TY - JOUR
T1 - Harnessing the integrated stress response for the treatment of multiple sclerosis
AU - Way, Sharon W.
AU - Popko, Brian
N1 - Funding Information:
We thank Benjamin L Clayton and Gloria Wright for their assistance with the figures, and relevant funding sources for their support. BP has received grants from the Myelin Repair Foundation and the US National Institutes of Health ( NS34939 ). SWW received a postdoctoral fellowship from the National Multiple Sclerosis Society ( FG 1998-A-1 ).
Publisher Copyright:
© 2016 Elsevier Ltd.
PY - 2016/4/1
Y1 - 2016/4/1
N2 - Multiple sclerosis is a chronic demyelinating autoimmune disease of the CNS with no known cure. Although 12 immunomodulatory therapies exist, they have only modest effects on disease progression. The field has therefore focused on the development of alternative treatment strategies, such as enhancement of remyelination and CNS repair. Progress has been made on a third, complementary treatment approach that aims to protect oligodendrocytes-and the myelin they generate and maintain-from inflammation-mediated death by enhancing the integrated stress response. Studies in cells and in mouse models of multiple sclerosis have shown that this innate protective pathway, which maintains proteostasis, can be harnessed effectively to protect oligodendrocytes and myelin during inflammation. With one drug already in clinical development for patients with multiple sclerosis, and several potential therapies under investigation, modulation of the integrated stress response might become an important component of strategies to halt the progression of the disease.
AB - Multiple sclerosis is a chronic demyelinating autoimmune disease of the CNS with no known cure. Although 12 immunomodulatory therapies exist, they have only modest effects on disease progression. The field has therefore focused on the development of alternative treatment strategies, such as enhancement of remyelination and CNS repair. Progress has been made on a third, complementary treatment approach that aims to protect oligodendrocytes-and the myelin they generate and maintain-from inflammation-mediated death by enhancing the integrated stress response. Studies in cells and in mouse models of multiple sclerosis have shown that this innate protective pathway, which maintains proteostasis, can be harnessed effectively to protect oligodendrocytes and myelin during inflammation. With one drug already in clinical development for patients with multiple sclerosis, and several potential therapies under investigation, modulation of the integrated stress response might become an important component of strategies to halt the progression of the disease.
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U2 - 10.1016/S1474-4422(15)00381-6
DO - 10.1016/S1474-4422(15)00381-6
M3 - Review article
C2 - 26873788
AN - SCOPUS:84960480352
SN - 1474-4422
VL - 15
SP - 434
EP - 443
JO - The Lancet Neurology
JF - The Lancet Neurology
IS - 4
ER -