Volume 11, Issue 4 819041 pp. 191-203
Article
Open Access

Association of the HLA-A2, CW2, B27, S31, DR2 Haplotype with Ankylosing Spondylitis. A Possible Role of NON-B27 Factors in the Disease

Giorgio La Nasa

Giorgio La Nasa

The Department of Medical Genetics of the Institute of Clinical Medicine University of Cagliari Cagliari, Italy

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Alessandro Mathleu

Alessandro Mathleu

The Department of Medical Genetics and the Department of Rheumatology II of the Institute ofClinical Medicine University of Cagliari Cagliari, Italy

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Marina Mulargia

Marina Mulargia

The Department of Medical Genetics of the Institute of Clinical Medicine University of Cagliari Cagliari, Italy

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Carlo Carcassi

Corresponding Author

Carlo Carcassi

The Department of Medical Genetics of the Institute of Clinical Medicine University of Cagliari Cagliari, Italy

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Adriana Vacca

Adriana Vacca

The Department of Medical Genetics of the Institute of Clinical Medicine University of Cagliari Cagliari, Italy

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Antonio Ledda

Antonio Ledda

The Department of Medical Genetics of the Institute of Clinical Medicine University of Cagliari Cagliari, Italy

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Licinio Contu

Corresponding Author

Licinio Contu

The Department of Medical Genetics of the Institute of Clinical Medicine University of Cagliari Cagliari, Italy

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First published: 01 January 1993
Citations: 9

Abstract

With the aim of searching for HLA haplotypes and non-B27 allele frequency variations in Sardinian AS patients, HLA-A, B, Cw, DR, DQ and Bf, C4A and C4B typing and haplotype assignment was carried out in the families of 25 AS patients and in 44 healthy individuals, all B27 heterozygotes. In the AS patients a significant increase of the A2, Cw2, B27, DR2, DQ1 haplotype was found. This depends only partially on the linkage disequilibrium existing in the Sardinian population between B27 and the other alleles of this haplotype, and rather seems to be due to a primary association of Cw2 and DR2 alleles with AS. Preliminary data seem to show that this haplotype bears the S3l complotype and the ORB1 * 1601 allele both in the AS patients and in the healthy controls. The pathogenetic implications of these findings are discussed.

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