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- [2] Feasibility and Efficacy of CD45RA+Depleted Donor Lymphocytes Infusion After Haploidentical Transplantation With Post-Transplantation Cyclophosphamide in Patients With Hematological Malignancies TRANSPLANTATION AND CELLULAR THERAPY, 2021, 27 (06): : 478.e1 - 478.e5
- [5] Haploidentical T Cell-Replete Transplantation with Post-Transplantation Cyclophosphamide for Patients in or above the Sixth Decade of Age Compared with Allogeneic Hematopoietic Stem Cell Transplantation from an Human Leukocyte Antigen-Matched Related or Unrelated Donor BIOLOGY OF BLOOD AND MARROW TRANSPLANTATION, 2016, 22 (01) : 119 - 124
- [6] CD56-enriched donor cell infusion after post-transplantation cyclophosphamide for haploidentical transplantation of advanced myeloid malignancies is associated with prompt reconstitution of mature natural killer cells and regulatory T cells with reduced incidence of acute graft versus host disease: A pilot study CYTOTHERAPY, 2017, 19 (04) : 531 - 542
- [7] Early and sequential CTLA4Ig primed donor lymphocyte infusions (DLI) following post-transplantation cyclophosphamide (PTCY)-based haploidentical PBSC transplantation for advanced hematological malignancies promote proliferation of mature natural killer (NK) cells with cytotoxic potential and markedly reduces relapse-risk without increase in GVHD BONE MARROW TRANSPLANTATION, 2017, 52 : S154 - S154
- [8] Direct Integration of Anti-CD19 Chimeric-Antigen-Receptor (CAR) T Cells Early after Post-Transplantation Cyclophosphamide (PTCy) in Murine MHC-Haploidentical Hematopoietic Cell Transplantation (HCT) Exerts Anti-Tumor Effects without Causing Graft-Versus-Host Disease (GVHD) BIOLOGY OF BLOOD AND MARROW TRANSPLANTATION, 2020, 26 (03) : S170 - S171
- [9] NK-cell alloreactivity based on KIR/ligand mismatch in the donor vs recipient direction provides better graft-versus-tumor effect in patients with active hematological malignancies undergoing allogeneic T-replete haploidentical transplantation followed by post-transplant cyclophosphamide BONE MARROW TRANSPLANTATION, 2017, 52 : S186 - S186