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Radiotherapy enhances CXCR3(high)CD8(+) T cell activation through inducing IFNγ-mediated CXCL10 and ICAM-1 expression in lung cancer cells
Radiotherapy (RT) not only damages tumors but also induces interferon (IFN) expression in tumors. IFNs mediate PD-L1 to exhaust CD8(+) T cells, but which also directly impact tumor cells and potentially activate anti-tumor immune surveillance. Little is known about the contradictory mechanism of IFN...
Autores principales: | , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Springer Berlin Heidelberg
2023
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10198930/ https://www.ncbi.nlm.nih.gov/pubmed/36688994 http://dx.doi.org/10.1007/s00262-023-03379-6 |
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author | Wang, Chih-Liang Ho, Ai-Sheng Chang, Chun-Chao Sie, Zong-Lin Peng, Cheng-Liang Chang, Jungshan Cheng, Chun-Chia |
author_facet | Wang, Chih-Liang Ho, Ai-Sheng Chang, Chun-Chao Sie, Zong-Lin Peng, Cheng-Liang Chang, Jungshan Cheng, Chun-Chia |
author_sort | Wang, Chih-Liang |
collection | PubMed |
description | Radiotherapy (RT) not only damages tumors but also induces interferon (IFN) expression in tumors. IFNs mediate PD-L1 to exhaust CD8(+) T cells, but which also directly impact tumor cells and potentially activate anti-tumor immune surveillance. Little is known about the contradictory mechanism of IFNs in regulating CD8(+) T-mediated anti-tumor activity in lung cancer. This study found that RT induced IFNs and CXCL9/10 expression in the RT-treated lung cancer cells. Specifically, RT- and IFNγ-pretreated A549 significantly activated CD8(+) T cells, resulting in significant inhibition of A549 colony formation. RNAseq and consequent qPCR results revealed that IFNγ induced PD-L1, CXCL10, and ICAM-1, whereas PD-L1 knockdown activated CD8(+) T cells, but ICAM-1 knockdown diminished CD8(+) T cell activation. We further demonstrated that CXCR3 and CXCL10 decreased in the CD8(+) T cells and nonCD8(+) PBMCs, respectively, in the patients with lung cancer that expressed lower reactivation as co-cultured with A549 cells. In addition, inhibitors targeting CXCR3 and LFA-1 in CD8(+) T cells significantly diminished CD8(+) T cell activation and splenocytes-mediated anti-LL/2shPdl1. In conclusion, we validated that RT suppressed lung cancer and overexpress PD-L1, CXCL10, and ICAM-1, which exhibited different roles in regulating CD8(+) T cell activity. We propose that CXCR3(high)CD8(+) T cells stimulated by CXCL10 exhibit anti-tumor immunity, possibly by enhancing T cells-tumor cells adhesion through CXCL10/CXCR3-activated LFA-1-ICAM-1 interaction, but CXCR3(low)CD8(+) T cells with low CXCL10 in patients with lung cancer were exhausted by PD-L1 dominantly. Therefore, RT potentially activates CD8(+) T cells by inducing IFNs-mediated CXCL10 and ICAM-1 expression in tumors to enhance CD8(+) T-tumor adhesion and recognition. This study clarified the possible mechanisms of RT and IFNs in regulating CD8(+) T cell activation in lung cancer. SUPPLEMENTARY INFORMATION: The online version contains supplementary material available at 10.1007/s00262-023-03379-6. |
format | Online Article Text |
id | pubmed-10198930 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2023 |
publisher | Springer Berlin Heidelberg |
record_format | MEDLINE/PubMed |
spelling | pubmed-101989302023-05-21 Radiotherapy enhances CXCR3(high)CD8(+) T cell activation through inducing IFNγ-mediated CXCL10 and ICAM-1 expression in lung cancer cells Wang, Chih-Liang Ho, Ai-Sheng Chang, Chun-Chao Sie, Zong-Lin Peng, Cheng-Liang Chang, Jungshan Cheng, Chun-Chia Cancer Immunol Immunother Research Radiotherapy (RT) not only damages tumors but also induces interferon (IFN) expression in tumors. IFNs mediate PD-L1 to exhaust CD8(+) T cells, but which also directly impact tumor cells and potentially activate anti-tumor immune surveillance. Little is known about the contradictory mechanism of IFNs in regulating CD8(+) T-mediated anti-tumor activity in lung cancer. This study found that RT induced IFNs and CXCL9/10 expression in the RT-treated lung cancer cells. Specifically, RT- and IFNγ-pretreated A549 significantly activated CD8(+) T cells, resulting in significant inhibition of A549 colony formation. RNAseq and consequent qPCR results revealed that IFNγ induced PD-L1, CXCL10, and ICAM-1, whereas PD-L1 knockdown activated CD8(+) T cells, but ICAM-1 knockdown diminished CD8(+) T cell activation. We further demonstrated that CXCR3 and CXCL10 decreased in the CD8(+) T cells and nonCD8(+) PBMCs, respectively, in the patients with lung cancer that expressed lower reactivation as co-cultured with A549 cells. In addition, inhibitors targeting CXCR3 and LFA-1 in CD8(+) T cells significantly diminished CD8(+) T cell activation and splenocytes-mediated anti-LL/2shPdl1. In conclusion, we validated that RT suppressed lung cancer and overexpress PD-L1, CXCL10, and ICAM-1, which exhibited different roles in regulating CD8(+) T cell activity. We propose that CXCR3(high)CD8(+) T cells stimulated by CXCL10 exhibit anti-tumor immunity, possibly by enhancing T cells-tumor cells adhesion through CXCL10/CXCR3-activated LFA-1-ICAM-1 interaction, but CXCR3(low)CD8(+) T cells with low CXCL10 in patients with lung cancer were exhausted by PD-L1 dominantly. Therefore, RT potentially activates CD8(+) T cells by inducing IFNs-mediated CXCL10 and ICAM-1 expression in tumors to enhance CD8(+) T-tumor adhesion and recognition. This study clarified the possible mechanisms of RT and IFNs in regulating CD8(+) T cell activation in lung cancer. SUPPLEMENTARY INFORMATION: The online version contains supplementary material available at 10.1007/s00262-023-03379-6. Springer Berlin Heidelberg 2023-01-23 2023 /pmc/articles/PMC10198930/ /pubmed/36688994 http://dx.doi.org/10.1007/s00262-023-03379-6 Text en © The Author(s) 2023 https://creativecommons.org/licenses/by/4.0/Open AccessThis article is licensed under a Creative Commons Attribution 4.0 International License, which permits use, sharing, adaptation, distribution and reproduction in any medium or format, as long as you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons licence, and indicate if changes were made. The images or other third party material in this article are included in the article's Creative Commons licence, unless indicated otherwise in a credit line to the material. If material is not included in the article's Creative Commons licence and your intended use is not permitted by statutory regulation or exceeds the permitted use, you will need to obtain permission directly from the copyright holder. To view a copy of this licence, visit http://creativecommons.org/licenses/by/4.0/ (https://creativecommons.org/licenses/by/4.0/) . |
spellingShingle | Research Wang, Chih-Liang Ho, Ai-Sheng Chang, Chun-Chao Sie, Zong-Lin Peng, Cheng-Liang Chang, Jungshan Cheng, Chun-Chia Radiotherapy enhances CXCR3(high)CD8(+) T cell activation through inducing IFNγ-mediated CXCL10 and ICAM-1 expression in lung cancer cells |
title | Radiotherapy enhances CXCR3(high)CD8(+) T cell activation through inducing IFNγ-mediated CXCL10 and ICAM-1 expression in lung cancer cells |
title_full | Radiotherapy enhances CXCR3(high)CD8(+) T cell activation through inducing IFNγ-mediated CXCL10 and ICAM-1 expression in lung cancer cells |
title_fullStr | Radiotherapy enhances CXCR3(high)CD8(+) T cell activation through inducing IFNγ-mediated CXCL10 and ICAM-1 expression in lung cancer cells |
title_full_unstemmed | Radiotherapy enhances CXCR3(high)CD8(+) T cell activation through inducing IFNγ-mediated CXCL10 and ICAM-1 expression in lung cancer cells |
title_short | Radiotherapy enhances CXCR3(high)CD8(+) T cell activation through inducing IFNγ-mediated CXCL10 and ICAM-1 expression in lung cancer cells |
title_sort | radiotherapy enhances cxcr3(high)cd8(+) t cell activation through inducing ifnγ-mediated cxcl10 and icam-1 expression in lung cancer cells |
topic | Research |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10198930/ https://www.ncbi.nlm.nih.gov/pubmed/36688994 http://dx.doi.org/10.1007/s00262-023-03379-6 |
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