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Immune responses against autologous tumor and human papilloma virus in lymph nodes from patients with penile cancer
PURPOSE: Nearly half of penile cancers are related to human papillomavirus (HPV) infection. Investigations of tumor- and HPV-specific T cell reactivity in regional lymph nodes (LNs) from patients with penile cancer are warranted. MATERIALS AND METHODS: In this study, single-cell suspensions from LNs...
Autores principales: | , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
The Korean Urological Association
2021
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7801168/ https://www.ncbi.nlm.nih.gov/pubmed/33314806 http://dx.doi.org/10.4111/icu.20200116 |
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author | Zhang, Lu Zirakzadeh, A. Ali Rosvall, Jesper Hedlund, Mats Hu, Ping Sheng Riklund, Katrine Sherif, Amir Winqvist, Ola |
author_facet | Zhang, Lu Zirakzadeh, A. Ali Rosvall, Jesper Hedlund, Mats Hu, Ping Sheng Riklund, Katrine Sherif, Amir Winqvist, Ola |
author_sort | Zhang, Lu |
collection | PubMed |
description | PURPOSE: Nearly half of penile cancers are related to human papillomavirus (HPV) infection. Investigations of tumor- and HPV-specific T cell reactivity in regional lymph nodes (LNs) from patients with penile cancer are warranted. MATERIALS AND METHODS: In this study, single-cell suspensions from LNs and peripheral blood from 11 patients with penile cancer were stained with antibodies for lymphocyte markers and analyzed by fluorescence-activated cell sorting (FACS). DNA was extracted from the tumor tissue and HPV status was investigated by PCR. RESULTS: T-cell reactivity against autologous tumor-extract and against the HPV-vaccine Gardasil® was tested by flow-cytometric assay of specific cell-mediated immune response in activated whole blood (FASCIA). CD4(+)/CD8(+) ratios were significantly lower in HPV positive LNs (p<0.05). Immune responses to tumor extract assessed by blast transformation and expansion in vitro, of either CD4(+) or CD8(+) T-cells, were found in 9 of 13 LNs (69%). 5 of 6 tested patients demonstrated T cell recognition of tumor-associated antigen(s). In HPV-positive patients, dose-dependent T cell responses against L1 (late) HPV proteins (Gardasil vaccine) were demonstrated. CONCLUSIONS: LN-derived T cells from patients with penile cancer recognize tumor antigen(s) and in HPV-positive cases, there is a response against L1 (late) HPV proteins, being constituents of the Gardasil vaccine. |
format | Online Article Text |
id | pubmed-7801168 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2021 |
publisher | The Korean Urological Association |
record_format | MEDLINE/PubMed |
spelling | pubmed-78011682021-01-21 Immune responses against autologous tumor and human papilloma virus in lymph nodes from patients with penile cancer Zhang, Lu Zirakzadeh, A. Ali Rosvall, Jesper Hedlund, Mats Hu, Ping Sheng Riklund, Katrine Sherif, Amir Winqvist, Ola Investig Clin Urol Original Article PURPOSE: Nearly half of penile cancers are related to human papillomavirus (HPV) infection. Investigations of tumor- and HPV-specific T cell reactivity in regional lymph nodes (LNs) from patients with penile cancer are warranted. MATERIALS AND METHODS: In this study, single-cell suspensions from LNs and peripheral blood from 11 patients with penile cancer were stained with antibodies for lymphocyte markers and analyzed by fluorescence-activated cell sorting (FACS). DNA was extracted from the tumor tissue and HPV status was investigated by PCR. RESULTS: T-cell reactivity against autologous tumor-extract and against the HPV-vaccine Gardasil® was tested by flow-cytometric assay of specific cell-mediated immune response in activated whole blood (FASCIA). CD4(+)/CD8(+) ratios were significantly lower in HPV positive LNs (p<0.05). Immune responses to tumor extract assessed by blast transformation and expansion in vitro, of either CD4(+) or CD8(+) T-cells, were found in 9 of 13 LNs (69%). 5 of 6 tested patients demonstrated T cell recognition of tumor-associated antigen(s). In HPV-positive patients, dose-dependent T cell responses against L1 (late) HPV proteins (Gardasil vaccine) were demonstrated. CONCLUSIONS: LN-derived T cells from patients with penile cancer recognize tumor antigen(s) and in HPV-positive cases, there is a response against L1 (late) HPV proteins, being constituents of the Gardasil vaccine. The Korean Urological Association 2021-01 2020-12-10 /pmc/articles/PMC7801168/ /pubmed/33314806 http://dx.doi.org/10.4111/icu.20200116 Text en © The Korean Urological Association, 2021 http://creativecommons.org/licenses/by-nc/4.0 This is an Open Access article distributed under the terms of the Creative Commons Attribution Non-Commercial License (http://creativecommons.org/licenses/by-nc/4.0) which permits unrestricted non-commercial use, distribution, and reproduction in any medium, provided the original work is properly cited. |
spellingShingle | Original Article Zhang, Lu Zirakzadeh, A. Ali Rosvall, Jesper Hedlund, Mats Hu, Ping Sheng Riklund, Katrine Sherif, Amir Winqvist, Ola Immune responses against autologous tumor and human papilloma virus in lymph nodes from patients with penile cancer |
title | Immune responses against autologous tumor and human papilloma virus in lymph nodes from patients with penile cancer |
title_full | Immune responses against autologous tumor and human papilloma virus in lymph nodes from patients with penile cancer |
title_fullStr | Immune responses against autologous tumor and human papilloma virus in lymph nodes from patients with penile cancer |
title_full_unstemmed | Immune responses against autologous tumor and human papilloma virus in lymph nodes from patients with penile cancer |
title_short | Immune responses against autologous tumor and human papilloma virus in lymph nodes from patients with penile cancer |
title_sort | immune responses against autologous tumor and human papilloma virus in lymph nodes from patients with penile cancer |
topic | Original Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7801168/ https://www.ncbi.nlm.nih.gov/pubmed/33314806 http://dx.doi.org/10.4111/icu.20200116 |
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