DIFFERENTIAL CONTRIBUTION OF HLA-DR, DQ, AND TAP2 ALLELES TO SYSTEMICLUPUS-ERYTHEMATOSUS SUSCEPTIBILITY IN SPANISH PATIENTS - ROLE OF TAP2-ASTERISK-01 ALLELES IN RO AUTOANTIBODY PRODUCTION

Citation
Jm. Martinvilla et al., DIFFERENTIAL CONTRIBUTION OF HLA-DR, DQ, AND TAP2 ALLELES TO SYSTEMICLUPUS-ERYTHEMATOSUS SUSCEPTIBILITY IN SPANISH PATIENTS - ROLE OF TAP2-ASTERISK-01 ALLELES IN RO AUTOANTIBODY PRODUCTION, Annals of the Rheumatic Diseases, 57(4), 1998, pp. 214-219
Citations number
29
Categorie Soggetti
Rheumatology
ISSN journal
00034967
Volume
57
Issue
4
Year of publication
1998
Pages
214 - 219
Database
ISI
SICI code
0003-4967(1998)57:4<214:DCOHDA>2.0.ZU;2-6
Abstract
Objective-To study the influence MHC class II and TAP2 alleles exert o n systemic lupus erythematosus (SLE) susceptibility and on the clinica l and serological manifestations of the disease, in a cohort of Spanis h patients. Methods-HLA-DR serological typing and HLA-DQA, DQB, and TA P2 DNA sequence specific oligotyping, were carried out in 85 unrelated Spanish SLE patients and 186 healthy controls. Autoantibodies detecti on was carried out by indirect immunofluorescence and counter immune e lectrophoresis. Results-Total SLE group: the frequency of HLA-DR3 and HLA-DQA1 star 0501 is significantly increased in this group (p(c)<0.00 5, delta=0.34 and p(c)<0.005, delta= 0.45, respectively) although the highest delta value (delta=0.87) is obtained when the TAP2 star 01 all eles are considered. No DQB allele shows significant deviation from th e control group. Renal damage: it mainly occurs in HLA-DR3 patients (p (c)<0.0005 and delta=0.72). HLA-DQA1 star 0501 (p(c)<0.05, delta=0.57) and DQB1 star 0201 (p(c) NS, delta=0.56) are weaker susceptibility fa ctors. Ro+ (but not La) group: this autoantibody response is associate d with TAP2 star 01 alleles in homozygosity (p<0.05, delta=0.81). Ro/L a+ group: it has a different genetic background as HLA-DQA1 star 0501 (delta=1) and HLA-DQB1 star 0201 (delta=1) are the main susceptibility factors. Conclusions-A differential association between HLA-DR, DQA1, and DQB1 alleles and SLE or its clinical and serological manifestatio ns are found. Furthermore, the associations are different to the ones reported in other ethnic groups. Finally, TAP2 star 01 group of allele s are associated with the highest susceptibility to SLE (higher than H LA-DR3) and may influence Ho (but not La) autoantibodies production, w hereas HLA-DQA1 star 0501 and DQB1 star 0201 mediates concomitant Ro a nd La production.