rdf:type |
|
lifeskim:mentions |
umls-concept:C0039194,
umls-concept:C0085358,
umls-concept:C0175668,
umls-concept:C0205225,
umls-concept:C0871261,
umls-concept:C1332717,
umls-concept:C1413244,
umls-concept:C1704632,
umls-concept:C1706438,
umls-concept:C1706817,
umls-concept:C2349975,
umls-concept:C2698600,
umls-concept:C2911692
|
pubmed:issue |
10
|
pubmed:dateCreated |
1998-12-15
|
pubmed:abstractText |
Negative as well as positive co-stimulation appears to play an important role in controlling T cell activation. CTLA-4 has been proposed to negatively regulate T cell responses. CTLA-4-deficient mice develop a lymphoproliferative disorder, initiated by the activation and expansion of CD4+ T cells. To assess the function of CTLA-4 on CD8+ T cells, CTLA-4(-/-) animals were crossed to an MHC class I-restricted 2C TCR transgenic mouse line. We demonstrate that although the primary T cell responses were similar, the CTLA-4-deficient 2C TCR+ CD8+ T cells displayed a greater proliferative response upon secondary stimulation than the 2C TCR+ CD8+ T cells from CTLA-4 wild-type mice. These results suggest that CTLA-4 regulates antigen-specific memory CD8+ T cell responses.
|
pubmed:grant |
|
pubmed:language |
eng
|
pubmed:journal |
|
pubmed:citationSubset |
IM
|
pubmed:chemical |
|
pubmed:status |
MEDLINE
|
pubmed:month |
Oct
|
pubmed:issn |
0014-2980
|
pubmed:author |
|
pubmed:issnType |
Print
|
pubmed:volume |
28
|
pubmed:owner |
NLM
|
pubmed:authorsComplete |
Y
|
pubmed:pagination |
3137-43
|
pubmed:dateRevised |
2011-11-17
|
pubmed:meshHeading |
pubmed-meshheading:9808182-Animals,
pubmed-meshheading:9808182-Antigens, CD,
pubmed-meshheading:9808182-Antigens, Differentiation,
pubmed-meshheading:9808182-CD8-Positive T-Lymphocytes,
pubmed-meshheading:9808182-CTLA-4 Antigen,
pubmed-meshheading:9808182-Cell Division,
pubmed-meshheading:9808182-Cells, Cultured,
pubmed-meshheading:9808182-Female,
pubmed-meshheading:9808182-Immunoconjugates,
pubmed-meshheading:9808182-Immunophenotyping,
pubmed-meshheading:9808182-Lymphocyte Activation,
pubmed-meshheading:9808182-Male,
pubmed-meshheading:9808182-Mice,
pubmed-meshheading:9808182-Mice, Inbred C57BL,
pubmed-meshheading:9808182-Mice, Knockout,
pubmed-meshheading:9808182-Mice, Transgenic,
pubmed-meshheading:9808182-Peptides
|
pubmed:year |
1998
|
pubmed:articleTitle |
Secondary but not primary T cell responses are enhanced in CTLA-4-deficient CD8+ T cells.
|
pubmed:affiliation |
Howard Hughes Medical Research Institute, Department of Molecular and Cellular Biology, University of California, Berkeley 94720, USA.
|
pubmed:publicationType |
Journal Article,
Research Support, U.S. Gov't, P.H.S.,
Research Support, Non-U.S. Gov't
|