نتایج جستجو برای: experimental autoimmune encephalomyelitis

تعداد نتایج: 766438  

2015
Johanna Prinz Aylin Karacivi Eva R. Stormanns Mascha S. Recks Stefanie Kuerten Christoph Kleinschnitz

[This corrects the article DOI: 10.1371/journal.pone.0144847.].

Journal: :The Journal of Experimental Medicine 1999
Kimberly A. Sabelko-Downes Anne H. Cross John H. Russell

We have previously demonstrated a role for Fas and Fas ligand (FasL) in the pathogenesis of experimental allergic encephalomyelitis (EAE). However, using an active induction paradigm we could not distinguish between FasL expressed on activated CD4(+) T cells from that expressed on other inflammatory or resident central nervous system (CNS) cells. To address this issue, we have conducted recipro...

Journal: :The Journal of biological chemistry 2012
Katrien L de Graaf Monika Albert Robert Weissert

It has become increasingly clear that only antibodies recognizing conformation-dependent epitopes of myelin oligodendrocyte glycoprotein (MOG) have a demyelinating potential in the animal model of multiple sclerosis, experimental autoimmune encephalomyelitis (EAE). Nevertheless, for the induction of EAE, most studies to date have used MOG peptides or bacterially expressed MOG, neither of which ...

2012
Taekyun Shin Meejung Ahn Yoh Matsumoto

Experimental autoimmune encephalomyelitis (EAE) in Lewis rats is an acute monophasic paralytic central nervous system disease, in which most rats spontaneously recover from paralysis. EAE in Lewis rats is induced by encephalitogenic antigens, including myelin basic protein. EAE is mediated by CD4(+) Th1 cells, which secrete pro-inflammatory mediators, and spontaneous recovery is mediated by reg...

Journal: :Proceedings of the National Academy of Sciences of the United States of America 2009
Bryan R Becklund Donald W Hansen Hector F Deluca

The active form of vitamin D, 1alpha,25-dihydroxyvitamin D(3) [1,25(OH)(2)D(3)], suppresses disease development in the experimental autoimmune encephalomyelitis (EAE) model of multiple sclerosis (MS). However, complete disease prevention only occurs with doses that dramatically elevate serum calcium levels, thus limiting the usefulness of 1,25(OH)(2)D(3) as a potential MS therapeutic agent. Bec...

2016
Massimo Costanza Rosetta Pedotti

The higher prevalence of multiple sclerosis (MS) in females, along with the modulation of disease activity observed during pregnancy and the post-partum period, has suggested a hormonal influence in MS. Even if prolactin (PRL) does not belong to the sex hormones family, its crucial role in female reproduction and lactation has prompted great efforts to understand if PRL could represent a gender...

2016
Kodai Saitoh Shigeyuki Kon Takuya Nakatsuru Kyosuke Inui Takeru Ihara Naoki Matsumoto Yuichi Kitai Ryuta Muromoto Tadashi Matsuda

Cyclosporin A (CsA) is effective at reducing pathogenic immune responses, but upon withdrawal of CsA the immune response often "rebounds" resulting in a relapse or exacerbation of disease. The mechanisms, cells and cytokines involved in the relapse or exacerbation after CsA withdrawal are unknown. We hypothesized that CsA withdrawal induces IL-17 production that could be responsible for relapse...

Journal: :The Journal of Experimental Medicine 2004
Xue-Feng Bai Ou Li Qunmin Zhou Huiming Zhang Pramod S. Joshi Xincheng Zheng Yan Liu Yin Wang Pan Zheng Yang Liu

In the development of experimental autoimmune encephalomyelitis (EAE), a model for multiple sclerosis (MS), autoreactive T cells must be activated and clonally expand in the lymphoid organs, and then migrate into the central nervous system (CNS) where they undergo further activation. It is unclear whether the autoreactive T cells further expand in the CNS and if so, what interactions are requir...

Journal: :Proceedings of the National Academy of Sciences of the United States of America 2002
Shohei Hori Matthias Haury António Coutinho Jocelyne Demengeot

CD25(+)4(+) regulatory T cells (T(reg)) play an indispensable role in preventing autoimmunity. Little is known, however, about the antigen specificities required for their development and effector functions. Mice transgenic for an anti-myelin basic protein (MBP) T cell antigen receptor (TCR) spontaneously develop experimental autoimmune encephalomyelitis (EAE) when deficient for the RAG-1 gene ...

2015
Heather B. Streeter Rachel Rigden Keith F. Martin Neil J. Scolding David C. Wraith

OBJECTIVE The study was designed to test the efficacy of ATX-MS-1467 in a relevant preclinical model and to assess its safety for the treatment of patients with secondary progressive multiple sclerosis (SPMS). METHODS ATX-MS-1467 was tested for its ability to suppress experimental autoimmune encephalomyelitis (EAE) in the (Ob x DR2)F1 mouse both before and after disease onset. Safety was asse...

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