Will Post-Transplantation Cell Therapies for Pediatric Patients Become Standard of Care?
Autor: | Lankester, A.C., Locatelli, F., Bader, P., Rettinger, E., Egeler, M., Katewa, S., Pulsipher, M.A., Nierkens, S., Schultz, K., Handgretinger, R., Grupp, S.A., Boelens, J.J., Bollard, C.M., Westhafen Intercontinental Grp |
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Jazyk: | angličtina |
Rok vydání: | 2015 |
Předmět: |
Graft Rejection
Male medicine.medical_treatment Adoptive cellular therapy Cell- and Tissue-Based Therapy Graft vs Host Disease Hematopoietic stem cell transplantation Disease Pediatrics NATURAL-KILLER-CELLS 0302 clinical medicine VERSUS-HOST-DISEASE Medicine Child 0303 health sciences Hematology Graft vs Tumor Effect adoptive cellular therapy chimeric antigen receptor pediatrics stem cell transplantation Hematopoietic Stem Cell Transplantation Stem cell transplantation ALLOGENEIC-DENDRITIC CELLS Allografts CHIMERIC ANTIGEN RECEPTOR 3. Good health surgical procedures operative Settore MED/38 - PEDIATRIA GENERALE E SPECIALISTICA Child Preschool Hematologic Neoplasms Lymphocyte Transfusion Female T-REGULATORY CELLS medicine.medical_specialty MINOR HISTOCOMPATIBILITY ANTIGENS Adolescent chemical and pharmacologic phenomena MESENCHYMAL STROMAL CELLS ACUTE MYELOID-LEUKEMIA Donor lymphocyte infusion 03 medical and health sciences Immune system Internal medicine Humans Intensive care medicine 030304 developmental biology ACUTE LYMPHOBLASTIC-LEUKEMIA Transplantation business.industry Mesenchymal stem cell Infant BONE-MARROW-TRANSPLANTATION Chimeric antigen receptor Immunology business 030215 immunology |
Zdroj: | Biology of Blood and Marrow Transplantation, 21(3), 402. Elsevier Inc. Biology of Blood and Marrow Transplantation, 21(3), 402-411 |
ISSN: | 1083-8791 |
Popis: | Although allogeneic hematopoietic stem cell transplantation (HSCT) is a curative approach for many pediatric patients with hematologic malignancies and some nonmalignant disorders, some critical obstacles remain to be overcome, including relapse, engraftment failure, graft-versus-host disease (GVHD), and infection. Harnessing the immune system to induce a graft-versus-tumor effect or rapidly restore antiviral immunity through the use of donor lymphocyte infusion (DLI) has been remarkably successful in some settings. Unfortunately, however, the responses to DLI can be variable, and GVHD is common. Thus, manipulations to minimize GVHD while restoring antiviral immunity and enhancing the graft-versus-tumor effect are needed to improve outcomes after allogeneic HSCT. Cellular therapies, defined as treatment modalities in which hematopoietic or nonhematopoietic cells are used as therapeutic agents, offer this promise for improving outcomes post-HSCT. This review presents an overview of the field for pediatric cell therapies in the transplant setting and discusses how we can broaden applicability beyond phase I. (C) 2015 American Society for Blood and Marrow Transplantation. |
Databáze: | OpenAIRE |
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