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Predicate | Object |
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rdf:type | |
lifeskim:mentions | |
pubmed:issue |
5
|
pubmed:dateCreated |
1981-6-13
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pubmed:abstractText |
Cytotoxic T lymphocytes (CTL) against autologous EBV-transformed B lymphoblastoid cell line (LCL) were induced in vitro by culturing peripheral blood lymphocytes (PBL) of healthy donors together with mitomycin C-treated autologous LCL for 6 days. The cytotoxic cells developed only from the E-rosette-positive fraction but not from the negative fraction of PBL. These CTL killed autologous LCL but not PWM-stimulated autologous PBL. In addition, the CTL killed allogeneic LCL when at least 1 of the HLA-A antigens was identical with that of the LCL of CTL donor. However, identity of HLA-B and HLA-C antigens was not enough for a significant killing of allogeneic LCL. The specificity of the CTL was also confirmed by a cold target inhibition test. These results indicated that the CTL induced specifically recognized EBV-transformed cells with HLA restriction.
|
pubmed:language |
eng
|
pubmed:journal | |
pubmed:citationSubset |
AIM
|
pubmed:chemical | |
pubmed:status |
MEDLINE
|
pubmed:month |
May
|
pubmed:issn |
0022-1767
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pubmed:author | |
pubmed:issnType |
Print
|
pubmed:volume |
126
|
pubmed:owner |
NLM
|
pubmed:authorsComplete |
Y
|
pubmed:pagination |
1697-701
|
pubmed:dateRevised |
2006-11-15
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pubmed:meshHeading |
pubmed-meshheading:6163815-Animals,
pubmed-meshheading:6163815-B-Lymphocytes,
pubmed-meshheading:6163815-Callitrichinae,
pubmed-meshheading:6163815-Cell Line,
pubmed-meshheading:6163815-Cell Transformation, Viral,
pubmed-meshheading:6163815-Cytotoxicity, Immunologic,
pubmed-meshheading:6163815-Epitopes,
pubmed-meshheading:6163815-HLA Antigens,
pubmed-meshheading:6163815-Herpesvirus 4, Human,
pubmed-meshheading:6163815-Humans,
pubmed-meshheading:6163815-T-Lymphocytes
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pubmed:year |
1981
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pubmed:articleTitle |
In vitro induction of HLA-restricted cytotoxic T lymphocytes against autologous Epstein-Barr Virus transformed B lymphoblastoid cell line.
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pubmed:publicationType |
Journal Article,
Research Support, Non-U.S. Gov't
|