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Assessment of the presence and anti-tumor potential of tumor-infiltrating lymphocytes in patients with acute myeloid leukemia

Purpose: Assessing the possibility of finding tumor-infiltrating lymphocytes (TIL) in bone marrow of acute myeloid leukemia (AML) patients and evaluating the anti-tumor activity of these TIL against autologous AML cells. Patients and methods: TIL were immunomagnetically isolated by using anti-CD3 fr...

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Autores principales: Wei, Liya, Wang, Zhenkun, Zhang, Zhuo, Li, Yinghua, Fan, Shengjin, Zhao, Yanqiu, Liu, Zhiyu, Ye, Xiangmei, Zhang, Fan, Yu, Yingying, Liu, Xiaolong, Cao, Fenglin, Zhou, Jin
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Dove 2019
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6489577/
https://www.ncbi.nlm.nih.gov/pubmed/31114360
http://dx.doi.org/10.2147/CMAR.S199817
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author Wei, Liya
Wang, Zhenkun
Zhang, Zhuo
Li, Yinghua
Fan, Shengjin
Zhao, Yanqiu
Liu, Zhiyu
Ye, Xiangmei
Zhang, Fan
Yu, Yingying
Liu, Xiaolong
Cao, Fenglin
Zhou, Jin
author_facet Wei, Liya
Wang, Zhenkun
Zhang, Zhuo
Li, Yinghua
Fan, Shengjin
Zhao, Yanqiu
Liu, Zhiyu
Ye, Xiangmei
Zhang, Fan
Yu, Yingying
Liu, Xiaolong
Cao, Fenglin
Zhou, Jin
author_sort Wei, Liya
collection PubMed
description Purpose: Assessing the possibility of finding tumor-infiltrating lymphocytes (TIL) in bone marrow of acute myeloid leukemia (AML) patients and evaluating the anti-tumor activity of these TIL against autologous AML cells. Patients and methods: TIL were immunomagnetically isolated by using anti-CD3 from bone marrow samples of 20 patients at the presentation of AML or four weeks upon completion of chemotherapy. TIL were ex vivo expanded for two weeks and immunophenotyped. Functionality in terms of cytokine secretion and cytotoxicity was assessed by γ-interferon quantitation and Elispot assay, respectively. Results: TIL were detected in bone marrow samples of 50% (10/20) of the patient cohort. They were noted to highly express CD137 and PD-1 and display a significantly higher anti-tumor reactivity compared to that of autologous peripheral blood lymphocytes. TIL could be expanded in co-cultures with irradiated feeder cells supplemented with interleukin (IL)-7 and IL-15. Conclusion: Data suggested the presence of reactive γ-interferon-secreting TIL in AML patients. They are expandable and possess anti-tumor activity, which might have a great potential in the development of adoptive cellular therapy for AML.
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spelling pubmed-64895772019-05-21 Assessment of the presence and anti-tumor potential of tumor-infiltrating lymphocytes in patients with acute myeloid leukemia Wei, Liya Wang, Zhenkun Zhang, Zhuo Li, Yinghua Fan, Shengjin Zhao, Yanqiu Liu, Zhiyu Ye, Xiangmei Zhang, Fan Yu, Yingying Liu, Xiaolong Cao, Fenglin Zhou, Jin Cancer Manag Res Original Research Purpose: Assessing the possibility of finding tumor-infiltrating lymphocytes (TIL) in bone marrow of acute myeloid leukemia (AML) patients and evaluating the anti-tumor activity of these TIL against autologous AML cells. Patients and methods: TIL were immunomagnetically isolated by using anti-CD3 from bone marrow samples of 20 patients at the presentation of AML or four weeks upon completion of chemotherapy. TIL were ex vivo expanded for two weeks and immunophenotyped. Functionality in terms of cytokine secretion and cytotoxicity was assessed by γ-interferon quantitation and Elispot assay, respectively. Results: TIL were detected in bone marrow samples of 50% (10/20) of the patient cohort. They were noted to highly express CD137 and PD-1 and display a significantly higher anti-tumor reactivity compared to that of autologous peripheral blood lymphocytes. TIL could be expanded in co-cultures with irradiated feeder cells supplemented with interleukin (IL)-7 and IL-15. Conclusion: Data suggested the presence of reactive γ-interferon-secreting TIL in AML patients. They are expandable and possess anti-tumor activity, which might have a great potential in the development of adoptive cellular therapy for AML. Dove 2019-04-12 /pmc/articles/PMC6489577/ /pubmed/31114360 http://dx.doi.org/10.2147/CMAR.S199817 Text en © 2019 Wei et al. http://creativecommons.org/licenses/by-nc/3.0/ This work is published and licensed by Dove Medical Press Limited. The full terms of this license are available at https://www.dovepress.com/terms.php and incorporate the Creative Commons Attribution – Non Commercial (unported, v3.0) License (http://creativecommons.org/licenses/by-nc/3.0/). By accessing the work you hereby accept the Terms. Non-commercial uses of the work are permitted without any further permission from Dove Medical Press Limited, provided the work is properly attributed. For permission for commercial use of this work, please see paragraphs 4.2 and 5 of our Terms (https://www.dovepress.com/terms.php).
spellingShingle Original Research
Wei, Liya
Wang, Zhenkun
Zhang, Zhuo
Li, Yinghua
Fan, Shengjin
Zhao, Yanqiu
Liu, Zhiyu
Ye, Xiangmei
Zhang, Fan
Yu, Yingying
Liu, Xiaolong
Cao, Fenglin
Zhou, Jin
Assessment of the presence and anti-tumor potential of tumor-infiltrating lymphocytes in patients with acute myeloid leukemia
title Assessment of the presence and anti-tumor potential of tumor-infiltrating lymphocytes in patients with acute myeloid leukemia
title_full Assessment of the presence and anti-tumor potential of tumor-infiltrating lymphocytes in patients with acute myeloid leukemia
title_fullStr Assessment of the presence and anti-tumor potential of tumor-infiltrating lymphocytes in patients with acute myeloid leukemia
title_full_unstemmed Assessment of the presence and anti-tumor potential of tumor-infiltrating lymphocytes in patients with acute myeloid leukemia
title_short Assessment of the presence and anti-tumor potential of tumor-infiltrating lymphocytes in patients with acute myeloid leukemia
title_sort assessment of the presence and anti-tumor potential of tumor-infiltrating lymphocytes in patients with acute myeloid leukemia
topic Original Research
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6489577/
https://www.ncbi.nlm.nih.gov/pubmed/31114360
http://dx.doi.org/10.2147/CMAR.S199817
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