Statements in which the resource exists as a subject.
PredicateObject
rdf:type
lifeskim:mentions
pubmed:issue
4
pubmed:dateCreated
2010-1-15
pubmed:abstractText
There is evidence that in the acute axonal motor neuropathy (AMAN) subtype of Guillain-Barré syndrome antibodies to gangliosides, produced through molecular mimicry by antecedent Campylobacter jejuni (C. jejuni) infection, attack gangliosides expressed in human peripheral nerve axolemma, inducing a primary axonal damage. The aim of this study is to investigate whether the T cell response has a role in AMAN pathogenesis. We isolated monocytes from 4 healthy subjects and 5 AMAN patients with antecedent C. jejuni infection and antibodies to GM1 and/or GD1a gangliosides. Immature dendritic cells expressing CD1 molecules cultured with autologous T cells were stimulated with 2 lipopolysaccharides (LPSs) extracted from C. jejuni strains containing GM1 and GD1a-like structures and with GM1 and GD1a. The T cell response to LPSs and to gangliosides was determined by measuring the release of IFN-gamma and TNF-alpha. We observed a T cell response to both LPSs in controls and AMAN patients, whereas only AMAN patients showed T cell reactivity to gangliosides GM1 and GD1a with a tight correlation between T cell reactivity to the ganglioside and individual antibody responses to the same ganglioside. T cells responding to gangliosides were CD1c-restricted CD8 positive and CD27 negative. These findings indicate a contribution of cellular immunity in the pathogenesis of AMAN. A possible role for ganglioside-reactive T cells might be to facilitate the production of antibodies against gangliosides.
pubmed:language
eng
pubmed:journal
pubmed:citationSubset
IM
pubmed:chemical
pubmed:status
MEDLINE
pubmed:issn
0394-6320
pubmed:author
pubmed:issnType
Print
pubmed:volume
22
pubmed:owner
NLM
pubmed:authorsComplete
Y
pubmed:pagination
1043-50
pubmed:meshHeading
pubmed-meshheading:20074468-Acute Disease, pubmed-meshheading:20074468-Adult, pubmed-meshheading:20074468-Aged, pubmed-meshheading:20074468-Antibodies, pubmed-meshheading:20074468-Antigens, CD1, pubmed-meshheading:20074468-Antigens, CD27, pubmed-meshheading:20074468-Axons, pubmed-meshheading:20074468-CD8-Positive T-Lymphocytes, pubmed-meshheading:20074468-Campylobacter Infections, pubmed-meshheading:20074468-Campylobacter jejuni, pubmed-meshheading:20074468-Case-Control Studies, pubmed-meshheading:20074468-Cells, Cultured, pubmed-meshheading:20074468-Coculture Techniques, pubmed-meshheading:20074468-Cytotoxicity, Immunologic, pubmed-meshheading:20074468-Dendritic Cells, pubmed-meshheading:20074468-Female, pubmed-meshheading:20074468-G(M1) Ganglioside, pubmed-meshheading:20074468-Gangliosides, pubmed-meshheading:20074468-Glycoproteins, pubmed-meshheading:20074468-Guillain-Barre Syndrome, pubmed-meshheading:20074468-Humans, pubmed-meshheading:20074468-Immunity, Cellular, pubmed-meshheading:20074468-Immunophenotyping, pubmed-meshheading:20074468-Interferon-gamma, pubmed-meshheading:20074468-Lipopolysaccharides, pubmed-meshheading:20074468-Male, pubmed-meshheading:20074468-Middle Aged, pubmed-meshheading:20074468-Motor Neuron Disease, pubmed-meshheading:20074468-Motor Neurons, pubmed-meshheading:20074468-Tumor Necrosis Factor-alpha, pubmed-meshheading:20074468-Young Adult
pubmed:articleTitle
T cell response in acute motor axonal neuropathy.
pubmed:affiliation
Neuroimmunology Unit, European Centre for Brain Research, Santa Lucia Foundation, Rome, Italy.
pubmed:publicationType
Journal Article, Research Support, Non-U.S. Gov't