The British Journal of Rheumatology, Vol 36, 941-944, Copyright © 1997 by British Society for Rheumatology
C Seidl, U Koch, T Buhleier, R Frank, B Moller, E Markert, G Koller-Wagner, E Seifried and JP Kaltwasser
The sequence polymorphism of HLA-DRB1 molecules in 84 rheumatoid arthritis
(RA) patients with early RA has been analysed to evaluate whether
particular HLA-DR alleles influence disease progression in the early stage
of the disease. Clinical data were analysed by grouping the patients
according to disease-associated haplotype combinations
(DRB1*04,04/DRB1*04,01/DRB1*04,X/DRB1*01,X) in comparison to patients who
did not carry these haplotypes (DRB1*X,X). Our results indicate that
patients with early RA who are homozygous for DRB1*04 exhibit an elevated
inflammatory activity and an increase of joint affections. In addition, the
amino acid polymorphism (QR/KRAA) at position 70-74 seems to affect the
production of rheumatoid factors. These results support the role of
HLA-DRB1 alleles in the pathogenesis of RA and indicate that patients with
particular HLA-DRB1*04 haplotype combinations may require intensified
therapeutic interventions in the early stage of the disease to prevent
disease progression.
ORIGINAL PAPERS
HLA-DRB1*04 subtypes are associated with increased inflammatory activity in early rheumatoid arthritis
Institute for Transfusion Medicine and Immunohematology, Red Cross Blood Donor Service Hessen, Frankfurt/Main, Germany.
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