Evidence map›Paper›PMID 8016129›Full record

ArticleProceedings of the National Academy of Sciences of the United States of America1994

Expression of HLA-DR4 and human CD4 transgenes in mice determines the variable region beta-chain T-cell repertoire and mediates an HLA-DR-restricted immune response.

L Fugger, S A Michie, I Rulifson, C B Lock, G S McDevitt

Open access · greenAbstract readComparative Study
In one paragraph

Article in Proceedings of the National Academy of Sciences of the United States of America, 1994. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 35 papers.

0numbers the graph read from it
0cells of the map it votes in
35citing papers in PubMed
0.9field-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

35 citing papers in PubMed, 89 citations in OpenAlex.

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  9. A humanized HLA-DR4 mouse model for autoimmune myocarditis.Journal of molecular and cellular cardiology · 2017
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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.

L FuggerDepartment of Microbiology, Stanford University School of Medicine, CA 94305.
S A Michie
I Rulifson
C B Lock
G S McDevitt
Stanford University · US

Funding

STRUCTURE/FUNCTION OF CLASS II MHC MOLECULESR35CA049734 · NCI · STANFORD UNIVERSITY · PI MCDEVITT, HUGH O · 1989 to 1995
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NCI NIH HHS CA 49734
6 · The paper itself

Abstract

Inherited susceptibility to rheumatoid arthritis is associated with genes encoding the human major histocompatibility complex class II molecule HLA-DR4. To study the immune function of HLA-DR4 and attempt to generate a murine model of rheumatoid arthritis we have produced triple transgenic mice expressing HLA-DRA*0101, -DRB1*0401, and human CD4. The expression of the HLA transgenes is driven by the promoter of the murine major histocompatibility complex class II I-E alpha gene and was found on murine cells that normally display major histocompatibility complex class II molecules. The expression of the human CD4 transgene is driven by the murine CD3 delta-promoter, and therefore its gene product was found on cells that express murine CD3. In contrast to other HLA-DR and HLA-DQ transgenic mouse lines, the transgenes are functional in our mice. In H-2 I-E-negative transgenic mice, T cells expressing variable region beta chain (V beta) 3, 5, 6, 7, 9, 11, 12, or 13 were either absent or significantly reduced, in contrast to H-2 I-E-negative nontransgenic littermates. In addition, the peptide antigen influenza A virus hemagglutinin 307-319, which binds to the HLA-DRA*0101/-DRB1*0401 heterodimer with high affinity and induces an HLA-DR-restricted and CD4+ T-cell response in humans, also induced a T-cell response in the triple transgenic mice but not in nontransgenic littermates. Thus, these transgenic mice should permit extensive testing of the antigen-presentation capabilities of the HLA-DRA*0101/-DRB1*0401 molecule.

Indexed as

AnimalsAntibodies, MonoclonalAntigens, CDArthritis, ExperimentalArthritis, RheumatoidCD3 ComplexCD4 AntigensDisease SusceptibilityFemaleFlow CytometryGenetic Predisposition to DiseaseGenetic VariationHLA-DQ AntigensHLA-DR4 AntigenHLA-DR AntigensHumansAntibodies, MonoclonalAntigens, CDCD3 ComplexCD4 AntigensHLA-DQ AntigensHLA-DR4 AntigenHLA-DR AntigensReceptors, Antigen, T-Cell, alpha-beta

Identifiers

PMID8016129
PMCPMC44156
OpenAlexW2047150609

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.