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Predicate | Object |
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rdf:type | |
lifeskim:mentions | |
pubmed:issue |
6089
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pubmed:dateCreated |
1986-11-25
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pubmed:abstractText |
We have recently derived a series of cloned cell lines displaying natural killer (NK) cell-like activity from normal human fetal blood (25 weeks). The lines were obtained after repeated stimulation of mononuclear cells with allogeneic Epstein-Barr virus (EBV)-transformed B lymphocytes and are interleukin-2 (IL-2) dependent. Initial characterization of the clones has been reported previously. Certain of these clones have been found to have unusual surface characteristics, namely, they are recognized by several well-defined anti-T3 antibodies, but do not react with WT31, which is thought to recognise an invariant epitope of the human (Ti-alpha beta) structure. Transcription of the genes encoding the alpha- and beta-chains of the T-cell receptor was assessed in two of these clones (F6A4 and F6C7). Ti-beta genes were found to be expressed, whereas alpha messenger RNA was not detected in Northern blot analysis. These data strongly suggest that these cells do not produce a stoichiometric T3/Ti-alpha beta receptor complex. However, experiments performed with a monoclonal antibody (anti-NKFi) developed against F6C7 cells demonstrated the existence of a unique clonotypic structure [relative molecular mass (Mr) 85,000 (85K)] which is surface-associated with T3 proteins. Furthermore, both anti-T3 and anti-NKFi were found to block cytotoxic effector function. Together, the results support the view that T3 proteins are involved in non-major histocompatibility complex (MHC)-restricted cytotoxic reactions mediated by certain circulating fetal lymphocytes which are likely to use a clonotypic structure distinct from both the 'first' (alpha beta) and the putative 'second' (gamma delta) T-cell receptor to recognize their target. The present studies were designed to characterize this structure.
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pubmed:language |
eng
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pubmed:journal | |
pubmed:citationSubset |
IM
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pubmed:chemical |
http://linkedlifedata.com/resource/pubmed/chemical/Antibodies, Monoclonal,
http://linkedlifedata.com/resource/pubmed/chemical/Antigens, Differentiation...,
http://linkedlifedata.com/resource/pubmed/chemical/Antigens, Surface,
http://linkedlifedata.com/resource/pubmed/chemical/Macromolecular Substances,
http://linkedlifedata.com/resource/pubmed/chemical/RNA, Messenger,
http://linkedlifedata.com/resource/pubmed/chemical/Receptors, Antigen, T-Cell
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pubmed:status |
MEDLINE
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pubmed:issn |
0028-0836
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pubmed:author | |
pubmed:issnType |
Print
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pubmed:volume |
323
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pubmed:owner |
NLM
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pubmed:authorsComplete |
N
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pubmed:pagination |
638-40
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pubmed:dateRevised |
2006-11-15
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pubmed:meshHeading |
pubmed-meshheading:3095661-Antibodies, Monoclonal,
pubmed-meshheading:3095661-Antigens, Differentiation, T-Lymphocyte,
pubmed-meshheading:3095661-Antigens, Surface,
pubmed-meshheading:3095661-Cell Differentiation,
pubmed-meshheading:3095661-Cell Line,
pubmed-meshheading:3095661-Cytotoxicity, Immunologic,
pubmed-meshheading:3095661-Fetal Blood,
pubmed-meshheading:3095661-Gene Expression Regulation,
pubmed-meshheading:3095661-Humans,
pubmed-meshheading:3095661-Immunity, Cellular,
pubmed-meshheading:3095661-Immunologic Capping,
pubmed-meshheading:3095661-Killer Cells, Natural,
pubmed-meshheading:3095661-Lymphocytes,
pubmed-meshheading:3095661-Macromolecular Substances,
pubmed-meshheading:3095661-RNA, Messenger,
pubmed-meshheading:3095661-Receptors, Antigen, T-Cell
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pubmed:articleTitle |
A unique T-cell receptor complex expressed on human fetal lymphocytes displaying natural-killer-like activity.
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pubmed:publicationType |
Journal Article,
Research Support, Non-U.S. Gov't
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