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</script>Flow cytometry and TCR sequencing dataset from the ACES study (NCT03475212), a phase II multicenter consortium study for the treatment of pediatric patients with inborn errors of immunity and/or post allogeneic hematopoietic stem cell transplant with refractory viral infections using partially-HLA matched virus-specific T cells targeting cytomegalovirus, Epstein-Barr virus, or adenovirus. Recipients of virus-specific T cell infusions were evaluated at multiple time points before and after infusion, with a focus on days 0, 14, 28, 45, and 90. Recipient T cells were expanded in vitra against the targeted viruses for 10 days and then re-stimulated with viral peptide libraries (CMV pp65/IE1, EBV EBNA1/LMP2, Adenovirus hexon/penton) and evaluated by intracellular cytokine staining. Staining of disparate HLA alleles between the VST donor and HSCT donor was included where possible. T cell receptor beta chain sequencing was performed on availble virus-specific T cell (VST) products and recipient blood samples (bulk PBMCs or sorted T cells) in order to track virus-specific clonotypes. Where possible, VSTs were stimulated with viral peptide libraries and sorted to isolate Interferon-gamma+ T cells for TCR sequencing of antigen-specific T cells. T cell sequencing was performed using the Adaptive immunoseq platform as well as RNA-based TCR deep sequencing as previously described (PMID: 31219185)
immunotherapy, hematopoietic stem cell transplant, t cell, immunodeficiency
immunotherapy, hematopoietic stem cell transplant, t cell, immunodeficiency
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