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The safety and anti-tumor effect of multiple peptides-pulsed dendritic cells combined with induced specific cytotoxic T lymphocytes for patients with solid tumors

OBJECTIVE: The aim of this study was to explore the safety and efficacy of multiple peptide-pulsed autologous dendritic cells (DCs) combined with cytotoxic T lymphocytes (CTLs) in patients with cancer. METHODS: Five patients diagnosed with cancer between November 2020 and June 2021 were enrolled and...

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Autores principales: Zhao, Xuan, Zhang, Zhen, Wen, Chunli, Huang, Jianmin, Yang, Shuangning, Liu, Jinyan, Geng, Huizhen, Peng, Bing, Li, Zibo, Zhang, Yi
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Frontiers Media S.A. 2023
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10628471/
https://www.ncbi.nlm.nih.gov/pubmed/37942324
http://dx.doi.org/10.3389/fimmu.2023.1284334
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author Zhao, Xuan
Zhang, Zhen
Wen, Chunli
Huang, Jianmin
Yang, Shuangning
Liu, Jinyan
Geng, Huizhen
Peng, Bing
Li, Zibo
Zhang, Yi
author_facet Zhao, Xuan
Zhang, Zhen
Wen, Chunli
Huang, Jianmin
Yang, Shuangning
Liu, Jinyan
Geng, Huizhen
Peng, Bing
Li, Zibo
Zhang, Yi
author_sort Zhao, Xuan
collection PubMed
description OBJECTIVE: The aim of this study was to explore the safety and efficacy of multiple peptide-pulsed autologous dendritic cells (DCs) combined with cytotoxic T lymphocytes (CTLs) in patients with cancer. METHODS: Five patients diagnosed with cancer between November 2020 and June 2021 were enrolled and received DC-CTLs therapy. Peripheral blood was collected and antigenic peptides were analyzed. The phenotype and function of DC-CTLs and the immune status of patients were detected using flow cytometry or IFN-γ ELISPOT analysis. RESULTS: DCs acquired a mature phenotype and expressed high levels of CD80, CD86, CD83, and HLA-DR after co-culture with peptides, and the DC-CTLs also exhibited high levels of IFN-γ. Peripheral blood mononuclear cells from post-treatment patients showed a stronger immune response to peptides than those prior to treatment. Importantly, four of five patients maintained a favorable immune status, of which one patient’s disease-free survival lasted up to 28.2 months. No severe treatment-related adverse events were observed. CONCLUSION: Our results show that multiple peptide-pulsed DCs combined with CTLs therapy has manageable safety and promising efficacy for cancer patients, which might provide a precise immunotherapeutic strategy for cancer.
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spelling pubmed-106284712023-11-08 The safety and anti-tumor effect of multiple peptides-pulsed dendritic cells combined with induced specific cytotoxic T lymphocytes for patients with solid tumors Zhao, Xuan Zhang, Zhen Wen, Chunli Huang, Jianmin Yang, Shuangning Liu, Jinyan Geng, Huizhen Peng, Bing Li, Zibo Zhang, Yi Front Immunol Immunology OBJECTIVE: The aim of this study was to explore the safety and efficacy of multiple peptide-pulsed autologous dendritic cells (DCs) combined with cytotoxic T lymphocytes (CTLs) in patients with cancer. METHODS: Five patients diagnosed with cancer between November 2020 and June 2021 were enrolled and received DC-CTLs therapy. Peripheral blood was collected and antigenic peptides were analyzed. The phenotype and function of DC-CTLs and the immune status of patients were detected using flow cytometry or IFN-γ ELISPOT analysis. RESULTS: DCs acquired a mature phenotype and expressed high levels of CD80, CD86, CD83, and HLA-DR after co-culture with peptides, and the DC-CTLs also exhibited high levels of IFN-γ. Peripheral blood mononuclear cells from post-treatment patients showed a stronger immune response to peptides than those prior to treatment. Importantly, four of five patients maintained a favorable immune status, of which one patient’s disease-free survival lasted up to 28.2 months. No severe treatment-related adverse events were observed. CONCLUSION: Our results show that multiple peptide-pulsed DCs combined with CTLs therapy has manageable safety and promising efficacy for cancer patients, which might provide a precise immunotherapeutic strategy for cancer. Frontiers Media S.A. 2023-10-24 /pmc/articles/PMC10628471/ /pubmed/37942324 http://dx.doi.org/10.3389/fimmu.2023.1284334 Text en Copyright © 2023 Zhao, Zhang, Wen, Huang, Yang, Liu, Geng, Peng, Li and Zhang 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
Zhao, Xuan
Zhang, Zhen
Wen, Chunli
Huang, Jianmin
Yang, Shuangning
Liu, Jinyan
Geng, Huizhen
Peng, Bing
Li, Zibo
Zhang, Yi
The safety and anti-tumor effect of multiple peptides-pulsed dendritic cells combined with induced specific cytotoxic T lymphocytes for patients with solid tumors
title The safety and anti-tumor effect of multiple peptides-pulsed dendritic cells combined with induced specific cytotoxic T lymphocytes for patients with solid tumors
title_full The safety and anti-tumor effect of multiple peptides-pulsed dendritic cells combined with induced specific cytotoxic T lymphocytes for patients with solid tumors
title_fullStr The safety and anti-tumor effect of multiple peptides-pulsed dendritic cells combined with induced specific cytotoxic T lymphocytes for patients with solid tumors
title_full_unstemmed The safety and anti-tumor effect of multiple peptides-pulsed dendritic cells combined with induced specific cytotoxic T lymphocytes for patients with solid tumors
title_short The safety and anti-tumor effect of multiple peptides-pulsed dendritic cells combined with induced specific cytotoxic T lymphocytes for patients with solid tumors
title_sort safety and anti-tumor effect of multiple peptides-pulsed dendritic cells combined with induced specific cytotoxic t lymphocytes for patients with solid tumors
topic Immunology
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10628471/
https://www.ncbi.nlm.nih.gov/pubmed/37942324
http://dx.doi.org/10.3389/fimmu.2023.1284334
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