Switch to
Predicate | Object |
---|---|
rdf:type | |
lifeskim:mentions | |
pubmed:issue |
2
|
pubmed:dateCreated |
1989-2-14
|
pubmed:abstractText |
The present studies were carried out to characterize the influence of the T cell maturation environment on a repertoire of Th cells, T augmenting cells, and Ts cells, which were shown to construct a minimal regulatory circuit to regulate a helper function of class II-restricted Th cells. A repertoire of keyhole limpet hemocyanin-specific Th cells was influenced predominantly by I-A molecules of the T cell maturation environment, whereas a repertoire of T augmenting cells was determined by both I-A and I-E molecules. These repertoires were not influenced by the priming with Ag. A repertoire of Ts cell factor-producing Ts cells was not influenced by the T cell maturation environment, but rather was determined by the I-J haplotype of the APC utilized for priming with Ag. In contrast, a repertoire of novel cognate type Ts cells, which inhibit class II-restricted Th cell function in a restriction-restricted manner, was influenced by both I-A and I-E molecules of the T cell maturation environment. These results demonstrate the two distinct mechanisms for generating a T cell repertoire: a selection by class II molecules of the T cell maturation environment before the priming with foreign Ag and a selection by priming with APC and Ag.
|
pubmed:language |
eng
|
pubmed:journal | |
pubmed:citationSubset |
AIM
|
pubmed:chemical |
http://linkedlifedata.com/resource/pubmed/chemical/Epitopes,
http://linkedlifedata.com/resource/pubmed/chemical/Hemocyanin,
http://linkedlifedata.com/resource/pubmed/chemical/Histocompatibility Antigens Class II,
http://linkedlifedata.com/resource/pubmed/chemical/I-E-antigen,
http://linkedlifedata.com/resource/pubmed/chemical/Suppressor Factors, Immunologic,
http://linkedlifedata.com/resource/pubmed/chemical/keyhole-limpet hemocyanin
|
pubmed:status |
MEDLINE
|
pubmed:month |
Jan
|
pubmed:issn |
0022-1767
|
pubmed:author | |
pubmed:issnType |
Print
|
pubmed:day |
15
|
pubmed:volume |
142
|
pubmed:owner |
NLM
|
pubmed:authorsComplete |
Y
|
pubmed:pagination |
365-73
|
pubmed:dateRevised |
2006-11-15
|
pubmed:meshHeading |
pubmed-meshheading:2463303-Animals,
pubmed-meshheading:2463303-Cell Communication,
pubmed-meshheading:2463303-Cell Differentiation,
pubmed-meshheading:2463303-Epitopes,
pubmed-meshheading:2463303-Hemocyanin,
pubmed-meshheading:2463303-Histocompatibility Antigens Class II,
pubmed-meshheading:2463303-Lymphocyte Activation,
pubmed-meshheading:2463303-Mice,
pubmed-meshheading:2463303-Mice, Inbred BALB C,
pubmed-meshheading:2463303-Mice, Inbred C3H,
pubmed-meshheading:2463303-Mice, Inbred C57BL,
pubmed-meshheading:2463303-Suppressor Factors, Immunologic,
pubmed-meshheading:2463303-T-Lymphocytes, Helper-Inducer,
pubmed-meshheading:2463303-T-Lymphocytes, Regulatory
|
pubmed:year |
1989
|
pubmed:articleTitle |
Generation of T cell repertoire. Two distinct mechanisms for generation of T suppressor cells, T helper cells, and T augmenting cells.
|
pubmed:affiliation |
Department of Immunology, Faculty of Medicine, University of Tokyo, Japan.
|
pubmed:publicationType |
Journal Article,
Research Support, Non-U.S. Gov't
|