A polysaccharide from the human commensal Bacteroides fragilis protects against CNS demyelinating disease
Author(s) -
Javier OchoaRepáraz,
Daniel W. Mielcarz,
Y Wang,
Sakhina Begum-Haque,
Suryasarathi Dasgupta,
Dennis L. Kasper,
L H Kasper
Publication year - 2010
Publication title -
mucosal immunology
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 3.596
H-Index - 101
eISSN - 1935-3456
pISSN - 1933-0219
DOI - 10.1038/mi.2010.29
Subject(s) - bacteroides fragilis , multiple sclerosis , immunology , immune system , experimental autoimmune encephalomyelitis , foxp3 , microbiology and biotechnology , demyelinating disease , biology , encephalomyelitis , medicine , antibiotics
The intestinal microbiome may have a critical roll in susceptibility or resistance to immune-mediated diseases. Alterations of the gut microflora after oral antibiotic treatment can regulate encephalomyelitis (EAE), an animal model for human multiple sclerosis (MS). We now show that a zwitterionic capsular polysaccharide A (PSA) of Bacteroides fragilis can protect against central nervous system demyelinating disease. Oral administration with purified PSA protected mice against EAE prophylactic and therapeutically. PSA treatment enhanced CD103 expressing dendritic cells (DCs) that accumulated in the cervical lymph nodes. Exposure of naïve DCs to PSA induced the conversion of naïve CD4(+) T cells into interleukin (IL)-10-producing FoxP3(+)Treg cells. Protection against EAE was completely abrogated in IL-10-deficient mice. Our results show an important role for a molecule from human commensal bacteria in protecting against EAE and suggest the possibility for protection in MS.
Accelerating Research
Robert Robinson Avenue,
Oxford Science Park, Oxford
OX4 4GP, United Kingdom
Address
John Eccles HouseRobert Robinson Avenue,
Oxford Science Park, Oxford
OX4 4GP, United Kingdom