NFAT-controlled expression of GFP permits visualization and isolation of antigen-stimulated primary human T cells

We have developed a new method that allows detection and isolation of viabl e, antigen-specific, human T cells from a heterogeneous pool of T cells. We have engineered a self-inactivating retroviral vector containing multiple (3 or 6) nuclear factor of activated T-cell (NFAT)-binding sites, followed by the minimal IL2 promoter and the reporter gene GFP, Jurkat cells, primar y T-cell blasts, and T-cell clones were transduced with high efficiency (20 %-40%), Stimulation of the transduced cells with phorbol myristate acetate (PMA) and ionomycin resulted in a high level expression of GFP that was max imal after 12 to 14 hours and remained stable for another 12 hours. Activat ion of T cells carrying the construct containing 6 NFAT-binding sites resul ted in the highest mean fluorescence intensity. Cyclosporin-A and FK506 wer e able to block the activation-dependent GFP expression. Activation of tran sduced T-cell blasts with the superantigen staphylococcal enterotoxin B or of transduced antigen-specific T-cell clones with cognate antigen resulted in GFP expression. After an overnight stimulation of a heterogeneous T-cell bulk culture with an HLA mismatched stimulator cell (JY), the GFP expressi ng cells were cloned. As expected, the cloning frequency of the antigen-spe cific GFP(+) cells was considerably higher than that of the total T-cell po pulation. Most of the T-cell clones were either cytolytic, or proliferative toward JY stimulator cells. Interestingly, we also isolated T-cell clones that were noncytolytic and nonproliferative toward Jy cells, but specifical ly up-regulated GFP after an overnight stimulation with JY. (C) 2000 by The American Society of Hematology.