Association of rheumatoid arthritis with an amino acid allelic variation of the T cell receptor.

OBJECTIVE: To investigate allelic variations of T cell receptor residues for a contribution to rheumatoid arthritis (RA) susceptibility. METHODS: We conducted an RA case-control study involving 1,579 northwest Europeans: 766 patients with erosive and rheumatoid factor-positive disease and 813 contro...

Full description

Bibliographic Details
Main Authors: Cornélis, F, Hardwick, L, Flipo, R, Martinez, M, Lasbleiz, S, Prud'homme, J, Tran, T, Walsh, S, Delaye, A, Nicod, A, Loste, M, Lepage, V, Gibson, K, Pile, K, Djoulah, S, Danzé, P, Lioté, F, Charron, D, Weissenbach, J, Kuntz, D, Bardin, T, Wordsworth, B
Format: Conference item
Published: 1997
_version_ 1797060355296329728
author Cornélis, F
Hardwick, L
Flipo, R
Martinez, M
Lasbleiz, S
Prud'homme, J
Tran, T
Walsh, S
Delaye, A
Nicod, A
Loste, M
Lepage, V
Gibson, K
Pile, K
Djoulah, S
Danzé, P
Lioté, F
Charron, D
Weissenbach, J
Kuntz, D
Bardin, T
Wordsworth, B
author_facet Cornélis, F
Hardwick, L
Flipo, R
Martinez, M
Lasbleiz, S
Prud'homme, J
Tran, T
Walsh, S
Delaye, A
Nicod, A
Loste, M
Lepage, V
Gibson, K
Pile, K
Djoulah, S
Danzé, P
Lioté, F
Charron, D
Weissenbach, J
Kuntz, D
Bardin, T
Wordsworth, B
author_sort Cornélis, F
collection OXFORD
description OBJECTIVE: To investigate allelic variations of T cell receptor residues for a contribution to rheumatoid arthritis (RA) susceptibility. METHODS: We conducted an RA case-control study involving 1,579 northwest Europeans: 766 patients with erosive and rheumatoid factor-positive disease and 813 control subjects. Productive changes of segments TCRAV6S1, TCRAV7S1, TCRAV8S1, TCRAV10S2, and TCRBV6S1, TCRBV6S7 were investigated by single-strand conformation polymorphisms. The TCRAV8S1 association was confirmed by restriction fragment length polymorphism. RESULTS: In the systematic study (77 patients and 119 controls), an increase in 1 TCRAV8S1 genotype was found in the RA patients (P = 0.0004). This finding was replicated in 2 further populations, one from France (212 patients and 254 controls) and the other from Britain (477 patients and 440 controls), with a similar odds ratio (OR), which allowed pooling of the data and confirmation of the association (OR 1.3 [95% confidence interval 1.1-1.7], P = 0.008). CONCLUSION: These findings show evidence that TCRA is an RA susceptibility locus.
first_indexed 2024-03-06T20:15:56Z
format Conference item
id oxford-uuid:2c25af78-bcc8-498a-bd08-73ded551f070
institution University of Oxford
last_indexed 2024-03-06T20:15:56Z
publishDate 1997
record_format dspace
spelling oxford-uuid:2c25af78-bcc8-498a-bd08-73ded551f0702022-03-26T12:35:16ZAssociation of rheumatoid arthritis with an amino acid allelic variation of the T cell receptor.Conference itemhttp://purl.org/coar/resource_type/c_5794uuid:2c25af78-bcc8-498a-bd08-73ded551f070Symplectic Elements at Oxford1997Cornélis, FHardwick, LFlipo, RMartinez, MLasbleiz, SPrud'homme, JTran, TWalsh, SDelaye, ANicod, ALoste, MLepage, VGibson, KPile, KDjoulah, SDanzé, PLioté, FCharron, DWeissenbach, JKuntz, DBardin, TWordsworth, BOBJECTIVE: To investigate allelic variations of T cell receptor residues for a contribution to rheumatoid arthritis (RA) susceptibility. METHODS: We conducted an RA case-control study involving 1,579 northwest Europeans: 766 patients with erosive and rheumatoid factor-positive disease and 813 control subjects. Productive changes of segments TCRAV6S1, TCRAV7S1, TCRAV8S1, TCRAV10S2, and TCRBV6S1, TCRBV6S7 were investigated by single-strand conformation polymorphisms. The TCRAV8S1 association was confirmed by restriction fragment length polymorphism. RESULTS: In the systematic study (77 patients and 119 controls), an increase in 1 TCRAV8S1 genotype was found in the RA patients (P = 0.0004). This finding was replicated in 2 further populations, one from France (212 patients and 254 controls) and the other from Britain (477 patients and 440 controls), with a similar odds ratio (OR), which allowed pooling of the data and confirmation of the association (OR 1.3 [95% confidence interval 1.1-1.7], P = 0.008). CONCLUSION: These findings show evidence that TCRA is an RA susceptibility locus.
spellingShingle Cornélis, F
Hardwick, L
Flipo, R
Martinez, M
Lasbleiz, S
Prud'homme, J
Tran, T
Walsh, S
Delaye, A
Nicod, A
Loste, M
Lepage, V
Gibson, K
Pile, K
Djoulah, S
Danzé, P
Lioté, F
Charron, D
Weissenbach, J
Kuntz, D
Bardin, T
Wordsworth, B
Association of rheumatoid arthritis with an amino acid allelic variation of the T cell receptor.
title Association of rheumatoid arthritis with an amino acid allelic variation of the T cell receptor.
title_full Association of rheumatoid arthritis with an amino acid allelic variation of the T cell receptor.
title_fullStr Association of rheumatoid arthritis with an amino acid allelic variation of the T cell receptor.
title_full_unstemmed Association of rheumatoid arthritis with an amino acid allelic variation of the T cell receptor.
title_short Association of rheumatoid arthritis with an amino acid allelic variation of the T cell receptor.
title_sort association of rheumatoid arthritis with an amino acid allelic variation of the t cell receptor
work_keys_str_mv AT cornelisf associationofrheumatoidarthritiswithanaminoacidallelicvariationofthetcellreceptor
AT hardwickl associationofrheumatoidarthritiswithanaminoacidallelicvariationofthetcellreceptor
AT flipor associationofrheumatoidarthritiswithanaminoacidallelicvariationofthetcellreceptor
AT martinezm associationofrheumatoidarthritiswithanaminoacidallelicvariationofthetcellreceptor
AT lasbleizs associationofrheumatoidarthritiswithanaminoacidallelicvariationofthetcellreceptor
AT prudhommej associationofrheumatoidarthritiswithanaminoacidallelicvariationofthetcellreceptor
AT trant associationofrheumatoidarthritiswithanaminoacidallelicvariationofthetcellreceptor
AT walshs associationofrheumatoidarthritiswithanaminoacidallelicvariationofthetcellreceptor
AT delayea associationofrheumatoidarthritiswithanaminoacidallelicvariationofthetcellreceptor
AT nicoda associationofrheumatoidarthritiswithanaminoacidallelicvariationofthetcellreceptor
AT lostem associationofrheumatoidarthritiswithanaminoacidallelicvariationofthetcellreceptor
AT lepagev associationofrheumatoidarthritiswithanaminoacidallelicvariationofthetcellreceptor
AT gibsonk associationofrheumatoidarthritiswithanaminoacidallelicvariationofthetcellreceptor
AT pilek associationofrheumatoidarthritiswithanaminoacidallelicvariationofthetcellreceptor
AT djoulahs associationofrheumatoidarthritiswithanaminoacidallelicvariationofthetcellreceptor
AT danzep associationofrheumatoidarthritiswithanaminoacidallelicvariationofthetcellreceptor
AT liotef associationofrheumatoidarthritiswithanaminoacidallelicvariationofthetcellreceptor
AT charrond associationofrheumatoidarthritiswithanaminoacidallelicvariationofthetcellreceptor
AT weissenbachj associationofrheumatoidarthritiswithanaminoacidallelicvariationofthetcellreceptor
AT kuntzd associationofrheumatoidarthritiswithanaminoacidallelicvariationofthetcellreceptor
AT bardint associationofrheumatoidarthritiswithanaminoacidallelicvariationofthetcellreceptor
AT wordsworthb associationofrheumatoidarthritiswithanaminoacidallelicvariationofthetcellreceptor