Current gene-mapping strategies in experimental models of multiple sclerosis

被引:9
作者
Becanovic, K [1 ]
Jagodic, M [1 ]
Wallström, E [1 ]
Olsson, T [1 ]
机构
[1] Karolinska Inst, Neuroimmunol Unit, Sect Neurosci Res, Dept Clin Neurosci,CMM, SE-17176 Stockholm, Sweden
关键词
D O I
10.1111/j.0300-9475.2004.01462.x
中图分类号
R392 [医学免疫学]; Q939.91 [免疫学];
学科分类号
100102 ;
摘要
Both family-based linkage analyses and population-based association studies have failed to identify disease-regulatory non-human leucocyte antigen genes of importance in multiple sclerosis (MS). Instead, investigators have employed experimental models, which offer major advantages in genetic studies. We summarize the current main methodologies used and the status of both the human and experimental approaches. Why is it important to find genes regulating MS? There is an immense number of cellular and molecular interactions defined in the immunological field and it is very difficult to unravel those that are critical to an inflammatory disease, such as MS, by classical hypothesis-driven research. Unbiased genetics defines evolutionary conserved gene polymorphisms and pathways regulated by these genes, which are central in the pathogenesis. These, in turn, are of interest as therapeutic targets and pharmacogenetic markers.
引用
收藏
页码:39 / 51
页数:13
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共 105 条
[11]  
Berger T, 1997, LAB INVEST, V76, P355
[12]   Evidence for common autoimmune disease genes controlling onset, severity, and chronicity based on experimental models for multiple sclerosis and rheumatoid arthritis [J].
Bergsteinsdottir, K ;
Yang, HT ;
Pettersson, U ;
Holmdahl, R .
JOURNAL OF IMMUNOLOGY, 2000, 164 (03) :1564-1568
[13]   Genetic analysis of the influence of pertussis toxin on experimental allergic encephalomyelitis susceptibility: An environmental agent can override genetic checkpoints [J].
Blankenhorn, EP ;
Butterfield, RJ ;
Rigby, R ;
Cort, L ;
Giambrone, D ;
McDermott, P ;
McEntee, K ;
Solowski, N ;
Meeker, ND ;
Zachary, JF ;
Doerge, RW ;
Teuscher, C .
JOURNAL OF IMMUNOLOGY, 2000, 164 (06) :3420-3425
[14]   A genome screen for multiple sclerosis in Italian families [J].
Broadley, S ;
Sawcer, S ;
D'Alfonso, S ;
Hensiek, A ;
Coraddu, F ;
Gray, J ;
Roxburgh, R ;
Clayton, D ;
Buttinelli, C ;
Quattrone, A ;
Trojano, M ;
Massacesi, L ;
Compston, A .
GENES AND IMMUNITY, 2001, 2 (04) :205-210
[15]  
Butterfield RJ, 1998, J IMMUNOL, V161, P1860
[16]  
Butterfield RJ, 1999, J IMMUNOL, V162, P3096
[17]   Identification of genetic loci controlling the characteristics and severity of brain and spinal cord lesions in experimental allergic encephalomyelitis [J].
Butterfield, RJ ;
Blankenhorn, EP ;
Roper, RJ ;
Zachary, JF ;
Doerge, RW ;
Teuscher, G .
AMERICAN JOURNAL OF PATHOLOGY, 2000, 157 (02) :637-645
[18]   PLAQUE-ASSOCIATED EXPRESSION OF HUMAN HERPESVIRUS-6 IN MULTIPLE-SCLEROSIS [J].
CHALLONER, PB ;
SMITH, KT ;
PARKER, JD ;
MACLEOD, DL ;
COULTER, SN ;
ROSE, TM ;
SCHULTZ, ER ;
BENNETT, JL ;
GARBER, RL ;
CHANG, M ;
SCHAD, PA ;
SEWART, PM ;
NOWINSKI, RC ;
BROWN, JP ;
BURMER, GC .
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 1995, 92 (16) :7440-7444
[19]   The genetics of multiple sclerosis: principles, background and updated results of the United Kingdom systematic genome screen [J].
Chataway, J ;
Feakes, R ;
Coraddu, F ;
Gray, J ;
Deans, J ;
Fraser, M ;
Robertson, N ;
Broadley, S ;
Jones, H ;
Clayton, D ;
Goodfellow, P ;
Sawcer, S ;
Compston, A .
BRAIN, 1998, 121 :1869-1887
[20]  
CHURCHILL GA, 1994, GENETICS, V138, P963