Literature DB >> 23010280

Low dose zymosan ameliorates both chronic and relapsing experimental autoimmune encephalomyelitis.

Hongmei Li1, Patricia Gonnella, Farinaz Safavi, Ghazal Vessal, Bardia Nourbakhsh, Fang Zhou, Guang-Xian Zhang, Abdolmohamad Rostami.   

Abstract

Zymosan has previously been reported to have both pro-inflammatory and anti-inflammatory effects. Here we demonstrate that low dose zymosan prevented or reversed chronic and relapsing paralysis in EAE. In suppressing CNS autoimmune inflammation, zymosan not only regulated APC costimulator and MHC class II expression, but also promoted differentiation of regulatory T cells. Following adoptive transfer of zymosan-primed CD4(+) T cells, recipient mice were protected from EAE. In contrast, a MAPK inhibitor and a blocker of β-glucan, reversed the effects of zymosan. These results demonstrate that zymosan may be a promising beneficial agent for Multiple Sclerosis (MS).
Copyright © 2012 Elsevier B.V. All rights reserved.

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Year:  2012        PMID: 23010280      PMCID: PMC3534935          DOI: 10.1016/j.jneuroim.2012.08.013

Source DB:  PubMed          Journal:  J Neuroimmunol        ISSN: 0165-5728            Impact factor:   3.478


  54 in total

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5.  The influence of interferon-gamma and various phagocytic stimuli on the expression of MHC-class II antigens on human monocytes--relation to the generation of reactive oxygen intermediates.

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3.  Fungal β-glucan, a Dectin-1 ligand, promotes protection from type 1 diabetes by inducing regulatory innate immune response.

Authors:  Subha Karumuthil-Melethil; Radhika Gudi; Benjamin M Johnson; Nicolas Perez; Chenthamarakshan Vasu
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7.  Protective effects of zymosan on heat stress-induced immunosuppression and apoptosis in dairy cows and peripheral blood mononuclear cells.

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8.  T cell activation status determines the cytokine pattern induced by zymosan and bacterial DNA both in thymocytes and splenocytes.

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10.  Stimulation of macrophages with the β-glucan produced by aureobasidium pullulans promotes the secretion of tumor necrosis factor-related apoptosis inducing ligand (TRAIL).

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