HLA COMPLEMENT GENE POLYMORPHISMS IN MULTIPLE-SCLEROSIS - A STUDY ON 80 ITALIAN PATIENTS

被引:10
作者
FRANCIOTTA, D
DONDI, E
BERGAMASCHI, R
PICCOLO, G
DERIL, GVM
COSI, V
CUCCIA, M
机构
[1] UNIV PAVIA, DEPT GENET & MICROBIOL, I-27100 PAVIA, ITALY
[2] UNIV PAVIA, C MONDINO FDN, IRCCS, DIV NEUROL, I-27100 PAVIA, ITALY
关键词
MULTIPLE SCLEROSIS RESTRICTION FRAGMENT LENGTH POLYMORPHISMS; HLA CLASS III GENES; COMPLEMENT COMPONENT 4;
D O I
10.1007/BF00887817
中图分类号
R74 [神经病学与精神病学];
学科分类号
摘要
We studied C4A, C4B, and Bf complement gene polymorphisms in 80 Italian patients with multiple sclerosis (MS). We observed a significantly higher frequency of C4AQ0 allele in patients with the relapsing-remitting form of MS than in ethnically homogeneous controls. Restriction fragment length polymorphism analysis by Southern blotting of the C4/CYP21 gene complex showed that a structural gene deletion was present in 45% of patients with the C4AQ0 allele. Our data support the hypothesis that relapsing-remitting MS and primarily chronic progressive MS are immunogenetically distinct diseases; further, complement factor abnormalities typical of autoimmune diseases could influence the pathogenesis of MS.
引用
收藏
页码:64 / 68
页数:5
相关论文
共 26 条
[1]   INHERITED STRUCTURAL POLYMORPHISM OF THE 4TH COMPONENT OF HUMAN-COMPLEMENT [J].
AWDEH, ZL ;
ALPER, CA .
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA-BIOLOGICAL SCIENCES, 1980, 77 (06) :3576-3580
[2]   GENETIC-BASIS OF HUMAN-COMPLEMENT C4A DEFICIENCY - DETECTION OF A POINT MUTATION LEADING TO NONEXPRESSION [J].
BARBA, G ;
RITTNER, C ;
SCHNEIDER, PM .
JOURNAL OF CLINICAL INVESTIGATION, 1993, 91 (04) :1681-1686
[3]  
BELT KT, 1984, CELL, V36, P907
[4]   NULL ALLELES OF HUMAN COMPLEMENT-C4 - EVIDENCE FOR PSEUDOGENES AT THE C4A-LOCUS AND FOR GENE CONVERSION AT THE C4B-LOCUS [J].
BRAUN, L ;
SCHNEIDER, PM ;
GILES, CM ;
BERTRAMS, J ;
RITTNER, C .
JOURNAL OF EXPERIMENTAL MEDICINE, 1990, 171 (01) :129-140
[5]   MAPPING OF STEROID 21-HYDROXYLASE GENES ADJACENT TO COMPLEMENT COMPONENT C-4 GENES IN HLA, THE MAJOR HISTOCOMPATIBILITY COMPLEX IN MAN [J].
CARROLL, MC ;
CAMPBELL, RD ;
PORTER, RR .
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 1985, 82 (02) :521-525
[6]  
COMPSTON A, 1986, P56
[7]  
COMPSTON A, 1992, CURR OPIN NEUROL NEU, V5, P175
[8]   COURSE AND PROGNOSIS OF MULTIPLE-SCLEROSIS ASSESSED BY THE COMPUTERIZED DATA-PROCESSING OF 349 PATIENTS [J].
CONFAVREUX, C ;
AIMARD, G ;
DEVIC, M .
BRAIN, 1980, 103 (JUN) :281-300
[9]   DISEASE ASSOCIATIONS WITH COMPLOTYPES, SUPRATYPES AND HAPLOTYPES [J].
DAWKINS, RL ;
CHRISTIANSEN, FT ;
KAY, PH ;
GARLEPP, M ;
MCCLUSKEY, J ;
HOLLINGSWORTH, PN ;
ZILKO, PJ .
IMMUNOLOGICAL REVIEWS, 1983, 70 :5-22
[10]  
De Paoli F, 1987, Gene Geogr, V1, P121