Treatment of CMV in a patient with profound combined immunodeficiency, who has viremia and pneumonia, using CMV-specific donor-derived T lymphocytes (CMV-VST).
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Feasibility of study
Timeframe: Enrollment to 24 months
Incidence of Treatment-Emergent Adverse Events [Safety and Tolerability]
Timeframe: Weekly to 3 months
Efficacy of Intervention
Timeframe: Weekly to 3 months
Efficacy of Intervention
Timeframe: Monthly from 3 to 12 months
Efficacy of Intervention
Timeframe: Every 3 months from 12-24 months