TY - JOUR
T1 - Sex-dependent treatment of chronic EAE with partial MHC class II constructs
AU - Benedek, Gil
AU - Chaudhary, Priya
AU - Meza-Romero, Roberto
AU - Calkins, Evan
AU - Kent, Gail
AU - Offner, Halina
AU - Bourdette, Dennis
AU - Vandenbark, Arthur A.
N1 - Funding Information:
The contents do not represent the views of the Department of Veterans Affairs or the United States Government. We thank the Advanced Light Microscopy core (grant P30 NS061800) and Histopathology Shared Resource (HSR) for pathology services. The HSR is supported through the OHSU Knight Comprehensive Cancer Institute CCSG: P30 CA069533.
Funding Information:
This work was supported by NIH grants AI 122574 (to AAV) and the Merit Award BX000226 (to AAV) through the Department of Veterans Affairs, Veterans Health Administration, Office of Research and Development, Biomedical Laboratory Research and Development.
Publisher Copyright:
© 2017 The Author(s).
PY - 2017/5/6
Y1 - 2017/5/6
N2 - Background: One of the main challenges in treating multiple sclerosis (MS) is reversing the effects of accumulated damage in the central nervous system (CNS) of progressive MS subjects. While most of the available drugs for MS subjects are anti-inflammatory and thus are limited to relapsing-remitting MS subjects, it is not clear to what extent their effects are capable of inducing axonal repair and remyelination in subjects with chronic MS. Methods: A chronic model of experimental autoimmune encephalomyelitis (EAE) was used to evaluate the potency of partial MHC (pMHC) class II constructs in treating progressive EAE. Results: We demonstrated an estrogen receptor alpha (ERα)-dependent increased dose requirement for effective treatment of female vs. male mice using pMHC. Such treatment using 100-μg doses of RTL342M or DRα1-mMOG-35-55 constructs significantly reversed clinical severity and showed a clear trend for inhibiting ongoing CNS damage, demyelination, and infiltration of inflammatory cells into the CNS in male mice. In contrast, WT female mice required larger 1-mg doses for effective treatment, although lower 100-μg doses were effective in ovariectomized or ERα-deficient mice with EAE. Conclusions: These findings will assist in the design of future clinical trials using pMHC for treatment of progressive MS.
AB - Background: One of the main challenges in treating multiple sclerosis (MS) is reversing the effects of accumulated damage in the central nervous system (CNS) of progressive MS subjects. While most of the available drugs for MS subjects are anti-inflammatory and thus are limited to relapsing-remitting MS subjects, it is not clear to what extent their effects are capable of inducing axonal repair and remyelination in subjects with chronic MS. Methods: A chronic model of experimental autoimmune encephalomyelitis (EAE) was used to evaluate the potency of partial MHC (pMHC) class II constructs in treating progressive EAE. Results: We demonstrated an estrogen receptor alpha (ERα)-dependent increased dose requirement for effective treatment of female vs. male mice using pMHC. Such treatment using 100-μg doses of RTL342M or DRα1-mMOG-35-55 constructs significantly reversed clinical severity and showed a clear trend for inhibiting ongoing CNS damage, demyelination, and infiltration of inflammatory cells into the CNS in male mice. In contrast, WT female mice required larger 1-mg doses for effective treatment, although lower 100-μg doses were effective in ovariectomized or ERα-deficient mice with EAE. Conclusions: These findings will assist in the design of future clinical trials using pMHC for treatment of progressive MS.
KW - Chronic experimental autoimmune encephalomyelitis (EAE)
KW - DRα1-mMOG-35-55
KW - Gender effect
KW - Multiple sclerosis (MS)
KW - RTL342M
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U2 - 10.1186/s12974-017-0873-y
DO - 10.1186/s12974-017-0873-y
M3 - Article
C2 - 28477623
AN - SCOPUS:85018421722
SN - 1742-2094
VL - 14
JO - Journal of Neuroinflammation
JF - Journal of Neuroinflammation
IS - 1
M1 - 100
ER -