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Targeting CLL-1 for acute myeloid leukemia therapy

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 TI...

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Autores principales: Ma, Hongbing, Padmanabhan, Iyer Swaminathan, Parmar, Simrit, Gong, Yuping
Formato: Online Artículo Texto
Lenguaje:English
Publicado: BioMed Central 2019
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6480870/
https://www.ncbi.nlm.nih.gov/pubmed/31014360
http://dx.doi.org/10.1186/s13045-019-0726-5
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author Ma, Hongbing
Padmanabhan, Iyer Swaminathan
Parmar, Simrit
Gong, Yuping
author_facet Ma, Hongbing
Padmanabhan, Iyer Swaminathan
Parmar, Simrit
Gong, Yuping
author_sort Ma, Hongbing
collection PubMed
description 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 pubmed-64808702019-05-02 Targeting CLL-1 for acute myeloid leukemia therapy Ma, Hongbing Padmanabhan, Iyer Swaminathan Parmar, Simrit Gong, Yuping J Hematol Oncol Review 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. BioMed Central 2019-04-24 /pmc/articles/PMC6480870/ /pubmed/31014360 http://dx.doi.org/10.1186/s13045-019-0726-5 Text en © The Author(s). 2019 Open AccessThis article is distributed under the terms of the Creative Commons Attribution 4.0 International License (http://creativecommons.org/licenses/by/4.0/), which permits unrestricted use, distribution, and reproduction in any medium, provided you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons license, and indicate if changes were made. The Creative Commons Public Domain Dedication waiver (http://creativecommons.org/publicdomain/zero/1.0/) applies to the data made available in this article, unless otherwise stated.
spellingShingle Review
Ma, Hongbing
Padmanabhan, Iyer Swaminathan
Parmar, Simrit
Gong, Yuping
Targeting CLL-1 for acute myeloid leukemia therapy
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 Review
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6480870/
https://www.ncbi.nlm.nih.gov/pubmed/31014360
http://dx.doi.org/10.1186/s13045-019-0726-5
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