The British Journal of Rheumatology, Vol 37, 1203-1206, Copyright © 1998 by British Society for Rheumatology
J Tuokko, S Koskinen, P Westman, U Yli-Kerttula, A Toivanen and J Ilonen
The purpose was to study tumour necrosis factor (TNF)-a, -b and -c
microsatellites as potential new susceptibility markers for reactive
arthritis (ReA). Fifty-nine patients typed for HLA-B27 were studied for
frequencies of TNF microsatellite alleles and compared with allele
frequencies determined from 285 random haplotypes and 46 healthy HLA-
B27-positive controls. TNFa, -b and -c microsatellite sequences were
amplified by the polymerase chain reaction, and the size of the product was
defined by an automated sequencer. The frequencies of TNFa6 and -c1 alleles
were found to be increased in patients with ReA, whereas TNFa11 and -c2
frequencies were decreased as compared to control haplotypes. The increase
in the c1 allele in patients with ReA independently from HLA-B27 suggests
that it might be a new susceptibility marker for the disease. The
association of ReA with other alleles was due to a linkage disequilibrium
with HLA-B27.
ORIGINAL PAPERS
Tumour necrosis factor microsatellites in reactive arthritis
Turku Immunology Centre and Department of Medical Microbiology, University of Turku, Finland.
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