Donor origin CAR T cells: graft versus malignancy effect without GVHD, a systematic review

Immunotherapy. 2017 Jan;9(2):123-130. doi: 10.2217/imt-2016-0127.

Abstract

CD19, CD20 chimeric antigen receptor T (CAR T) cell therapy has shown promising results for the treatment of relapsed or refractory hematological malignancies. Best results have been reported in acute lymphoblastic leukemia patients with a complete response rate above 80%. Patients who received donor-derived CAR T cells for the relapsed malignancy after stem cell transplantation (allogenic hematopoietic stem cell transplant) were identified from the published trials. A total of 72 patients from seven studies were treated with donor-derived CAR T cells. Only five out of 72 patients (6.9%) developed graft versus host disease. Use of donor-derived CAR T cell for relapse prophylaxis, minimal residual disease clearance or salvage from relapse is therefore highly effective, and risk of graft versus host disease flare is very low. Side effects include cytokine release syndrome, tumor lysis syndrome, B-cell aplasia along with CNS toxicity.

Keywords: allogenic stem cell transplantation; chimeric antigen T cells; graft versus leukemia; hematological malignancy; relapse; salvage.

Publication types

  • Meta-Analysis
  • Review
  • Systematic Review

MeSH terms

  • Animals
  • Antigens, CD19 / immunology
  • Antigens, CD20 / immunology
  • Graft vs Host Disease / immunology*
  • Graft vs Tumor Effect / immunology*
  • Hematologic Neoplasms / immunology
  • Hematologic Neoplasms / therapy*
  • Hematopoietic Stem Cell Transplantation*
  • Humans
  • Immunotherapy, Adoptive / methods*
  • Receptors, Antigen, T-Cell / genetics
  • Receptors, Antigen, T-Cell / metabolism*
  • Recombinant Fusion Proteins / genetics
  • Recurrence
  • T-Lymphocytes / immunology*
  • T-Lymphocytes / transplantation
  • Tissue Donors
  • Transplantation, Homologous

Substances

  • Antigens, CD19
  • Antigens, CD20
  • Receptors, Antigen, T-Cell
  • Recombinant Fusion Proteins