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Personal Neoantigens From Patients With NSCLC Induce Efficient Antitumor Responses

OBJECTIVE: To develop a neoantigen-targeted personalized cancer treatment for non-small cell lung cancer (NSCLC), neoantigens were obtained from collected human lung cancer samples, and the utility of neoantigen and neoantigen-reactive T cells (NRTs) was assessed. METHODS: Tumor specimens from three...

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Autores principales: Zhang, Wei, Yin, Qi, Huang, Haidong, Lu, Jingjing, Qin, Hao, Chen, Si, Zhang, Wenjun, Su, Xiaoping, Sun, Weihong, Dong, Yuchao, Li, Qiang
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Frontiers Media S.A. 2021
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8076796/
https://www.ncbi.nlm.nih.gov/pubmed/33928024
http://dx.doi.org/10.3389/fonc.2021.628456
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author Zhang, Wei
Yin, Qi
Huang, Haidong
Lu, Jingjing
Qin, Hao
Chen, Si
Zhang, Wenjun
Su, Xiaoping
Sun, Weihong
Dong, Yuchao
Li, Qiang
author_facet Zhang, Wei
Yin, Qi
Huang, Haidong
Lu, Jingjing
Qin, Hao
Chen, Si
Zhang, Wenjun
Su, Xiaoping
Sun, Weihong
Dong, Yuchao
Li, Qiang
author_sort Zhang, Wei
collection PubMed
description OBJECTIVE: To develop a neoantigen-targeted personalized cancer treatment for non-small cell lung cancer (NSCLC), neoantigens were obtained from collected human lung cancer samples, and the utility of neoantigen and neoantigen-reactive T cells (NRTs) was assessed. METHODS: Tumor specimens from three patients with NSCLC were obtained and analyzed by whole-exome sequencing, and neoantigens were predicted accordingly. Dendritic cells and T lymphocytes were isolated, NRTs were elicited and IFN-γ ELISPOT tests were conducted. HLA-A2.1/K(b) transgenic mice were immunized with peptides from HLA-A*02:01(+)patient with high immunogenicity, and NRTs were subjected to IFN-γ, IL-2 and TNF-α ELISPOT as well as time-resolved fluorescence assay for cytotoxicity assays to verify the immunogenicity in vitro. The HLA-A*02:01(+)lung cancer cell line was transfected with minigene and inoculated into the flanks of C57BL/6(nu/nu) mice and the NRTs induced by the immunogenic polypeptides from autologous HLA-A2.1/K(b) transgenic mice were adoptively transfused to verify their immunogenicity in vivo. RESULTS: Multiple putative mutation-associated neoantigens with strong affinity for HLA were selected from each patient. Immunogenic neoantigen were identified in all three NSCLC patients, the potency of ACAD8-T105I, BCAR1-G23V and PLCG1-M425L as effective neoantigen to active T cells in suppressing tumor growth was further proven both in vitro and in vivo using HLA-A2.1/Kb transgenic mice and tumor-bearing mouse models. CONCLUSION: Neoantigens with strong immunogenicity can be screened from NSCLC patients through the whole-exome sequencing of patient specimens and machine-learning-based neoantigen predictions. NRTs shown efficient antitumor responses in transgenic mice and tumor-bearing mouse models. Our results indicate that the development of neoantigen-based personalized immunotherapies in NSCLC is possible. PRECIS: Neoantigens with strong immunogenicity were screened from NSCLC patients. This research provides evidence suggesting that neoantigen-based therapy might serve as feasible treatment for NSCLC.
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spelling pubmed-80767962021-04-28 Personal Neoantigens From Patients With NSCLC Induce Efficient Antitumor Responses Zhang, Wei Yin, Qi Huang, Haidong Lu, Jingjing Qin, Hao Chen, Si Zhang, Wenjun Su, Xiaoping Sun, Weihong Dong, Yuchao Li, Qiang Front Oncol Oncology OBJECTIVE: To develop a neoantigen-targeted personalized cancer treatment for non-small cell lung cancer (NSCLC), neoantigens were obtained from collected human lung cancer samples, and the utility of neoantigen and neoantigen-reactive T cells (NRTs) was assessed. METHODS: Tumor specimens from three patients with NSCLC were obtained and analyzed by whole-exome sequencing, and neoantigens were predicted accordingly. Dendritic cells and T lymphocytes were isolated, NRTs were elicited and IFN-γ ELISPOT tests were conducted. HLA-A2.1/K(b) transgenic mice were immunized with peptides from HLA-A*02:01(+)patient with high immunogenicity, and NRTs were subjected to IFN-γ, IL-2 and TNF-α ELISPOT as well as time-resolved fluorescence assay for cytotoxicity assays to verify the immunogenicity in vitro. The HLA-A*02:01(+)lung cancer cell line was transfected with minigene and inoculated into the flanks of C57BL/6(nu/nu) mice and the NRTs induced by the immunogenic polypeptides from autologous HLA-A2.1/K(b) transgenic mice were adoptively transfused to verify their immunogenicity in vivo. RESULTS: Multiple putative mutation-associated neoantigens with strong affinity for HLA were selected from each patient. Immunogenic neoantigen were identified in all three NSCLC patients, the potency of ACAD8-T105I, BCAR1-G23V and PLCG1-M425L as effective neoantigen to active T cells in suppressing tumor growth was further proven both in vitro and in vivo using HLA-A2.1/Kb transgenic mice and tumor-bearing mouse models. CONCLUSION: Neoantigens with strong immunogenicity can be screened from NSCLC patients through the whole-exome sequencing of patient specimens and machine-learning-based neoantigen predictions. NRTs shown efficient antitumor responses in transgenic mice and tumor-bearing mouse models. Our results indicate that the development of neoantigen-based personalized immunotherapies in NSCLC is possible. PRECIS: Neoantigens with strong immunogenicity were screened from NSCLC patients. This research provides evidence suggesting that neoantigen-based therapy might serve as feasible treatment for NSCLC. Frontiers Media S.A. 2021-04-13 /pmc/articles/PMC8076796/ /pubmed/33928024 http://dx.doi.org/10.3389/fonc.2021.628456 Text en Copyright © 2021 Zhang, Yin, Huang, Lu, Qin, Chen, Zhang, Su, Sun, Dong and Li 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 Oncology
Zhang, Wei
Yin, Qi
Huang, Haidong
Lu, Jingjing
Qin, Hao
Chen, Si
Zhang, Wenjun
Su, Xiaoping
Sun, Weihong
Dong, Yuchao
Li, Qiang
Personal Neoantigens From Patients With NSCLC Induce Efficient Antitumor Responses
title Personal Neoantigens From Patients With NSCLC Induce Efficient Antitumor Responses
title_full Personal Neoantigens From Patients With NSCLC Induce Efficient Antitumor Responses
title_fullStr Personal Neoantigens From Patients With NSCLC Induce Efficient Antitumor Responses
title_full_unstemmed Personal Neoantigens From Patients With NSCLC Induce Efficient Antitumor Responses
title_short Personal Neoantigens From Patients With NSCLC Induce Efficient Antitumor Responses
title_sort personal neoantigens from patients with nsclc induce efficient antitumor responses
topic Oncology
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8076796/
https://www.ncbi.nlm.nih.gov/pubmed/33928024
http://dx.doi.org/10.3389/fonc.2021.628456
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