Low dose zymosan ameliorates both chronic and relapsing Experimental Autoimmune Encephalomyelitis

Autor: Abdolmohamad Rostami, Guang Xian Zhang, Farinaz Safavi, Ghazal Vessal, Hongmei Li, Bardia Nourbakhsh, Patricia Gonnella, Fang Zhou
Jazyk: angličtina
Rok vydání: 2012
Předmět:
CD4-Positive T-Lymphocytes
Lipopolysaccharides
Adoptive cell transfer
Time Factors
Encephalomyelitis
Gene Expression
Severity of Illness Index
T-Lymphocytes
Regulatory

chemistry.chemical_compound
Mice
Secondary Prevention
Immunology and Allergy
Enzyme Inhibitors
Cell Line
Transformed

Experimental autoimmune encephalomyelitis
Anti-Inflammatory Agents
Non-Steroidal

hemic and immune systems
Cell Differentiation
Flow Cytometry
Adoptive Transfer
Neurology
Cytokines
Female
Microglia
Encephalomyelitis
Autoimmune
Experimental

Immunology
Receptors
Antigen
T-Cell

CD11c
Mice
Inbred Strains

Mice
Transgenic

Biology
Tritium
Article
Antigen
Antigens
CD

Nitriles
medicine
Butadienes
Animals
Myelin Proteolipid Protein
MHC class II
Dose-Response Relationship
Drug

Multiple sclerosis
Macrophages
Zymosan
Interferon-alpha
medicine.disease
Coculture Techniques
Peptide Fragments
chemistry
Chronic Disease
biology.protein
Myelin-Oligodendrocyte Glycoprotein
Neurology (clinical)
Popis: 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).
Databáze: OpenAIRE