WILSON, A.G., DEVRIES, N., POCIOT, F. et al. (3 more authors) (1993) An allelic polymorphism within the human tumor necrosis factor alpha promoter region is strongly associated with HLA A1, B8, and DR3 alleles. Journal of Experimental Medicine, 177 (2). pp. 557-560. ISSN 0022-1007
Abstract
The tumor necrosis factor (TNF) alpha gene lies within the class III region of the major histocompatibility complex (MHC), telomeric to the class II and centromeric to the class I region. We have recently described the first polymorphism within the human TNF-alpha locus. This is biallelic and lies within the promoter region. Frequency analysis of the TNF-alpha polymorphism, using the polymerase chain reaction and single-stranded conformational polymorphism, in HLA-typed individuals, reveals a very strong association between the uncommon TNF allele and HLA A1, B8, and DR3 alleles. This is the first association between TNF-alpha and other MHC alleles and raises the possibility that the uncommon TNF-alpha allele may contribute to the many autoimmune associations of the A1,B8,DR3 haplotype.
Metadata
Item Type: | Article |
---|---|
Authors/Creators: |
|
Copyright, Publisher and Additional Information: | © 1993 The Rockefeller University Press. Reproduced in accordance with the publisher's self-archiving policy. |
Keywords: | MAJOR HISTOCOMPATIBILITY COMPLEX; GENE-REGULATION; FACTOR-BETA; TNF-BETA; CACHECTIN; SECRETION; SEQUENCES; LEVEL |
Dates: |
|
Institution: | The University of Sheffield |
Academic Units: | The University of Sheffield > Faculty of Medicine, Dentistry and Health (Sheffield) > Department of Infection, Immunity and Cardiovascular Disease The University of Sheffield > Sheffield Teaching Hospitals |
Depositing User: | Symplectic Sheffield |
Date Deposited: | 28 Sep 2016 13:55 |
Last Modified: | 23 Jun 2023 22:02 |
Published Version: | http://dx.doi.org/10.1084/jem.177.2.557 |
Status: | Published |
Publisher: | Rockefeller University Press |
Refereed: | Yes |
Identification Number: | 10.1084/jem.177.2.557 |
Open Archives Initiative ID (OAI ID): | oai:eprints.whiterose.ac.uk:97774 |