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Sex-dependent treatment of chronic EAE with partial MHC class II constructs

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-remittin...

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Autores principales: Benedek, Gil, Chaudhary, Priya, Meza-Romero, Roberto, Calkins, Evan, Kent, Gail, Offner, Halina, Bourdette, Dennis, Vandenbark, Arthur A.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: BioMed Central 2017
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5420407/
https://www.ncbi.nlm.nih.gov/pubmed/28477623
http://dx.doi.org/10.1186/s12974-017-0873-y
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author Benedek, Gil
Chaudhary, Priya
Meza-Romero, Roberto
Calkins, Evan
Kent, Gail
Offner, Halina
Bourdette, Dennis
Vandenbark, Arthur A.
author_facet Benedek, Gil
Chaudhary, Priya
Meza-Romero, Roberto
Calkins, Evan
Kent, Gail
Offner, Halina
Bourdette, Dennis
Vandenbark, Arthur A.
author_sort Benedek, Gil
collection PubMed
description 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. ELECTRONIC SUPPLEMENTARY MATERIAL: The online version of this article (doi:10.1186/s12974-017-0873-y) contains supplementary material, which is available to authorized users.
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spelling pubmed-54204072017-05-08 Sex-dependent treatment of chronic EAE with partial MHC class II constructs Benedek, Gil Chaudhary, Priya Meza-Romero, Roberto Calkins, Evan Kent, Gail Offner, Halina Bourdette, Dennis Vandenbark, Arthur A. J Neuroinflammation Research 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. ELECTRONIC SUPPLEMENTARY MATERIAL: The online version of this article (doi:10.1186/s12974-017-0873-y) contains supplementary material, which is available to authorized users. BioMed Central 2017-05-06 /pmc/articles/PMC5420407/ /pubmed/28477623 http://dx.doi.org/10.1186/s12974-017-0873-y Text en © The Author(s). 2017 Open AccessThe article is a work of the United States Government; Title 17 U.S.C 105 provides that copyright protection is not available for any work of the United States government in the United States. Additionally, this is an open access article distributed under the terms of the Creative Commons Public Domain Dedication waiver (http://creativecommons.org/publicdomain/zero/1.0/ ), which permits worldwide unrestricted use, distribution, and reproduction in any medium for any lawful purpose.
spellingShingle Research
Benedek, Gil
Chaudhary, Priya
Meza-Romero, Roberto
Calkins, Evan
Kent, Gail
Offner, Halina
Bourdette, Dennis
Vandenbark, Arthur A.
Sex-dependent treatment of chronic EAE with partial MHC class II constructs
title Sex-dependent treatment of chronic EAE with partial MHC class II constructs
title_full Sex-dependent treatment of chronic EAE with partial MHC class II constructs
title_fullStr Sex-dependent treatment of chronic EAE with partial MHC class II constructs
title_full_unstemmed Sex-dependent treatment of chronic EAE with partial MHC class II constructs
title_short Sex-dependent treatment of chronic EAE with partial MHC class II constructs
title_sort sex-dependent treatment of chronic eae with partial mhc class ii constructs
topic Research
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5420407/
https://www.ncbi.nlm.nih.gov/pubmed/28477623
http://dx.doi.org/10.1186/s12974-017-0873-y
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