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Predicate | Object |
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rdf:type | |
lifeskim:mentions | |
pubmed:issue |
2
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pubmed:dateCreated |
1996-11-7
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pubmed:abstractText |
To enable construction of CTL with known predefined Ab specificity for adoptive immunotherapy, we constructed a chimeric scFv/gamma gene composed of the variable regions of a mAb joined to the Fc(epsilon)RI signaling receptor gamma-chain of mast cells. Introduction of this chimeric receptor into CTL rendered these lymphocytes specific for renal cell carcinoma. This approach combines the specificity of tumor-selective Abs with the efficacy of CTL to destroy tumor cells. We not only demonstrated that the transduced CTL functionally express the scFv/gamma receptor for a prolonged period of time (4.5 mo of in vitro culture), but also showed high levels of Ab-dictated lysis of renal cell carcinoma similar to that of normal CTL, and importantly, we demonstrated that these CTL can recycle their lytic activity. Moreover, these scFv/gamma-expressing T lymphocytes produce cytokines upon stimulation with the relevant target cell. These results together with the donor independence of our gene transduction protocol demonstrate the feasibility of redirecting T lymphocytes for cancer treatment.
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pubmed:language |
eng
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pubmed:journal | |
pubmed:citationSubset |
AIM
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pubmed:chemical |
http://linkedlifedata.com/resource/pubmed/chemical/Cytokines,
http://linkedlifedata.com/resource/pubmed/chemical/Immunoglobulin Fragments,
http://linkedlifedata.com/resource/pubmed/chemical/Immunoglobulin G,
http://linkedlifedata.com/resource/pubmed/chemical/Receptors, IgE,
http://linkedlifedata.com/resource/pubmed/chemical/Recombinant Fusion Proteins,
http://linkedlifedata.com/resource/pubmed/chemical/immunoglobulin Fv
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pubmed:status |
MEDLINE
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pubmed:month |
Jul
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pubmed:issn |
0022-1767
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pubmed:author | |
pubmed:issnType |
Print
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pubmed:day |
15
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pubmed:volume |
157
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pubmed:owner |
NLM
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pubmed:authorsComplete |
Y
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pubmed:pagination |
836-43
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pubmed:dateRevised |
2006-11-15
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pubmed:meshHeading |
pubmed-meshheading:8752936-Base Sequence,
pubmed-meshheading:8752936-Carcinoma, Renal Cell,
pubmed-meshheading:8752936-Cytokines,
pubmed-meshheading:8752936-Cytotoxicity, Immunologic,
pubmed-meshheading:8752936-Cytotoxicity Tests, Immunologic,
pubmed-meshheading:8752936-Genes, Immunoglobulin,
pubmed-meshheading:8752936-Genetic Vectors,
pubmed-meshheading:8752936-Humans,
pubmed-meshheading:8752936-Immunoglobulin Fragments,
pubmed-meshheading:8752936-Immunoglobulin G,
pubmed-meshheading:8752936-Molecular Sequence Data,
pubmed-meshheading:8752936-Receptors, IgE,
pubmed-meshheading:8752936-Recombinant Fusion Proteins,
pubmed-meshheading:8752936-T-Lymphocytes, Cytotoxic,
pubmed-meshheading:8752936-Transfection,
pubmed-meshheading:8752936-Tumor Cells, Cultured
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pubmed:year |
1996
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pubmed:articleTitle |
Single chain Ig/gamma gene-redirected human T lymphocytes produce cytokines, specifically lyse tumor cells, and recycle lytic capacity.
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pubmed:affiliation |
Department of Clinical and Tumor Immunology, Daniel den Hoed Cancer Center, Rotterdam, The Netherlands.
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pubmed:publicationType |
Journal Article,
Research Support, Non-U.S. Gov't
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