Evidence map›Paper›PMID 21964024›Full record

ArticleJournal of immunology (Baltimore, Md. : 1950)2011

MHC class I family proteins retard systemic lupus erythematosus autoimmunity and B cell lymphomagenesis.

Caroline G McPhee, Thomas J Sproule, Dong-Mi Shin, Jason A Bubier, William H Schott, Martin P Steinbuck, Lia Avenesyan, Herbert C Morse, Derry C Roopenian

Open access · bronzeAbstract read
In one paragraph

Article in Journal of immunology (Baltimore, Md. : 1950), 2011. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 29 papers.

0numbers the graph read from it
0cells of the map it votes in
29citing papers in PubMed
1.0field-weighted citation impact, top 25% 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

29 citing papers in PubMed, 43 citations in OpenAlex.

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  17. Non-pathogenic tissue-resident CD8Scientific reports · 2017
    Article
  18. Article
  19. Transgenic mouse model of IgMBlood cancer journal · 2016
    Article
  20. 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

9 authors at 3 institutions in 1 country.

Caroline G McPheeThe Jackson Laboratory, Bar Harbor, ME 04609, USA.
Thomas J Sproule
Dong-Mi Shin
Jason A Bubier
William H Schott
Martin P Steinbuck
Lia Avenesyan
Herbert C Morse
Derry C Roopenian
Jackson Laboratory · USNational Institute of Allergy and Infectious Diseases · USNational Institutes of Health · US

Funding

Molecular Regulation of B-Cell Differentiation and FunctionZIAAI001024 · NIAID · NATIONAL INSTITUTE OF ALLERGY AND INFECTIOUS DISEASES · PI MORSE, HERBERT · 2009 to 2018
$8.3M
Lymphomas And Retroviral PathogenesisZIAAI000858 · NIAID · NATIONAL INSTITUTE OF ALLERGY AND INFECTIOUS DISEASES · PI MORSE, HERBERT · 2009 to 2018
$5.3M
Molecular Mechanisms in Innate immunityZIAAI001057 · NIAID · NATIONAL INSTITUTE OF ALLERGY AND INFECTIOUS DISEASES · PI MORSE, HERBERT · 2009 to 2018
$4.7M
CLASS I MOLECULES AND AUTOIMMUNITYR01DK056597 · NIDDK · JACKSON LABORATORY · PI ROOPENIAN, DERRY CHARLES · 1999 to 2006
$2.4M
Characterization of Y-linked Autoimmune Accelerator YaaR21DK074463 · NIDDK · JACKSON LABORATORY · PI ROOPENIAN, DERRY CHARLES · 2006 to 2007
$456k
Intramural NIH HHS ZIA AI001057NIDDK NIH HHS R01 DK056597NIDDK NIH HHS R21 DK074463
6 · The paper itself

Abstract

Dysregulation of the T cell-dependent Ab response can lead to numerous immunological disorders, ranging from systemic lupus erythematosus to B cell lymphomas. Cellular processes governed by MHC class II proteins play a major role in this response and its dysregulation. The extent to which processes controlled by the diverse family of MHC class I proteins impact such autoimmune and neoplastic disorders, however, is less clear. In this study, we genetically dissect the contributions of individual MHC class I family members and the pathological processes under their control in the systemic lupus erythematosus-like disease of BXSB.Yaa mice and B cell lymphomagenesis of SJL mice. This study reveals a powerful repressive regulatory axis comprised of MHC class I-dependent CD8(+) T cells and NK cells. These results indicate that the predominant role of the MHC class I protein family in such immunological disorders is to protect from more aggressive diseases.

Indexed as

Animalsbeta 2-MicroglobulinB-Lymphocyte SubsetsCD4-Positive T-LymphocytesCD8-Positive T-LymphocytesH-2 AntigensHistocompatibility Antigen H-2DHistocompatibility Antigens Class IKiller Cells, NaturalLupus Erythematosus, SystemicLymphoma, B-CellMiceMice, Inbred StrainsMoloney murine leukemia virusbeta 2-MicroglobulinH-2 AntigensH-2K(K) antigenHistocompatibility Antigen H-2DHistocompatibility Antigens Class I

Identifiers

PMID21964024
PMCPMC3381364
OpenAlexW2169554269

What OpenQuestion holds

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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.