The Graft-Versus-Leukemia Effect in AML

Allogeneic hematopoietic stem cell transplantation (allo-SCT) is the most established and commonly used cellular immunotherapy in cancer care. It is the most potent anti-leukemic therapy in patients with acute myeloid leukemia (AML) and is routinely used with curative intent in patients with interme...

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Main Authors: Connor Sweeney, Paresh Vyas
Format: Article
Language:English
Published: Frontiers Media S.A. 2019-11-01
Series:Frontiers in Oncology
Subjects:
Online Access:https://www.frontiersin.org/article/10.3389/fonc.2019.01217/full
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author Connor Sweeney
Connor Sweeney
Paresh Vyas
Paresh Vyas
author_facet Connor Sweeney
Connor Sweeney
Paresh Vyas
Paresh Vyas
author_sort Connor Sweeney
collection DOAJ
description Allogeneic hematopoietic stem cell transplantation (allo-SCT) is the most established and commonly used cellular immunotherapy in cancer care. It is the most potent anti-leukemic therapy in patients with acute myeloid leukemia (AML) and is routinely used with curative intent in patients with intermediate and poor risk disease. Donor T cells, and possibly other immune cells, eliminate residual leukemia cells after prior (radio)chemotherapy. This immune-mediated response is known as graft-versus-leukemia (GvL). Donor alloimmune responses can also be directed against healthy tissues, which is known as graft-versus-host disease (GvHD). GvHD and GvL often co-occur and, therefore, a major barrier to exploiting the full immunotherapeutic benefit of donor immune cells against patient leukemia is the immunosuppression required to treat GvHD. However, curative responses to allo-SCT and GvHD do not always occur together, suggesting that these two immune responses could be de-coupled in some patients. To make further progress in successfully promoting GvL without GvHD, we must transform our limited understanding of the cellular and molecular basis of GvL and GvHD. Specifically, in most patients we do not understand the antigenic basis of immune responses in GvL and GvHD. Identification of antigens important for GvL but not GvHD, and vice versa, could impact on donor selection, allow us to track GvL immune responses and begin to specifically harness and strengthen anti-leukemic immune responses against patient AML cells, whilst minimizing the toxicity of GvHD.
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spelling doaj.art-dde754b237b74550b873cdc5d22a73222022-12-21T23:41:12ZengFrontiers Media S.A.Frontiers in Oncology2234-943X2019-11-01910.3389/fonc.2019.01217493111The Graft-Versus-Leukemia Effect in AMLConnor Sweeney0Connor Sweeney1Paresh Vyas2Paresh Vyas3MRC Molecular Haematology Unit, Oxford Biomedical Research Centre, MRC Weatherall Institute of Molecular Medicine, University of Oxford, Oxford, United KingdomDepartment of Haematology, Oxford University Hospitals NHS Foundation Trust, Oxford, United KingdomMRC Molecular Haematology Unit, Oxford Biomedical Research Centre, MRC Weatherall Institute of Molecular Medicine, University of Oxford, Oxford, United KingdomDepartment of Haematology, Oxford University Hospitals NHS Foundation Trust, Oxford, United KingdomAllogeneic hematopoietic stem cell transplantation (allo-SCT) is the most established and commonly used cellular immunotherapy in cancer care. It is the most potent anti-leukemic therapy in patients with acute myeloid leukemia (AML) and is routinely used with curative intent in patients with intermediate and poor risk disease. Donor T cells, and possibly other immune cells, eliminate residual leukemia cells after prior (radio)chemotherapy. This immune-mediated response is known as graft-versus-leukemia (GvL). Donor alloimmune responses can also be directed against healthy tissues, which is known as graft-versus-host disease (GvHD). GvHD and GvL often co-occur and, therefore, a major barrier to exploiting the full immunotherapeutic benefit of donor immune cells against patient leukemia is the immunosuppression required to treat GvHD. However, curative responses to allo-SCT and GvHD do not always occur together, suggesting that these two immune responses could be de-coupled in some patients. To make further progress in successfully promoting GvL without GvHD, we must transform our limited understanding of the cellular and molecular basis of GvL and GvHD. Specifically, in most patients we do not understand the antigenic basis of immune responses in GvL and GvHD. Identification of antigens important for GvL but not GvHD, and vice versa, could impact on donor selection, allow us to track GvL immune responses and begin to specifically harness and strengthen anti-leukemic immune responses against patient AML cells, whilst minimizing the toxicity of GvHD.https://www.frontiersin.org/article/10.3389/fonc.2019.01217/fullacute myeloid leukemiastem cell transplantationgraft-versus-leukemiagraft-versus-host diseaseT cellsantigens
spellingShingle Connor Sweeney
Connor Sweeney
Paresh Vyas
Paresh Vyas
The Graft-Versus-Leukemia Effect in AML
Frontiers in Oncology
acute myeloid leukemia
stem cell transplantation
graft-versus-leukemia
graft-versus-host disease
T cells
antigens
title The Graft-Versus-Leukemia Effect in AML
title_full The Graft-Versus-Leukemia Effect in AML
title_fullStr The Graft-Versus-Leukemia Effect in AML
title_full_unstemmed The Graft-Versus-Leukemia Effect in AML
title_short The Graft-Versus-Leukemia Effect in AML
title_sort graft versus leukemia effect in aml
topic acute myeloid leukemia
stem cell transplantation
graft-versus-leukemia
graft-versus-host disease
T cells
antigens
url https://www.frontiersin.org/article/10.3389/fonc.2019.01217/full
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