Figure 6
Figure 6. Poor expansion of adoptively transferred memory T cells in the absence of cognate antigen. (A) MHC class I tetramer identification of CD8+ T cells specific for Flu IK9 and Flu GL9 epitopes in the PB of marrow donors and the related recipients (R) at day 90 post–haplo-HSCT. (B) TNF and IFN-γ production by CD4+ and CD8+ T cells from the haplo-HSCT #10 donor/recipient pair (CMV+ and CMV−, respectively) following in vitro stimulation with CMV pp65 peptide pool. In panels A and B, numbers indicate the percentage of cells identified by the gates. (C) Summary of the frequency of CD3+ natural killer T cells binding CD1d/PBS57 tetramer and Flu and CMV-specific CD4+ and CD8+ T cells from the PB of donor (D) and the related recipients (R) at day (d) 45 and d90 post–haplo-HSCT. *P < .05, Mann-Whitney test. (D) Differentiation phenotypes of the transferred antigen-specific T cells identified in panel C. Data are presented relative to total memory T cells.

Poor expansion of adoptively transferred memory T cells in the absence of cognate antigen. (A) MHC class I tetramer identification of CD8+ T cells specific for Flu IK9 and Flu GL9 epitopes in the PB of marrow donors and the related recipients (R) at day 90 post–haplo-HSCT. (B) TNF and IFN-γ production by CD4+ and CD8+ T cells from the haplo-HSCT #10 donor/recipient pair (CMV+ and CMV, respectively) following in vitro stimulation with CMV pp65 peptide pool. In panels A and B, numbers indicate the percentage of cells identified by the gates. (C) Summary of the frequency of CD3+ natural killer T cells binding CD1d/PBS57 tetramer and Flu and CMV-specific CD4+ and CD8+ T cells from the PB of donor (D) and the related recipients (R) at day (d) 45 and d90 post–haplo-HSCT. *P < .05, Mann-Whitney test. (D) Differentiation phenotypes of the transferred antigen-specific T cells identified in panel C. Data are presented relative to total memory T cells.

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