THE HLA-DW2 HAPLOTYPE SEGREGATES CLOSELY WITH MULTIPLE-SCLEROSIS IN MULTIPLEX FAMILIES

被引:40
作者
HILLERT, J
KALL, T
VRETHEM, M
FREDRIKSON, S
OHLSON, M
OLERUP, O
机构
[1] HUDDINGE HOSP,KAROLINSKA INST,DEPT NEUROL,HUDDINGE,SWEDEN
[2] HUDDINGE HOSP,KAROLINSKA INST,DEPT CLIN IMMUNOL,HUDDINGE,SWEDEN
[3] LINKOPING UNIV HOSP,DEPT NEUROL,S-58185 LINKOPING,SWEDEN
[4] UNIV HOSP UPPSALA,DEPT NEUROL,S-75185 UPPSALA,SWEDEN
关键词
FAMILIAR DISEASE; GENETIC SUSCEPTIBILITY; HLA ANTIGENS; HLA HAPLOTYPE; MULTIPLE SCLEROSIS;
D O I
10.1016/0165-5728(94)90219-4
中图分类号
R392 [医学免疫学]; Q939.91 [免疫学];
学科分类号
100102 ;
摘要
Multiple sclerosis (MS) is associated with the HLA class II specificity Dw2, but the importance of its influence has been questioned, since sib-pair analysis has failed to show linkage with this haplotype. However, the use of 'identity by descent' (IBD) analysis may not be ideal, since it does not make use of the facts that (i) the Dw2-haplotype is the only haplotype with a confirmed role in MS, and (ii) it performs its influence in a dominant manner. We have investigated nine Swedish multiplex MS families. In eight of the families, the Dw2 haplotype occurred in MS patients. Within these families, Dw2 was shared by all 17 individuals with MS. In a compilation of 48 published multiplex MS families in which at least one patient carried Dw2, only three of 107 individuals with MS did not carry the Dw2 haplotype. This indicates that the Dw2 haplotype, when present in familial MS, may confer a stronger influence in MS susceptibility than generally recognized.
引用
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页码:95 / 100
页数:6
相关论文
共 50 条
[1]  
ALDIN ASN, 1986, TISSUE ANTIGENS, V27, P196
[2]  
ALPEROVITCH A, 1992, ANN NEUROL, V32, P724
[3]   THE GERMLINE REPERTOIRE OF T-CELL RECEPTOR BETA-CHAIN GENES IN PATIENTS WITH CHRONIC PROGRESSIVE MULTIPLE-SCLEROSIS [J].
BEALL, SS ;
CONCANNON, P ;
CHARMLEY, P ;
MCFARLAND, HF ;
GATTI, RA ;
HOOD, LE ;
MCFARLIN, DE ;
BIDDISON, WE .
JOURNAL OF NEUROIMMUNOLOGY, 1989, 21 (01) :59-66
[4]   DNA LENGTH POLYMORPHISM-5' TO THE MYELIN BASIC-PROTEIN GENE IS ASSOCIATED WITH MULTIPLE-SCLEROSIS [J].
BOYLAN, KB ;
TAKAHASHI, N ;
PATY, DW ;
SADOVNICK, AD ;
DIAMOND, M ;
HOOD, LE ;
PRUSINER, SB .
ANNALS OF NEUROLOGY, 1990, 27 (03) :291-297
[5]   HLA-DR-DQ HAPLOTYPES DEFINED BY RESTRICTION FRAGMENT ANALYSIS - CORRELATION TO SEROLOGY [J].
CARLSSON, B ;
WALLIN, J ;
BOHME, J ;
MOLLER, E .
HUMAN IMMUNOLOGY, 1987, 20 (02) :95-113
[6]   HLA AND SUSCEPTIBILITY TO MULTIPLE-SCLEROSIS [J].
CLERGETDARPOUX, F ;
GOVAERTS, A ;
FEINGOLD, N .
TISSUE ANTIGENS, 1984, 24 (03) :160-169
[7]  
DUPONT B, 1977, TRANSPLANT P, V9, P181
[8]   THE INCREASED SUSCEPTIBILITY OF WOMEN TO MULTIPLE-SCLEROSIS [J].
DUQUETTE, P ;
PLEINES, J ;
GIRARD, M ;
CHAREST, L ;
SENECALQUEVILLON, M ;
MASSE, C .
CANADIAN JOURNAL OF NEUROLOGICAL SCIENCES, 1992, 19 (04) :466-471
[9]   A POPULATION-BASED STUDY OF MULTIPLE-SCLEROSIS IN TWINS [J].
EBERS, GC ;
BULMAN, DE ;
SADOVNICK, AD ;
PATY, DW ;
WARREN, S ;
HADER, W ;
MURRAY, TJ ;
SELAND, TP ;
DUQUETTE, P ;
GREY, T ;
NELSON, R ;
NICOLLE, M ;
BRUNET, D .
NEW ENGLAND JOURNAL OF MEDICINE, 1986, 315 (26) :1638-1642
[10]  
EBERS GC, 1982, LANCET, V10, P88