Statements in which the resource exists as a subject.
PredicateObject
rdf:type
lifeskim:mentions
pubmed:issue
5
pubmed:dateCreated
2009-5-14
pubmed:abstractText
Adoptive T-cell transfer of in vitro cultured T cells derived from cancer patients with naturally developed immune responses has met with some success as an immunotherapeutic approach, although only a limited number of patients showed spontaneous immune responses. To find alternative ways, such as cancer-specific T-cell receptor (TCR) gene transfer, in preparation for sufficient numbers of antigen-specific T cells is an important issue in the field of adoptive T-cell therapy. Given the inherent disadvantage of alphabeta TCR transfer to other alphabeta T cells, namely the possible formation of mixed TCR heterodimers with endogenous alpha or beta TCR, we employed gammadelta T cells as a target for retroviral transfer of cancer-specific TCR and examined whether gammadelta T cells were useful as an alternative population for TCR transfer. Although retroviral transduction to gammadelta T cells with TCR alphabeta genes alone, isolated from a MAGE-A4(143-151)-specific alphabeta CD8(+) cytotoxic T lymphocyte (CTL) clone, did not provide sufficient affinity to recognize major histocompatibility (MHC)-peptide complexes due to the lack of CD8 co-receptor, gammadelta T cells co-transduced with TCR alphabeta and CD8 alphabeta genes acquired cytotoxicity against tumor cells and produced cytokines in both alphabeta- and gammadelta-TCR-dependent manners. Furthermore, alphabeta TCR and CD8-transduced gammadelta T cells, stimulated either through alphabeta TCR or gammadelta TCR, rapidly responded to target cells compared with conventional alphabeta T cells, reminiscent of gammadelta T cells. We propose alphabeta TCR-transduced gammadelta T cells as an alternative strategy for adoptive T-cell transfer.
pubmed:language
eng
pubmed:journal
pubmed:citationSubset
IM
pubmed:chemical
pubmed:status
MEDLINE
pubmed:month
May
pubmed:issn
1476-5462
pubmed:author
pubmed:issnType
Electronic
pubmed:volume
16
pubmed:owner
NLM
pubmed:authorsComplete
Y
pubmed:pagination
620-8
pubmed:meshHeading
pubmed-meshheading:19242528-Adoptive Transfer, pubmed-meshheading:19242528-CD8-Positive T-Lymphocytes, pubmed-meshheading:19242528-Cytotoxicity, Immunologic, pubmed-meshheading:19242528-Enzyme-Linked Immunosorbent Assay, pubmed-meshheading:19242528-Gene Therapy, pubmed-meshheading:19242528-Genes, Neoplasm, pubmed-meshheading:19242528-Genetic Vectors, pubmed-meshheading:19242528-Humans, pubmed-meshheading:19242528-Lymphocyte Activation, pubmed-meshheading:19242528-Lymphocyte Transfusion, pubmed-meshheading:19242528-Neoplasms, pubmed-meshheading:19242528-Receptors, Antigen, T-Cell, alpha-beta, pubmed-meshheading:19242528-Receptors, Antigen, T-Cell, gamma-delta, pubmed-meshheading:19242528-Retroviridae, pubmed-meshheading:19242528-T-Cell Antigen Receptor Specificity, pubmed-meshheading:19242528-Transduction, Genetic, pubmed-meshheading:19242528-Tumor Cells, Cultured
pubmed:year
2009
pubmed:articleTitle
Rapid alphabeta TCR-mediated responses in gammadelta T cells transduced with cancer-specific TCR genes.
pubmed:affiliation
Department of Immunno-Gene Therapy, Mie University Graduate School of Medicine, Mie, Japan.
pubmed:publicationType
Journal Article, Research Support, Non-U.S. Gov't