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Predicate | Object |
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rdf:type | |
lifeskim:mentions | |
pubmed:issue |
6
|
pubmed:dateCreated |
1977-1-29
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pubmed:abstractText |
Immunization with increasing doses of SRBC, in excess of 10(8), results in a progressive decline in the anti-SRBC PFC response. This hyporesponsive state is antigen specific and is reflected in a decrease of both T helper and B antibody-forming activity. We asked whether the apparent defect of T helper activity reflected a) an absence of alphaSRBC helper T cell activity, or b) the presence of SRBC-specific suppressor T cells within the hyporesponsive population. Our results indicate that at least a portion of hyporesponsiveness noted after antigen exposure to large doses of antigen can be ascribed to specific suppressor T cell activation. Fractionation of the suppressive T cell population using Ly antiserum showed that specific suppressive activity was mediated by a subclass of T cells (Ly2+), distinct from that committed to express helper function (Ly1).
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pubmed:language |
eng
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pubmed:journal | |
pubmed:citationSubset |
AIM
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pubmed:chemical | |
pubmed:status |
MEDLINE
|
pubmed:month |
Dec
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pubmed:issn |
0022-1767
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pubmed:author | |
pubmed:issnType |
Print
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pubmed:volume |
117
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pubmed:owner |
NLM
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pubmed:authorsComplete |
Y
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pubmed:pagination |
2209-12
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pubmed:dateRevised |
2006-11-15
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pubmed:meshHeading |
pubmed-meshheading:62809-Animals,
pubmed-meshheading:62809-Antigen-Antibody Reactions,
pubmed-meshheading:62809-Cell Separation,
pubmed-meshheading:62809-Dose-Response Relationship, Immunologic,
pubmed-meshheading:62809-Epitopes,
pubmed-meshheading:62809-Hemolytic Plaque Technique,
pubmed-meshheading:62809-Immunity, Cellular,
pubmed-meshheading:62809-Immunosuppression,
pubmed-meshheading:62809-Mice,
pubmed-meshheading:62809-Mice, Inbred C57BL,
pubmed-meshheading:62809-Sheep,
pubmed-meshheading:62809-Spleen,
pubmed-meshheading:62809-T-Lymphocytes
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pubmed:year |
1976
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pubmed:articleTitle |
Maintenance of hyporesponsiveness to antigen by a distinct subclass of T lymphocytes.
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pubmed:publicationType |
Journal Article,
Research Support, U.S. Gov't, P.H.S.
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