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rdf:type | |
lifeskim:mentions | |
pubmed:dateCreated |
1988-8-19
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pubmed:abstractText |
The objective of the studies reported herein was to identify and characterize T cell and B cell recognition sites within the pre-S regions of HBsAg/p39, and to analyze functional T-cell-B cell interactions at the level of in vivo antibody production. The results indicate: (1) several peptides within the pre-S(1) region of HBsAg were identified which can induce and elicit HBsAg/p39-specific T-cell proliferation; (2) a 10 amino acid peptide, p12-21, and the 94-117 sequence define pre-S(1)-specific T-cell recognition sites; (3) five distinct, pre-S(1)-specific antibody binding sites and 2 pre-S(2)-specific antibody binding sites were identified; (4) synthetic pre-S(1) region T-cell determinants can prime in vivo antibody production to multiple B-cell epitopes within the pre-S(2) and S regions, as well as within the pre-S(1) region; and (5) specificity of the primed T cell population can influence the specificity of the B-cell response.
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pubmed:grant | |
pubmed:language |
eng
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pubmed:journal | |
pubmed:citationSubset |
IM
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pubmed:chemical | |
pubmed:status |
MEDLINE
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pubmed:issn |
0065-2598
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pubmed:author | |
pubmed:issnType |
Print
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pubmed:volume |
225
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pubmed:owner |
NLM
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pubmed:authorsComplete |
Y
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pubmed:pagination |
233-9
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pubmed:dateRevised |
2011-11-17
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pubmed:meshHeading |
pubmed-meshheading:2455965-Animals,
pubmed-meshheading:2455965-Binding Sites, Antibody,
pubmed-meshheading:2455965-Epitopes,
pubmed-meshheading:2455965-H-2 Antigens,
pubmed-meshheading:2455965-Hepatitis B Surface Antigens,
pubmed-meshheading:2455965-Lymphocyte Activation,
pubmed-meshheading:2455965-Mice,
pubmed-meshheading:2455965-Phenotype,
pubmed-meshheading:2455965-T-Lymphocytes
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pubmed:year |
1987
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pubmed:articleTitle |
T-cell recognition of pre-S regions of HBsAg can bypass nonresponse to the S region.
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pubmed:affiliation |
Department of Basic and Clinical Research, Scripps Clinic and Research Foundation, La Jolla, CA.
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pubmed:publicationType |
Journal Article,
Research Support, U.S. Gov't, P.H.S.,
Research Support, Non-U.S. Gov't
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