VISTA in hematological malignancies: a review of the literature

In recent years, tumor immunotherapy has become an active research area, with the emergence of immune checkpoint inhibitors (ICIs) revolutionizing immunotherapy. Clinical evidence indicates that programmed cell death protein 1 (PD-1) monoclonal antibodies and other drugs have remarkable therapeutic...

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Main Authors: Yuanjia Duan, Xiaotong Ren, Xinyu Guo, Jiayi Xie, Zhaoyun Liu, Lijuan Li
Format: Article
Language:English
Published: Frontiers Media S.A. 2024-12-01
Series:Frontiers in Immunology
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Online Access:https://www.frontiersin.org/articles/10.3389/fimmu.2024.1466839/full
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author Yuanjia Duan
Yuanjia Duan
Yuanjia Duan
Xiaotong Ren
Xiaotong Ren
Xiaotong Ren
Xinyu Guo
Xinyu Guo
Xinyu Guo
Jiayi Xie
Jiayi Xie
Jiayi Xie
Zhaoyun Liu
Zhaoyun Liu
Zhaoyun Liu
Lijuan Li
Lijuan Li
Lijuan Li
author_facet Yuanjia Duan
Yuanjia Duan
Yuanjia Duan
Xiaotong Ren
Xiaotong Ren
Xiaotong Ren
Xinyu Guo
Xinyu Guo
Xinyu Guo
Jiayi Xie
Jiayi Xie
Jiayi Xie
Zhaoyun Liu
Zhaoyun Liu
Zhaoyun Liu
Lijuan Li
Lijuan Li
Lijuan Li
author_sort Yuanjia Duan
collection DOAJ
description In recent years, tumor immunotherapy has become an active research area, with the emergence of immune checkpoint inhibitors (ICIs) revolutionizing immunotherapy. Clinical evidence indicates that programmed cell death protein 1 (PD-1) monoclonal antibodies and other drugs have remarkable therapeutic effects. V-domain Ig suppressor of T-cell activation (VISTA) is a new type of immune checkpoint receptor that is highly expressed in various tumors. It is co-expressed with PD-1, T-cell immunoglobulin domain, mucin domain-3 (Tim-3), T-cell immunoglobulin, and immunoreceptor tyrosine-based inhibitory motif domain (TIGIT) and is associated with prognosis, which suggests that it may be a target for immunotherapy. As an immune checkpoint receptor with no mature drugs, VISTA is highly expressed in acute myeloid leukemia (AML), multiple myeloma (MM), and other hematological malignancies; however, its pathogenic mechanism should be defined to better guide treatment.
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institution Kabale University
issn 1664-3224
language English
publishDate 2024-12-01
publisher Frontiers Media S.A.
record_format Article
series Frontiers in Immunology
spelling doaj-art-a5e4ce537ab94a77a259d9e17493c9d12024-12-17T06:23:23ZengFrontiers Media S.A.Frontiers in Immunology1664-32242024-12-011510.3389/fimmu.2024.14668391466839VISTA in hematological malignancies: a review of the literatureYuanjia Duan0Yuanjia Duan1Yuanjia Duan2Xiaotong Ren3Xiaotong Ren4Xiaotong Ren5Xinyu Guo6Xinyu Guo7Xinyu Guo8Jiayi Xie9Jiayi Xie10Jiayi Xie11Zhaoyun Liu12Zhaoyun Liu13Zhaoyun Liu14Lijuan Li15Lijuan Li16Lijuan Li17Department of Hematology, Tianjin Medical University General Hospital, Tianjin, ChinaTianjin Key Laboratory of Bone Marrow Failure and Malignant Hemopoietic Clone Control, Tianjin, ChinaTianjin Institute of Hematology, Tianjin, ChinaDepartment of Hematology, Tianjin Medical University General Hospital, Tianjin, ChinaTianjin Key Laboratory of Bone Marrow Failure and Malignant Hemopoietic Clone Control, Tianjin, ChinaTianjin Institute of Hematology, Tianjin, ChinaDepartment of Hematology, Tianjin Medical University General Hospital, Tianjin, ChinaTianjin Key Laboratory of Bone Marrow Failure and Malignant Hemopoietic Clone Control, Tianjin, ChinaTianjin Institute of Hematology, Tianjin, ChinaDepartment of Hematology, Tianjin Medical University General Hospital, Tianjin, ChinaTianjin Key Laboratory of Bone Marrow Failure and Malignant Hemopoietic Clone Control, Tianjin, ChinaTianjin Institute of Hematology, Tianjin, ChinaDepartment of Hematology, Tianjin Medical University General Hospital, Tianjin, ChinaTianjin Key Laboratory of Bone Marrow Failure and Malignant Hemopoietic Clone Control, Tianjin, ChinaTianjin Institute of Hematology, Tianjin, ChinaDepartment of Hematology, Tianjin Medical University General Hospital, Tianjin, ChinaTianjin Key Laboratory of Bone Marrow Failure and Malignant Hemopoietic Clone Control, Tianjin, ChinaTianjin Institute of Hematology, Tianjin, ChinaIn recent years, tumor immunotherapy has become an active research area, with the emergence of immune checkpoint inhibitors (ICIs) revolutionizing immunotherapy. Clinical evidence indicates that programmed cell death protein 1 (PD-1) monoclonal antibodies and other drugs have remarkable therapeutic effects. V-domain Ig suppressor of T-cell activation (VISTA) is a new type of immune checkpoint receptor that is highly expressed in various tumors. It is co-expressed with PD-1, T-cell immunoglobulin domain, mucin domain-3 (Tim-3), T-cell immunoglobulin, and immunoreceptor tyrosine-based inhibitory motif domain (TIGIT) and is associated with prognosis, which suggests that it may be a target for immunotherapy. As an immune checkpoint receptor with no mature drugs, VISTA is highly expressed in acute myeloid leukemia (AML), multiple myeloma (MM), and other hematological malignancies; however, its pathogenic mechanism should be defined to better guide treatment.https://www.frontiersin.org/articles/10.3389/fimmu.2024.1466839/fullimmune checkpoint receptorsVISTAhematological malignanciestumor microenvironmentimmunotherapy
spellingShingle Yuanjia Duan
Yuanjia Duan
Yuanjia Duan
Xiaotong Ren
Xiaotong Ren
Xiaotong Ren
Xinyu Guo
Xinyu Guo
Xinyu Guo
Jiayi Xie
Jiayi Xie
Jiayi Xie
Zhaoyun Liu
Zhaoyun Liu
Zhaoyun Liu
Lijuan Li
Lijuan Li
Lijuan Li
VISTA in hematological malignancies: a review of the literature
Frontiers in Immunology
immune checkpoint receptors
VISTA
hematological malignancies
tumor microenvironment
immunotherapy
title VISTA in hematological malignancies: a review of the literature
title_full VISTA in hematological malignancies: a review of the literature
title_fullStr VISTA in hematological malignancies: a review of the literature
title_full_unstemmed VISTA in hematological malignancies: a review of the literature
title_short VISTA in hematological malignancies: a review of the literature
title_sort vista in hematological malignancies a review of the literature
topic immune checkpoint receptors
VISTA
hematological malignancies
tumor microenvironment
immunotherapy
url https://www.frontiersin.org/articles/10.3389/fimmu.2024.1466839/full
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