Intercellular adhesion molecule-1:: a protective haplotype against multiple sclerosis

被引:28
作者
Cournu-Rebeix, I
Génin, E
Lesca, G
Azoulay-Cayla, A
Tubridy, N
Noé, E
Clanet, M
Edan, G
Clerget-Darpoux, F
Sémana, G
Fontaine, B
机构
[1] Univ Paris 06, Lab Affect Myeline & Canaux Ion Musculaires, INSERM, U546, F-75013 Paris, France
[2] Ctr Hosp Univ, INSERM, U535, Le Kremlin Bicetre, France
[3] Grp Hosp Pitie Salpetriere, Federat Neurol, F-75634 Paris, France
[4] Ctr Reg Hosp Univ Purpan, Serv Neurol, Toulouse, France
[5] Ctr Reg Hosp Univ Pontchaillou, Serv Neurol, Rennes, France
[6] Etab Francais Sang Bretagne, Immunogenet Lab, Rennes, France
[7] Ctr Hosp Reg Univ, Immunol Lab, UPRES EA 1257, Rennes, France
[8] Fac Med, Rennes, France
关键词
multiple sclerosis; intercellular adhesion molecule-1; haplotypes; association; transmission disequilibrium test; receptors;
D O I
10.1038/sj.gene.6364009
中图分类号
Q3 [遗传学];
学科分类号
071007 ; 090102 ;
摘要
Intercellular adhesion molecule-1 (ICAM-1) and its receptors are adhesion molecules that play a key role in the transmigration of inflammatory cells through the blood-brain barrier, one of the earliest events in multiple sclerosis (MS), which leads to demyelination in the central nervous system. To investigate the role of genes encoding ICAM-1 and its receptors, we used a strategy of genetic linkage and association in 439 case-parent MS families of French origin, well characterized according to HLA status and severity. We demonstrate that the genes encoding ICAM-1 receptors do not influence MS susceptibility or severity. ICAM-1 had a modest, but significant effect on MS genetic susceptibility, independent of HLA and disease severity. We observed a rare, and an as yet unreported, ICAM-1 gene haplotype defined by amino acids K469 and R241 that was never transmitted to patients suggesting a protective effect against MS in our population.
引用
收藏
页码:518 / 523
页数:6
相关论文
共 43 条
[1]   Haplotypes vs single marker linkage disequilibrium tests:: what do we gain? (Reprinted European Journal of Human Genetics, Vol 4, pg 291-300, 2001) [J].
Akey, Joshua ;
Jin, Li ;
Xiong, Momiao .
EUROPEAN JOURNAL OF HUMAN GENETICS, 2017, 25 :S51-S58
[2]  
ALPEROVITCH A, 1995, MED THERAPEUTIQUE, V1, P545
[3]   Familial factors influence disability in MS multiplex families [J].
Brassat, D ;
Azais-Vuillemin, C ;
Yaouanq, J ;
Semana, G ;
Reboul, J ;
Cournu, I ;
Mertens, C ;
Edan, G ;
Lyon-Caen, O ;
Clanet, C ;
Fontaine, B .
NEUROLOGY, 1999, 52 (08) :1632-1636
[4]   UP-REGULATION AND COEXPRESSION OF ADHESION MOLECULES CORRELATE WITH RELAPSING AUTOIMMUNE DEMYELINATION IN THE CENTRAL-NERVOUS-SYSTEM [J].
CANNELLA, B ;
CROSS, AH ;
RAINE, CS .
JOURNAL OF EXPERIMENTAL MEDICINE, 1990, 172 (05) :1521-1524
[5]   BINDING OF THE INTEGRIN MAC-1 (CD11B/CD18) TO THE 3RD IMMUNOGLOBULIN-LIKE DOMAIN OF ICAM-1 (CD54) AND ITS REGULATION BY GLYCOSYLATION [J].
DIAMOND, MS ;
STAUNTON, DE ;
MARLIN, SD ;
SPRINGER, TA .
CELL, 1991, 65 (06) :961-971
[6]   Experimentally-derived haplotypes substantially increase the efficiency of linkage disequilibrium studies [J].
Douglas, JA ;
Boehnke, M ;
Gillanders, E ;
Trent, JA ;
Gruber, SB .
NATURE GENETICS, 2001, 28 (04) :361-364
[7]   Genetic analysis of case/control data using estimated haplotype frequencies: Application to APOE locus variation and Alzheimer's disease [J].
Fallin, D ;
Cohen, A ;
Essioux, L ;
Chumakov, I ;
Blumenfeld, M ;
Cohen, D ;
Schork, NJ .
GENOME RESEARCH, 2001, 11 (01) :143-151
[8]   DIAGNOSTIC-CRITERIA FOR MULTIPLE-SCLEROSIS RESEARCH INVOLVING MULTIPLY AFFECTED FAMILIES [J].
GOODKIN, DE ;
DOOLITTLE, TH ;
HAUSER, SS ;
RANSOHOFF, RM ;
ROSES, AD ;
RUDICK, RA .
ARCHIVES OF NEUROLOGY, 1991, 48 (08) :805-807
[9]  
GREENWOOD J, 1995, IMMUNOLOGY, V86, P408
[10]   THE MAJOR HUMAN RHINOVIRUS RECEPTOR IS ICAM-1 [J].
GREVE, JM ;
DAVIS, G ;
MEYER, AM ;
FORTE, CP ;
YOST, SC ;
MARIOR, CW ;
KAMARCK, ME ;
MCCLELLAND, A .
CELL, 1989, 56 (05) :839-847