TY - CHAP M1 - Book, Section TI - Cellular Therapy in Allogeneic Hematopoietic Cell Transplantation A1 - Olson, Amanda A1 - Ramdial, Jeremy A1 - Greenbaum, Uri A1 - Lin, Paul A1 - Rezvani, Katayoun A1 - Kebriaei, Partow A2 - Kantarjian, Hagop M. A2 - Wolff, Robert A. A2 - Rieber, Alyssa G. PY - 2022 T2 - The MD Anderson Manual of Medical Oncology, 4e AB - KEY CONCEPTSThe efficacy of allogeneic hematopoietic cell transplantation (HCT) is based on the graft-versus-tumor effect, by which the donor immune system achieves immunologic control of the tumor via the human leukocyte antigen (HLA) system.Three key barriers to successful HCT are relapse caused by failure of immunologic control of the underlying disease, graft-versus-host disease (GVHD), and infectious complications, and studies are underway to improve on these complications.Strategies to mitigate relapse include using prophylactic donor lymphocyte infusions, chimeric antigen receptor modified T-cells derived typically from the patient, and natural killer (NK) T-cells.In contrast to B and T lymphocytes, NK T-cells do not express rearranged, antigen-specific receptors and as a consequence have a low risk for GVHD, allowing the use of allogeneic NK cells. An allogeneic product is advantageous because it is readily available and furthermore uses healthy immune cells for product production.The pathogenesis of GVHD is complex and includes the differentiation of naïve donor T-cells into effector cells that attack host tissues. Increasing numbers of HLA misma tches are associated with higher incidence of GVHD and transplant-related mortality. Grades II to IV acute GVHD occur in 25% to 60% of cases with matched related donors and 45% to 70% of cases with matched unrelated donors. Recent improvements in GVHD include the approval of ruxolitinib for steroid-refractory acute GVHD and the use of posttransplant cyclophosphamide to decrease the incidence of GVHD.Viral infection is a major cause of death after HCT, resulting from cellular and humoral immune deficiency. Viral infections of particular relevance after HCT are cytomegalovirus, Epstein-Barr virus, the polyoma viruses BK and JC, adenovirus, and human herpesvirus 6. Pharmacotherapy for these infections has limited efficacy. Viral-specific T-cells directed against these infections is feasible to generate and effective. SN - PB - McGraw Hill Education CY - New York, NY Y2 - 2024/04/19 UR - hemonc.mhmedical.com/content.aspx?aid=1190834149 ER -