نتایج جستجو برای: مدل eae

تعداد نتایج: 123229  

حسین بهاروند سعید سمنانیان شیوا خضری, محمد جوان,

زمینه و هدف: افزایش مشارکت سلول های بنیادی عصبی در ترمیم اندوژن آسیب های میلینی یکی از مهم ترین استراتژی ها برای درمان های نوین بیماری ام اس است. افزایش cAMP با فعال کردن PKA و همچنین مستقل از آن، ظرفیت ترمیمی مغز را افزایش می دهد. در مطالعه حاضر، اثر تزریق داخل صفاقی آنالوگ فعال آن (dbcAMP) بر مهاجرت سلول های بنیادی عصبی در مدل EAE بیماری ام اس بررسی شد. مواد و روش ها: در این مطالعه تجربی برای...

2015
Lanfang Zhang Yixian Guo Chang-Qing Xia

In this study, we have evaluated our recently developed method for antigen-cell coupling using sulfosuccinimidyl-4-[N-maleimidomethyl]cyclohexane-1-carboxylate (sulfo-SMCC) heterobifunctional crosslinker in prevention and reversal of experimental autoimmune encephalomyelitis (EAE). We demonstrate that infusion of MOG35-55-coupled spleen cells (MOG-SP) significantly prevents and reverses EAE. Fu...

2012
Youmin Kang Yuhan Sun Jingyao Zhang Wenjuan Gao Jingjing Kang Yongqiang Wang Bin Wang Guoliang Xia

BACKGROUND Regulatory T (Treg) cells can be induced with DNA vaccinations and protect mice from the development of experimental autoimmune encephalomyelitis (EAE), a mouse model of multiple sclerosis (MS). Tacrolimus (FK506) has been shown to have functions on inducing immunosuppression and augmenting apoptosis of pathologic T cells in autoimmune disease. Here we examined the therapeutic effect...

Journal: :Journal of autoimmunity 2000
A Achiron F Mor R Margalit I R Cohen O Lider S Miron

Experimental autoimmune encephalomyelitis (EAE) was induced in Lewis rats either by active immunization with myelin basic protein (MBP) or by adoptive transfer using anti-MBP specific CD4(+)T cells. Treatment with human polyclonal immunoglobulins (IgG) effectively suppressed active EAE. Time-dependent experiments demonstrated that the effect of IgG was manifested only when treatment was given i...

Journal: :European journal of immunology 2009
Magnus Isaksson Brita Ardesjö Lars Rönnblom Olle Kämpe Hans Lassmann Maija-Leena Eloranta Anna Lobell

EAE, an animal model for MS, is a Th17 and Th1-cell-mediated autoimmune disease, but the mechanisms leading to priming of encephalitogenic T cells in autoimmune neuroinflammation are poorly understood. To investigate the role of plasmacytoid DC (pDC) in the initiation of autoimmune Th17- and Th1-cell responses and EAE, we depleted pDC with anti-pDC Ag-1 (anti-PDCA1) mAb prior to immunization of...

Journal: :Proceedings of the National Academy of Sciences of the United States of America 2012
Karola Poppensieker David-Marian Otte Britta Schürmann Andreas Limmer Philipp Dresing Eva Drews Beatrix Schumak Luisa Klotz Jennifer Raasch Alexander Mildner Ari Waisman Stefanie Scheu Percy Knolle Irmgard Förster Marco Prinz Wolfgang Maier Andreas Zimmer Judith Alferink

Dendritic cells (DCs) are pivotal for the development of experimental autoimmune encephalomyelitis (EAE). However, the mechanisms by which they control disease remain to be determined. This study demonstrates that expression of CC chemokine receptor 4 (CCR4) by DCs is required for EAE induction. CCR4(-/-) mice presented enhanced resistance to EAE associated with a reduction in IL-23 and GM-CSF ...

Journal: :Journal of autoimmunity 2004
Enrique Montero Gabriel Nussbaum Joel F Kaye Rolando Perez Agustin Lage Avraham Ben-Nun Irun R Cohen

Experimental Autoimmune Encephalomyelitis (EAE) can be induced in mice of the C57BL/6 strain by subcutaneous immunization with myelin/oligodendrocyte glycoprotein (MOG) peptide p35-55 in CFA, administered twice at an interval of one week and supplemented with Bordetella pertussis toxin given IV. Here, we studied the effect on the induction of EAE of depleting antibodies to CD4, CD8, or CD25 adm...

Journal: :The Journal of neuroscience : the official journal of the Society for Neuroscience 2013
Rory D Spence Amy J Wisdom Yuan Cao Haley M Hill Chandler R L Mongerson Briana Stapornkul Noriko Itoh Michael V Sofroniew Rhonda R Voskuhl

Estrogens can signal through either estrogen receptor α (ERα) or β (ERβ) to ameliorate experimental autoimmune encephalomyelitis (EAE), the most widely used mouse model of multiple sclerosis (MS). Cellular targets of estrogen-mediated neuroprotection are still being elucidated. Previously, we demonstrated that ERα on astrocytes, but not neurons, was critical for ERα ligand-mediated neuroprotect...

Journal: :Journal of Immunology 2023

Abstract Multiple Sclerosis (MS) is a demyelinating autoimmune disease of the central nervous system. Latent infection with Epstein-Barr virus (EBV) has been identified as necessary yet insufficient factor in development disease. Several groups have demonstrated that murine EBV analogue, MHV-68, exacerbates severity experimental encephalomyelitis (EAE). However, induction EAE requires immunizat...

2014
Graham K. Sheridan Kumlesh K. Dev

Fingolimod (FTY720) is an oral therapy for relapsing remitting multiple sclerosis (MS) and targets sphingosine 1-phosphate receptors (S1PRs). FTY720 also rescues animals from experimental autoimmune encephalomyelitis (EAE), an animal model of MS. The protective effects of FTY720 in EAE are primarily scored manually by examining weight loss and limb paralysis that begins around 10-12 days after ...

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