Primarily Chronic Progressive and Relapsing/Remitting Multiple Sclerosis: Two Immunogenetically Distinct Disease Entities

• Published in: Proceedings of the National Academy of Sciences - PNAS 1989-09, Vol.86 (18), p.7113-7117
• Main Authors: Olerup, Olle, Hillert, Jan, Fredrikson, Sten, Olsson, Tomas, Kam-Hansen, Slavenka, Möller, Erna, Carlsson, Björn, Wallin, Johan
• Format: Article
• Language: English
• Subjects: Alleles; Antigens; Biological and medical sciences; Central nervous system viral diseases; Chronic diseases; Deoxyribonucleases, Type II Site-Specific; DNA; Epidemiology; Fundamental and applied biological sciences. Psychology; Fundamental immunology; Genes, MHC Class II; Genetic loci; Haplotypes; Histocompatibility antigens (hla, h-2 and other systems); Histocompatibility Antigens Class II - analysis; Histocompatibility Antigens Class II - genetics; HLA antigens; Humans; Molecular immunology; Multiple sclerosis; Multiple Sclerosis - classification; Multiple Sclerosis - genetics; Multiple Sclerosis - immunology; Nervous system diseases; Polymorphism, Genetic; Polymorphism, Restriction Fragment Length; Recurrence; Reference Values; Remission, Spontaneous; Sweden
• ISSN: 0027-8424; 1091-6490
• DOI: 10.1073/pnas.86.18.7113

HLA class II gene polymorphism was investigated in 100 patients with clinically definite multiple sclerosis (MS) by restriction fragment length polymorphism analysis of Taq I-digested DNA using DRB, DQA, and DQB cDNA probes. Twenty-six patients had primarily chronic progressive MS and 74 had relapsing/remitting MS. The latter group included patients with a secondary progressive evolution of symptoms. Both clinical forms of MS were found to be associated with the DRw15, DQw6 haplotype. In addition, primarily chronic progressive MS was positively associated with the DQB1 restriction fragment pattern seen in DR4, DQw8, DR7, DQw9, and DRw8, DQw4 haplotypes, as well as negatively associated with the Taq I DQB1 allelic pattern corresponding to the serological specificity DQw7. Relapsing/remitting MS was positively associated with the DQB1 allelic pattern observed in the DRw17, DQw2 haplotype. These three DQB1 alleles are in strong negative linkage disequilibria with DRw15. The two susceptibility markers of each clinical form of MS act additively in determining the genetic susceptibility, as the relative risks for individuals carrying both markers roughly equal the sum of respective risks. Different alleles of the DQB1 locus defined by restriction fragment length polymorphisms contribute to susceptibility and resistance to primarily chronic progressive MS as well as to susceptibility to relapsing/remitting MS. The observed immunogenetic heterogeneity between the different clinical forms of MS favors the hypothesis that primarily chronic progressive MS and relapsing/remitting MS are two distinct disease entities.