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Profiling HPV-16–specific T cell responses reveals broad antigen reactivities in oropharyngeal cancer patients
Cellular immunotherapeutics targeting the human papillomavirus (HPV)–16 E6 and E7 proteins have achieved limited success in HPV-positive oropharyngeal cancer (OPC). Here we have conducted proteome-wide profiling of HPV-16–specific T cell responses in a cohort of 66 patients with HPV-associated OPC a...
Autores principales: | , , , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Rockefeller University Press
2020
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7537390/ https://www.ncbi.nlm.nih.gov/pubmed/32716518 http://dx.doi.org/10.1084/jem.20200389 |
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author | Bhatt, Kunal H. Neller, Michelle A. Srihari, Sriganesh Crooks, Pauline Lekieffre, Lea Aftab, Blake T. Liu, Howard Smith, Corey Kenny, Liz Porceddu, Sandro Khanna, Rajiv |
author_facet | Bhatt, Kunal H. Neller, Michelle A. Srihari, Sriganesh Crooks, Pauline Lekieffre, Lea Aftab, Blake T. Liu, Howard Smith, Corey Kenny, Liz Porceddu, Sandro Khanna, Rajiv |
author_sort | Bhatt, Kunal H. |
collection | PubMed |
description | Cellular immunotherapeutics targeting the human papillomavirus (HPV)–16 E6 and E7 proteins have achieved limited success in HPV-positive oropharyngeal cancer (OPC). Here we have conducted proteome-wide profiling of HPV-16–specific T cell responses in a cohort of 66 patients with HPV-associated OPC and 22 healthy individuals. Unexpectedly, HPV-specific T cell responses from OPC patients were not constrained to the E6 and E7 antigens; they also recognized E1, E2, E4, E5, and L1 proteins as dominant targets for virus-specific CD8(+) and CD4(+) T cells. Multivariate analysis incorporating tumor staging, treatment status, and smoking history revealed that treatment status had the most significant impact on HPV-specific CD8(+) and CD4(+) T cell immunity. Specifically, the breadth and overall strength of HPV-specific T cell responses were significantly higher before the commencement of curative therapy than after therapy. These data provide the first glimpse of the overall human T cell response to HPV in a clinical setting and offer groundbreaking insight into future development of cellular immunotherapies for HPV-associated OPC patients. |
format | Online Article Text |
id | pubmed-7537390 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2020 |
publisher | Rockefeller University Press |
record_format | MEDLINE/PubMed |
spelling | pubmed-75373902021-04-05 Profiling HPV-16–specific T cell responses reveals broad antigen reactivities in oropharyngeal cancer patients Bhatt, Kunal H. Neller, Michelle A. Srihari, Sriganesh Crooks, Pauline Lekieffre, Lea Aftab, Blake T. Liu, Howard Smith, Corey Kenny, Liz Porceddu, Sandro Khanna, Rajiv J Exp Med Article Cellular immunotherapeutics targeting the human papillomavirus (HPV)–16 E6 and E7 proteins have achieved limited success in HPV-positive oropharyngeal cancer (OPC). Here we have conducted proteome-wide profiling of HPV-16–specific T cell responses in a cohort of 66 patients with HPV-associated OPC and 22 healthy individuals. Unexpectedly, HPV-specific T cell responses from OPC patients were not constrained to the E6 and E7 antigens; they also recognized E1, E2, E4, E5, and L1 proteins as dominant targets for virus-specific CD8(+) and CD4(+) T cells. Multivariate analysis incorporating tumor staging, treatment status, and smoking history revealed that treatment status had the most significant impact on HPV-specific CD8(+) and CD4(+) T cell immunity. Specifically, the breadth and overall strength of HPV-specific T cell responses were significantly higher before the commencement of curative therapy than after therapy. These data provide the first glimpse of the overall human T cell response to HPV in a clinical setting and offer groundbreaking insight into future development of cellular immunotherapies for HPV-associated OPC patients. Rockefeller University Press 2020-07-27 /pmc/articles/PMC7537390/ /pubmed/32716518 http://dx.doi.org/10.1084/jem.20200389 Text en © 2020 Bhatt et al. http://www.rupress.org/terms/https://creativecommons.org/licenses/by-nc-sa/4.0/This article is distributed under the terms of an Attribution–Noncommercial–Share Alike–No Mirror Sites license for the first six months after the publication date (see http://www.rupress.org/terms/). After six months it is available under a Creative Commons License (Attribution–Noncommercial–Share Alike 4.0 International license, as described at https://creativecommons.org/licenses/by-nc-sa/4.0/). |
spellingShingle | Article Bhatt, Kunal H. Neller, Michelle A. Srihari, Sriganesh Crooks, Pauline Lekieffre, Lea Aftab, Blake T. Liu, Howard Smith, Corey Kenny, Liz Porceddu, Sandro Khanna, Rajiv Profiling HPV-16–specific T cell responses reveals broad antigen reactivities in oropharyngeal cancer patients |
title | Profiling HPV-16–specific T cell responses reveals broad antigen reactivities in oropharyngeal cancer patients |
title_full | Profiling HPV-16–specific T cell responses reveals broad antigen reactivities in oropharyngeal cancer patients |
title_fullStr | Profiling HPV-16–specific T cell responses reveals broad antigen reactivities in oropharyngeal cancer patients |
title_full_unstemmed | Profiling HPV-16–specific T cell responses reveals broad antigen reactivities in oropharyngeal cancer patients |
title_short | Profiling HPV-16–specific T cell responses reveals broad antigen reactivities in oropharyngeal cancer patients |
title_sort | profiling hpv-16–specific t cell responses reveals broad antigen reactivities in oropharyngeal cancer patients |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7537390/ https://www.ncbi.nlm.nih.gov/pubmed/32716518 http://dx.doi.org/10.1084/jem.20200389 |
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