LymphocytesDisease Models, AnimalFemaleFlow CytometryImmunoglobulin Class SwitchingImmunoglobulin Heavy ChainsLymphocyte ActivationMaleMiceMice, Inbred BALB CMice, Inbred MRL lprMice, TransgenicMutagenesis, Site-DirectedAutoantibodiesImmunoglobulin Heavy ChainsRheumatoid Factor

Identifiers

PMID20370572
PMCPMC3818904
OpenAlexW1996071483

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.