6533b856fe1ef96bd12b27b5
RESEARCH PRODUCT
Facilitating matched pairing and expression of TCR chains introduced into human T cells.
Ralf-holger VossCarla FowlerCarla FowlerMatthias WolflMatthias WolflMichelle L. DossettMichelle L. DossettWilliam Y. HoWilliam Y. HoPhilip D. GreenbergPhilip D. GreenbergJürgen KuballJürgen Kuballsubject
GeneticsAdoptive cell transferTranscription GeneticCD3T-LymphocytesImmunologyGenetic transferT-cell receptorReceptors Antigen T-CellCell BiologyHematologyT lymphocyteGene TherapyBiologyBiochemistryCell biologyCell LineAntigenCell cultureProtein Biosynthesisbiology.proteinHumansCysteineReceptordescription
AbstractAdoptive transfer of T lymphocytes is a promising treatment for a variety of malignancies but often not feasible due to difficulties generating T cells that are reactive with the targeted antigen from patients. To facilitate rapid generation of cells for therapy, T cells can be programmed with genes encoding the α and β chains of an antigen-specific T-cell receptor (TCR). However, such exogenous α and β chains can potentially assemble as pairs not only with each other but also with endogenous TCR α and β chains, thereby generating αβTCR pairs of unknown specificity as well as reducing the number of exogenous matched αβTCR pairs at the cell surface. We demonstrate that introducing cysteines into the constant region of the α and β chains can promote preferential pairing with each other, increase total surface expression of the introduced TCR chains, and reduce mismatching with endogenous TCR chains. This approach should improve both the efficacy and safety of ongoing efforts to use TCR transfer as a strategy to generate tumor-reactive T cells.
year | journal | country | edition | language |
---|---|---|---|---|
2006-11-04 | Blood |