Targeting CLL-1 for acute myeloid leukemia therapy

Abstract Despite major scientific discoveries and novel therapies over the past four decades, the treatment outcomes of acute myeloid leukemia (AML), especially in the adult patient population remain dismal. In the past few years, an increasing number of targets such as CD33, CD123, CLL-1, CD47, CD7...

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Main Authors: Hongbing Ma, Iyer Swaminathan Padmanabhan, Simrit Parmar, Yuping Gong
Format: Article
Language:English
Published: BMC 2019-04-01
Series:Journal of Hematology & Oncology
Subjects:
Online Access:http://link.springer.com/article/10.1186/s13045-019-0726-5
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author Hongbing Ma
Iyer Swaminathan Padmanabhan
Simrit Parmar
Yuping Gong
author_facet Hongbing Ma
Iyer Swaminathan Padmanabhan
Simrit Parmar
Yuping Gong
author_sort Hongbing Ma
collection DOAJ
description Abstract Despite major scientific discoveries and novel therapies over the past four decades, the treatment outcomes of acute myeloid leukemia (AML), especially in the adult patient population remain dismal. In the past few years, an increasing number of targets such as CD33, CD123, CLL-1, CD47, CD70, and TIM3, have been developed for immunotherapy of AML. Among them, CLL-1 has attracted the researchers’ attention due to its high expression in AML while being absent in normal hematopoietic stem cell. Accumulating evidence have demonstrated CLL-1 is an ideal target for AML. In this paper, we will review the expression of CLL-1 on normal cells and AML, the value of CLL-1 in diagnosis and follow-up, and targeting CLL-1 therapy-based antibody and chimeric antigen receptor T cell therapy as well as providing an overview of CLL-1 as a target for AML.
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spelling doaj.art-676c89746d2741368482135227ee051c2022-12-22T00:49:51ZengBMCJournal of Hematology & Oncology1756-87222019-04-0112111110.1186/s13045-019-0726-5Targeting CLL-1 for acute myeloid leukemia therapyHongbing Ma0Iyer Swaminathan Padmanabhan1Simrit Parmar2Yuping Gong3Hematology Department, West China Hospital, Sichuan UniversityDepartment of Lymphoma and Myeloma, MD Anderson Cancer Center, Texas UniversityDepartment of Lymphoma and Myeloma, MD Anderson Cancer Center, Texas UniversityHematology Department, West China Hospital, Sichuan UniversityAbstract Despite major scientific discoveries and novel therapies over the past four decades, the treatment outcomes of acute myeloid leukemia (AML), especially in the adult patient population remain dismal. In the past few years, an increasing number of targets such as CD33, CD123, CLL-1, CD47, CD70, and TIM3, have been developed for immunotherapy of AML. Among them, CLL-1 has attracted the researchers’ attention due to its high expression in AML while being absent in normal hematopoietic stem cell. Accumulating evidence have demonstrated CLL-1 is an ideal target for AML. In this paper, we will review the expression of CLL-1 on normal cells and AML, the value of CLL-1 in diagnosis and follow-up, and targeting CLL-1 therapy-based antibody and chimeric antigen receptor T cell therapy as well as providing an overview of CLL-1 as a target for AML.http://link.springer.com/article/10.1186/s13045-019-0726-5Acute myeloid leukemiaCLL-1CLEC12ADCAL-2hMICLCD371
spellingShingle Hongbing Ma
Iyer Swaminathan Padmanabhan
Simrit Parmar
Yuping Gong
Targeting CLL-1 for acute myeloid leukemia therapy
Journal of Hematology & Oncology
Acute myeloid leukemia
CLL-1
CLEC12A
DCAL-2
hMICL
CD371
title Targeting CLL-1 for acute myeloid leukemia therapy
title_full Targeting CLL-1 for acute myeloid leukemia therapy
title_fullStr Targeting CLL-1 for acute myeloid leukemia therapy
title_full_unstemmed Targeting CLL-1 for acute myeloid leukemia therapy
title_short Targeting CLL-1 for acute myeloid leukemia therapy
title_sort targeting cll 1 for acute myeloid leukemia therapy
topic Acute myeloid leukemia
CLL-1
CLEC12A
DCAL-2
hMICL
CD371
url http://link.springer.com/article/10.1186/s13045-019-0726-5
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AT yupinggong targetingcll1foracutemyeloidleukemiatherapy