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Preclinical evaluation of CD70-specific CAR T cells targeting acute myeloid leukemia
BACKGROUNDS: Chimeric antigen receptor (CAR)-T cell therapy has achieved unprecedented success in treating hematopoietic malignancies. However, this cell therapy is hampered in treating acute myeloid leukemia (AML) due to lack of ideal cell surface targets that only express on AML blasts and leukemi...
Autores principales: | , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Frontiers Media S.A.
2023
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9950117/ https://www.ncbi.nlm.nih.gov/pubmed/36845088 http://dx.doi.org/10.3389/fimmu.2023.1093750 |
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author | Wu, Gongqiang Guo, Shanshan Luo, Qian Wang, Xiaoxia Deng, Wenhai Ouyang, Guifang Pu, Jeffrey J. Lei, Wen Qian, Wenbin |
author_facet | Wu, Gongqiang Guo, Shanshan Luo, Qian Wang, Xiaoxia Deng, Wenhai Ouyang, Guifang Pu, Jeffrey J. Lei, Wen Qian, Wenbin |
author_sort | Wu, Gongqiang |
collection | PubMed |
description | BACKGROUNDS: Chimeric antigen receptor (CAR)-T cell therapy has achieved unprecedented success in treating hematopoietic malignancies. However, this cell therapy is hampered in treating acute myeloid leukemia (AML) due to lack of ideal cell surface targets that only express on AML blasts and leukemia stem cells (LSCs) but not on normal hematopoietic stem cells (HSCs). METHODS: We detected the CD70 expression on the surfaces of AML cell lines, primary AML cells, HSC, and peripheral blood cells and generated a second-generation CD70-specific CAR-T cells using a construct containing a humanized 41D12-based scFv and a 41BB-CD3ζ intracellular signaling domain. Cytotoxicity, cytokine release, and proliferation in antigen stimulation, CD107a assay, and CFSE assays were used to demonstrate the potent anti-leukemia activity in vitro. A Molm-13 xenograft mouse model was established to evaluate the anti-leukemic activity of CD70 CAR-T in vivo. CFU assay was explored to assess the safety of CD70 CAR-T on HSC. RESULTS: CD70 heterogeneously expressed on AML primary cells, including leukemia blasts, leukemic progenitor, and stem cells, but not expressed on normal HSCs and majority of blood cells. Anti-CD70 CAR-T cells exhibited potent cytotoxicity, cytokines production, and proliferation when incubated with CD70(+) AML cell lines. It also displayed robust anti-leukemia activity and prolonged survival in Molm-13 xenograft mouse model. However, such CAR-T cell therapy did not completely eliminate leukemia in vivo. DISCUSSION: Our study reveals that anti-CD70 CAR-T cells are a new potential treatment for AML. However, such CAR-T cell therapy did not completely eliminate leukemia in vivo, suggesting that future studies aiming to generate innovative combinatorial CAR constructs or to increase CD70 expression density on leukemia cell surface to prolong the life-span of CAR-T cells in the circulation will be needed in order to optimize CAR-T cell responses for AML. |
format | Online Article Text |
id | pubmed-9950117 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2023 |
publisher | Frontiers Media S.A. |
record_format | MEDLINE/PubMed |
spelling | pubmed-99501172023-02-25 Preclinical evaluation of CD70-specific CAR T cells targeting acute myeloid leukemia Wu, Gongqiang Guo, Shanshan Luo, Qian Wang, Xiaoxia Deng, Wenhai Ouyang, Guifang Pu, Jeffrey J. Lei, Wen Qian, Wenbin Front Immunol Immunology BACKGROUNDS: Chimeric antigen receptor (CAR)-T cell therapy has achieved unprecedented success in treating hematopoietic malignancies. However, this cell therapy is hampered in treating acute myeloid leukemia (AML) due to lack of ideal cell surface targets that only express on AML blasts and leukemia stem cells (LSCs) but not on normal hematopoietic stem cells (HSCs). METHODS: We detected the CD70 expression on the surfaces of AML cell lines, primary AML cells, HSC, and peripheral blood cells and generated a second-generation CD70-specific CAR-T cells using a construct containing a humanized 41D12-based scFv and a 41BB-CD3ζ intracellular signaling domain. Cytotoxicity, cytokine release, and proliferation in antigen stimulation, CD107a assay, and CFSE assays were used to demonstrate the potent anti-leukemia activity in vitro. A Molm-13 xenograft mouse model was established to evaluate the anti-leukemic activity of CD70 CAR-T in vivo. CFU assay was explored to assess the safety of CD70 CAR-T on HSC. RESULTS: CD70 heterogeneously expressed on AML primary cells, including leukemia blasts, leukemic progenitor, and stem cells, but not expressed on normal HSCs and majority of blood cells. Anti-CD70 CAR-T cells exhibited potent cytotoxicity, cytokines production, and proliferation when incubated with CD70(+) AML cell lines. It also displayed robust anti-leukemia activity and prolonged survival in Molm-13 xenograft mouse model. However, such CAR-T cell therapy did not completely eliminate leukemia in vivo. DISCUSSION: Our study reveals that anti-CD70 CAR-T cells are a new potential treatment for AML. However, such CAR-T cell therapy did not completely eliminate leukemia in vivo, suggesting that future studies aiming to generate innovative combinatorial CAR constructs or to increase CD70 expression density on leukemia cell surface to prolong the life-span of CAR-T cells in the circulation will be needed in order to optimize CAR-T cell responses for AML. Frontiers Media S.A. 2023-02-10 /pmc/articles/PMC9950117/ /pubmed/36845088 http://dx.doi.org/10.3389/fimmu.2023.1093750 Text en Copyright © 2023 Wu, Guo, Luo, Wang, Deng, Ouyang, Pu, Lei and Qian https://creativecommons.org/licenses/by/4.0/This is an open-access article distributed under the terms of the Creative Commons Attribution License (CC BY). The use, distribution or reproduction in other forums is permitted, provided the original author(s) and the copyright owner(s) are credited and that the original publication in this journal is cited, in accordance with accepted academic practice. No use, distribution or reproduction is permitted which does not comply with these terms. |
spellingShingle | Immunology Wu, Gongqiang Guo, Shanshan Luo, Qian Wang, Xiaoxia Deng, Wenhai Ouyang, Guifang Pu, Jeffrey J. Lei, Wen Qian, Wenbin Preclinical evaluation of CD70-specific CAR T cells targeting acute myeloid leukemia |
title | Preclinical evaluation of CD70-specific CAR T cells targeting acute myeloid leukemia |
title_full | Preclinical evaluation of CD70-specific CAR T cells targeting acute myeloid leukemia |
title_fullStr | Preclinical evaluation of CD70-specific CAR T cells targeting acute myeloid leukemia |
title_full_unstemmed | Preclinical evaluation of CD70-specific CAR T cells targeting acute myeloid leukemia |
title_short | Preclinical evaluation of CD70-specific CAR T cells targeting acute myeloid leukemia |
title_sort | preclinical evaluation of cd70-specific car t cells targeting acute myeloid leukemia |
topic | Immunology |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9950117/ https://www.ncbi.nlm.nih.gov/pubmed/36845088 http://dx.doi.org/10.3389/fimmu.2023.1093750 |
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