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Antigen-specific CD8+ memory stem T cells generated from human peripheral blood effectively eradicate allogeneic targets in mice
BACKGROUND: As the implantation and long-term existence of tumor-specific T cells in host are the prerequisite for adoptive immunotherapy, memory stem T cells (T(SCM)) with self-renewal and differentiation capacity show the greatest potential to implant and long-term exhibit function in vivo, compar...
Autores principales: | , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
BioMed Central
2018
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6286512/ https://www.ncbi.nlm.nih.gov/pubmed/30526661 http://dx.doi.org/10.1186/s13287-018-1080-1 |
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author | Guan, Liping Li, Xiaoyi Wei, Jiali Liang, Zhihui Yang, Jing Weng, Xiufang Wu, Xiongwen |
author_facet | Guan, Liping Li, Xiaoyi Wei, Jiali Liang, Zhihui Yang, Jing Weng, Xiufang Wu, Xiongwen |
author_sort | Guan, Liping |
collection | PubMed |
description | BACKGROUND: As the implantation and long-term existence of tumor-specific T cells in host are the prerequisite for adoptive immunotherapy, memory stem T cells (T(SCM)) with self-renewal and differentiation capacity show the greatest potential to implant and long-term exhibit function in vivo, compared with other T cells of differentiation stages. Hence, tumor-specific T(SCM) have become potential candidate for adoptive T cell therapy of cancer. Here, we reported a protocol to generate allogeneic antigen-specific CD8+ T(SCM) cells from human PBLs. METHODS: To prepare allogeneic antigen-specific CD8+ T(SCM), we used an LCL named E007 of defined HLA allotyping as simulator, a co-culture of E007 and allogeneic PBLs was carried out in the presence of differentiation inhibitor TWS119 for 7 days. Sorting of proliferation cells ensured the E007-specificity of the prepared T(SCM) cells. The sorted lymphocytes underwent further expansion by cytokines IL-7 and IL-15 for further 7 days, making the E007-specific CD8 + T(SCM) expanded in number. The stem cell and T memory cell properties of the prepared CD8+ T(SCM) were observed in NOD-SCID mice. RESULTS: Our protocol began with 1 × 10(7) PBLs and resulted in 2 × 10(7) E007-specific CD8+ T(SCM) cells in 2 weeks of preparation. The prepared T(SCM) cells exhibited a proliferative history and rapid differentiation into effector cells upon the E007 re-stimulation. Importantly, the prepared T(SCM) cells were able to exist long and reconstitute other T cell subsets in vivo, eradicating the E007 cells effectively after transferred into the LCL burden mice. CONCLUSIONS: This protocol was able to prepare allogeneic antigen-specific CD8+ T(SCM) cells from human PBLs. The prepared T(SCM) showed the properties of stem cells and T memory cells. This study provided a reference method for generation of antigen-specific T(SCM) for T cell adoptive immunotherapy. ELECTRONIC SUPPLEMENTARY MATERIAL: The online version of this article (10.1186/s13287-018-1080-1) contains supplementary material, which is available to authorized users. |
format | Online Article Text |
id | pubmed-6286512 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2018 |
publisher | BioMed Central |
record_format | MEDLINE/PubMed |
spelling | pubmed-62865122018-12-14 Antigen-specific CD8+ memory stem T cells generated from human peripheral blood effectively eradicate allogeneic targets in mice Guan, Liping Li, Xiaoyi Wei, Jiali Liang, Zhihui Yang, Jing Weng, Xiufang Wu, Xiongwen Stem Cell Res Ther Research BACKGROUND: As the implantation and long-term existence of tumor-specific T cells in host are the prerequisite for adoptive immunotherapy, memory stem T cells (T(SCM)) with self-renewal and differentiation capacity show the greatest potential to implant and long-term exhibit function in vivo, compared with other T cells of differentiation stages. Hence, tumor-specific T(SCM) have become potential candidate for adoptive T cell therapy of cancer. Here, we reported a protocol to generate allogeneic antigen-specific CD8+ T(SCM) cells from human PBLs. METHODS: To prepare allogeneic antigen-specific CD8+ T(SCM), we used an LCL named E007 of defined HLA allotyping as simulator, a co-culture of E007 and allogeneic PBLs was carried out in the presence of differentiation inhibitor TWS119 for 7 days. Sorting of proliferation cells ensured the E007-specificity of the prepared T(SCM) cells. The sorted lymphocytes underwent further expansion by cytokines IL-7 and IL-15 for further 7 days, making the E007-specific CD8 + T(SCM) expanded in number. The stem cell and T memory cell properties of the prepared CD8+ T(SCM) were observed in NOD-SCID mice. RESULTS: Our protocol began with 1 × 10(7) PBLs and resulted in 2 × 10(7) E007-specific CD8+ T(SCM) cells in 2 weeks of preparation. The prepared T(SCM) cells exhibited a proliferative history and rapid differentiation into effector cells upon the E007 re-stimulation. Importantly, the prepared T(SCM) cells were able to exist long and reconstitute other T cell subsets in vivo, eradicating the E007 cells effectively after transferred into the LCL burden mice. CONCLUSIONS: This protocol was able to prepare allogeneic antigen-specific CD8+ T(SCM) cells from human PBLs. The prepared T(SCM) showed the properties of stem cells and T memory cells. This study provided a reference method for generation of antigen-specific T(SCM) for T cell adoptive immunotherapy. ELECTRONIC SUPPLEMENTARY MATERIAL: The online version of this article (10.1186/s13287-018-1080-1) contains supplementary material, which is available to authorized users. BioMed Central 2018-12-07 /pmc/articles/PMC6286512/ /pubmed/30526661 http://dx.doi.org/10.1186/s13287-018-1080-1 Text en © The Author(s). 2018 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 | Research Guan, Liping Li, Xiaoyi Wei, Jiali Liang, Zhihui Yang, Jing Weng, Xiufang Wu, Xiongwen Antigen-specific CD8+ memory stem T cells generated from human peripheral blood effectively eradicate allogeneic targets in mice |
title | Antigen-specific CD8+ memory stem T cells generated from human peripheral blood effectively eradicate allogeneic targets in mice |
title_full | Antigen-specific CD8+ memory stem T cells generated from human peripheral blood effectively eradicate allogeneic targets in mice |
title_fullStr | Antigen-specific CD8+ memory stem T cells generated from human peripheral blood effectively eradicate allogeneic targets in mice |
title_full_unstemmed | Antigen-specific CD8+ memory stem T cells generated from human peripheral blood effectively eradicate allogeneic targets in mice |
title_short | Antigen-specific CD8+ memory stem T cells generated from human peripheral blood effectively eradicate allogeneic targets in mice |
title_sort | antigen-specific cd8+ memory stem t cells generated from human peripheral blood effectively eradicate allogeneic targets in mice |
topic | Research |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6286512/ https://www.ncbi.nlm.nih.gov/pubmed/30526661 http://dx.doi.org/10.1186/s13287-018-1080-1 |
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