TY - JOUR
T1 - Dual action of glatiramer acetate (Cop-1) in the treatment of CNS autoimmune and neurodegenerative disorders
AU - Kipnis, Jonathan
AU - Schwartz, Michal
PY - 2002
Y1 - 2002
N2 - Protective autoimmunity is the body's defense mechanism against destructive self-compounds such as those commonly associated with neurodegenerative disorders. Autoimmune disease and neurodegenerative disorders can thus be viewed as two extreme manifestations of the same process. Therefore, when designing therapy, it is important to avoid an approach that will cure the one by invoking the other. One way to stop, or at least slow down, the progression of neurodegeneration without risking development of an autoimmune disease is by boosting protective autoimmunity in a well-controlled way. Copolymer 1 (Cop-1), an approved drug for the treatment of multiple sclerosis, can be used as a treatment for autoimmune diseases and as a therapeutic vaccine for neurodegenerative diseases. We propose that the protective effect of Cop-1 vaccination is obtained through a well-controlled inflammatory reaction, and that the activity of Cop-1 in driving this reaction derives from its ability to serve as a'universal antigen'by weakly activating a wide spectrum of self-reactive T cells.
AB - Protective autoimmunity is the body's defense mechanism against destructive self-compounds such as those commonly associated with neurodegenerative disorders. Autoimmune disease and neurodegenerative disorders can thus be viewed as two extreme manifestations of the same process. Therefore, when designing therapy, it is important to avoid an approach that will cure the one by invoking the other. One way to stop, or at least slow down, the progression of neurodegeneration without risking development of an autoimmune disease is by boosting protective autoimmunity in a well-controlled way. Copolymer 1 (Cop-1), an approved drug for the treatment of multiple sclerosis, can be used as a treatment for autoimmune diseases and as a therapeutic vaccine for neurodegenerative diseases. We propose that the protective effect of Cop-1 vaccination is obtained through a well-controlled inflammatory reaction, and that the activity of Cop-1 in driving this reaction derives from its ability to serve as a'universal antigen'by weakly activating a wide spectrum of self-reactive T cells.
UR - http://www.scopus.com/inward/record.url?scp=0036305222&partnerID=8YFLogxK
U2 - 10.1016/S1471-4914(02)02373-0
DO - 10.1016/S1471-4914(02)02373-0
M3 - Review article
C2 - 12114110
AN - SCOPUS:0036305222
SN - 1471-4914
VL - 8
SP - 319
EP - 323
JO - Trends in Molecular Medicine
JF - Trends in Molecular Medicine
IS - 7
ER -