Source:http://linkedlifedata.com/resource/pubmed/id/11785674
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Predicate | Object |
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rdf:type | |
lifeskim:mentions | |
pubmed:issue |
3-4
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pubmed:dateCreated |
2002-1-10
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pubmed:abstractText |
The humoral immune response against alpha(1-->3) dextran (Dex) in BALB/c mice is characterized by the formation of predominantly IgM antibodies bearing the J558 idiotype. IgG antibodies do not appear in euthymic mice. In athymic animals however, the response proceeds to a vigorous IgG production. In euthymic mice formation of IgG is suppressed by J558 idiotype-specific regulatory T cells recognizing in association with I-Ed and in cognate T/B interaction the VH CDR3 derived peptide of the J558 idiotpye. Only B-2 lymphocytes produce IgG whereas B-1 cells do not participate in the production of this Ig class. Using a novel synthetic all alpha(1-->3)-D-gluco configurated tetrasaccharide the Dex-specific B cells can for the first time be analyzed in FACS. In experiments using this newly designed low molecular Dex no signs of B cell apoptosis can be found. This demonstrates a true silencing of persisting Bgamma memory cells and supports previous by adoptive transfer experiments. In this suppression an involvement of CD28/B7-1 interaction can be demonstrated which is a necessary costimulatory suppression signal in addition to the cognate TCR/peptide-I-Ed interaction between J558 Id-specific T cells and J558 idiotype bearing B cells. This results in an activation of 178-4 Ts cells, leading to an overall suppression of the Dex-specific IgG isotype production on the one hand and on the other hand provides a signal for the survival and clonal expansion of J558 Id-positive B cells.
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pubmed:language |
eng
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pubmed:journal | |
pubmed:citationSubset |
IM
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pubmed:chemical |
http://linkedlifedata.com/resource/pubmed/chemical/Antibodies, Bacterial,
http://linkedlifedata.com/resource/pubmed/chemical/Antigens, CD28,
http://linkedlifedata.com/resource/pubmed/chemical/Antigens, CD80,
http://linkedlifedata.com/resource/pubmed/chemical/Complementarity Determining Regions,
http://linkedlifedata.com/resource/pubmed/chemical/Dextrans,
http://linkedlifedata.com/resource/pubmed/chemical/Polysaccharides, Bacterial,
http://linkedlifedata.com/resource/pubmed/chemical/alpha-1,3-dextran
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pubmed:status |
MEDLINE
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pubmed:issn |
1044-6672
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pubmed:author | |
pubmed:issnType |
Print
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pubmed:volume |
8
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pubmed:owner |
NLM
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pubmed:authorsComplete |
Y
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pubmed:pagination |
243-57
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pubmed:dateRevised |
2008-11-20
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pubmed:meshHeading |
pubmed-meshheading:11785674-Animals,
pubmed-meshheading:11785674-Antibodies, Bacterial,
pubmed-meshheading:11785674-Antigens, CD28,
pubmed-meshheading:11785674-Antigens, CD80,
pubmed-meshheading:11785674-Apoptosis,
pubmed-meshheading:11785674-Cell Culture Techniques,
pubmed-meshheading:11785674-Complementarity Determining Regions,
pubmed-meshheading:11785674-Dextrans,
pubmed-meshheading:11785674-Lymphocyte Cooperation,
pubmed-meshheading:11785674-Mice,
pubmed-meshheading:11785674-Mice, Inbred BALB C,
pubmed-meshheading:11785674-Models, Immunological,
pubmed-meshheading:11785674-Plasma Cells,
pubmed-meshheading:11785674-Polysaccharides, Bacterial,
pubmed-meshheading:11785674-T-Lymphocytes
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pubmed:year |
2001
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pubmed:articleTitle |
T cell mediated antibody invariance in an immune response against a bacterial carbohydrate antigen requires CD28/B7-1 costimulation.
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pubmed:affiliation |
Institute for Immunology, University of Münster, Germany. rademae@uni-muenster.de
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pubmed:publicationType |
Journal Article,
Research Support, Non-U.S. Gov't
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