In this multi-center open-label, non-randomized phase I/II intervention study three consecutive doses of donor-derived EBV Tscm-CTLs will be administered to 10 patients with treatment-refractory EBV lymphoma, diseases or PTLDs. EBV Tscm-CTLs will derive from hematopoietic cell transplant (HCT) or third-party donors.
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Assessment of feasibility to expand Tscm-enriched EBV CTLs
Timeframe: one time assessment on day 9-11 of expansion before cryopreservation (plus at least 7 days for microbiological culture)
Safety of EBV Tscm-CTL infusion assessed by number of early infusion-related events
Timeframe: up to 12 hours after first dose of EBV Tscm-CTL infusion
Safety of EBV Tscm-CTL infusion assessed by number of late clinical reaction to EBV Tscm-CTLs
Timeframe: from 12 hours after first dose until 3 months after the last dose of EBV CTLs