Current status of immunotherapy in acute myeloid leukemia

Acute myeloid leukemia (AML) is a rapidly progressive, poor prognosis malignant tumor caused by hematopoietic stem cells/progenitor cells. In recent years, there have been significant advances in basic and preclinical research on AML. Compared with traditional chemotherapy, hematopoietic stem cell t...

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Main Author: Li Wenrui
Format: Article
Language:English
Published: EDP Sciences 2021-01-01
Series:E3S Web of Conferences
Online Access:https://www.e3s-conferences.org/articles/e3sconf/pdf/2021/47/e3sconf_icepe2021_03025.pdf
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spelling doaj-8532a8af859c4d2fa961240eab88ea432021-06-18T08:20:28ZengEDP SciencesE3S Web of Conferences2267-12422021-01-012710302510.1051/e3sconf/202127103025e3sconf_icepe2021_03025Current status of immunotherapy in acute myeloid leukemiaLi Wenrui0Department of Pathophysiology, Key Laboratory of Cell Differentiation and Apoptosis, Shanghai Jiao Tong University School of MedicineAcute myeloid leukemia (AML) is a rapidly progressive, poor prognosis malignant tumor caused by hematopoietic stem cells/progenitor cells. In recent years, there have been significant advances in basic and preclinical research on AML. Compared with traditional chemotherapy, hematopoietic stem cell transplantation (HSCT) significantly improved prognosis. However, with high recurrence rates and low 5-year survival rates, more and more attention has been focused on immunotherapy strategies for AML. Given the immunological characteristics of AML and the mechanisms of immune escape, ongoing efforts are aimed at improving the strategy of immunotherapy and the design of novel therapies, such as vaccines, monoclonal antibodies, chimeric receptor-engineered T cells (CAR-T), and checkpoint inhibitors, which hopefully can deliver higher specificity and efficacy in AML therapy. In this review, we provide an overview of the immunological characteristics of conventional AML therapies, explore immune avoidance mechanisms, and describe the mechanisms of active and passive immunotherapies and current clinical trials.https://www.e3s-conferences.org/articles/e3sconf/pdf/2021/47/e3sconf_icepe2021_03025.pdf
collection DOAJ
language English
format Article
sources DOAJ
author Li Wenrui
spellingShingle Li Wenrui
Current status of immunotherapy in acute myeloid leukemia
E3S Web of Conferences
author_facet Li Wenrui
author_sort Li Wenrui
title Current status of immunotherapy in acute myeloid leukemia
title_short Current status of immunotherapy in acute myeloid leukemia
title_full Current status of immunotherapy in acute myeloid leukemia
title_fullStr Current status of immunotherapy in acute myeloid leukemia
title_full_unstemmed Current status of immunotherapy in acute myeloid leukemia
title_sort current status of immunotherapy in acute myeloid leukemia
publisher EDP Sciences
series E3S Web of Conferences
issn 2267-1242
publishDate 2021-01-01
description Acute myeloid leukemia (AML) is a rapidly progressive, poor prognosis malignant tumor caused by hematopoietic stem cells/progenitor cells. In recent years, there have been significant advances in basic and preclinical research on AML. Compared with traditional chemotherapy, hematopoietic stem cell transplantation (HSCT) significantly improved prognosis. However, with high recurrence rates and low 5-year survival rates, more and more attention has been focused on immunotherapy strategies for AML. Given the immunological characteristics of AML and the mechanisms of immune escape, ongoing efforts are aimed at improving the strategy of immunotherapy and the design of novel therapies, such as vaccines, monoclonal antibodies, chimeric receptor-engineered T cells (CAR-T), and checkpoint inhibitors, which hopefully can deliver higher specificity and efficacy in AML therapy. In this review, we provide an overview of the immunological characteristics of conventional AML therapies, explore immune avoidance mechanisms, and describe the mechanisms of active and passive immunotherapies and current clinical trials.
url https://www.e3s-conferences.org/articles/e3sconf/pdf/2021/47/e3sconf_icepe2021_03025.pdf
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