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CD8+ T cell response to human papillomavirus 16 E7 is able to predict survival outcome in oropharyngeal cancer

CD8+ T cell response to human papillomavirus 16 E7 is able to predict survival outcome in oropharyngeal cancer
CD8+ T cell response to human papillomavirus 16 E7 is able to predict survival outcome in oropharyngeal cancer
Introduction: Immunological response to human papillomavirus (HPV) in the development and progression of HPV16+ oropharyngeal squamous cell carcinoma (OPSCC) (accounting for the majority of viral associated cases) is largely unknown and may provide important insights for new therapeutic strategies. Methods: In this prospective clinical trial (UKCRN11945), we examined cell-mediated immune responses to HPV16 E2, E6 and E7 in peripheral blood using IFN-gamma enzyme-linked immunosorbent spot assay. CD56+, CD4+, CD8+ and regulatory T cell frequencies were also discerned by flow cytometry. Fifty-one study participants with oropharyngeal carcinoma were recruited. Control subjects were those undergoing tonsillectomy for benign disease. All patients were treated with curative intent by radiotherapy $ chemotherapy. Disease-specific survival was investigated by multivariate analysis. Results: HPV16 DNA was detected in 41/51 of the OPSCC participants. T cell responses against HPV16 E6 or E7 peptides were detected in 33/51 evaluable patients, respectively and correlated with HPV status. Matched pre- and post-treatment T cell responses were available for 39/51 OPSCC cases. Within the whole cohort, elevated post-treatment CD8+ response to HPV16 E7 correlated with longer disease free survival (multivariate DFS p <0.03). Within the HPV + OPSCC cohort, a significant increase in regulatory T cells (p <0.02) was noted after treatment. Conclusions: This is the first study to provide survival data in OPSCC stratified by cell-mediated immune response to HPV16 peptides. Within the HPV16+ OPSCC cohort, enhanced immunoreactivity to antigen E7 was linked to improved survival. An increase in regulatory T cell frequencies after treatment may suggest that immunosuppression can contribute to a reduced HPV-specific cell-mediated response.
Human papillomavirus, Oropharyngeal carcinoma, Cell-mediated immunity, Interferon-?, School of Biosciences
0959-8049
141-151
Masterson, L
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Lechner, M
19c72359-7dc0-435c-817a-f67d4956656f
Loewenbein, S
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Mohammed, H
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Davies-Husband, C
cf01b428-7ec1-4218-894e-bdb8f7162579
Fenton, TR
087260ba-f6a1-405a-85df-099d05810a84
Sudhoff, H
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Jani, P
cdbebb01-7572-4455-b7f6-2a4159f321ae
Goon, P
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Sterling, J
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Masterson, L
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Lechner, M
19c72359-7dc0-435c-817a-f67d4956656f
Loewenbein, S
b614e101-bd19-4bdd-a2f4-03c6c815cee8
Mohammed, H
e3894802-1b10-4e51-9f65-cbff9d7fbf70
Davies-Husband, C
cf01b428-7ec1-4218-894e-bdb8f7162579
Fenton, TR
087260ba-f6a1-405a-85df-099d05810a84
Sudhoff, H
76eb0dbd-a3b6-4d09-95c7-cca5c7ab7499
Jani, P
cdbebb01-7572-4455-b7f6-2a4159f321ae
Goon, P
0490cd4d-2ce4-433a-a56c-06398e461e00
Sterling, J
86052bc8-c877-47cc-a21d-5dff7a5dd526

Masterson, L, Lechner, M, Loewenbein, S, Mohammed, H, Davies-Husband, C, Fenton, TR, Sudhoff, H, Jani, P, Goon, P and Sterling, J (2016) CD8+ T cell response to human papillomavirus 16 E7 is able to predict survival outcome in oropharyngeal cancer. European Journal of Cancer, 67 (C), 141-151. (doi:10.1016/j.ejca.2016.08.012).

Record type: Article

Abstract

Introduction: Immunological response to human papillomavirus (HPV) in the development and progression of HPV16+ oropharyngeal squamous cell carcinoma (OPSCC) (accounting for the majority of viral associated cases) is largely unknown and may provide important insights for new therapeutic strategies. Methods: In this prospective clinical trial (UKCRN11945), we examined cell-mediated immune responses to HPV16 E2, E6 and E7 in peripheral blood using IFN-gamma enzyme-linked immunosorbent spot assay. CD56+, CD4+, CD8+ and regulatory T cell frequencies were also discerned by flow cytometry. Fifty-one study participants with oropharyngeal carcinoma were recruited. Control subjects were those undergoing tonsillectomy for benign disease. All patients were treated with curative intent by radiotherapy $ chemotherapy. Disease-specific survival was investigated by multivariate analysis. Results: HPV16 DNA was detected in 41/51 of the OPSCC participants. T cell responses against HPV16 E6 or E7 peptides were detected in 33/51 evaluable patients, respectively and correlated with HPV status. Matched pre- and post-treatment T cell responses were available for 39/51 OPSCC cases. Within the whole cohort, elevated post-treatment CD8+ response to HPV16 E7 correlated with longer disease free survival (multivariate DFS p <0.03). Within the HPV + OPSCC cohort, a significant increase in regulatory T cells (p <0.02) was noted after treatment. Conclusions: This is the first study to provide survival data in OPSCC stratified by cell-mediated immune response to HPV16 peptides. Within the HPV16+ OPSCC cohort, enhanced immunoreactivity to antigen E7 was linked to improved survival. An increase in regulatory T cell frequencies after treatment may suggest that immunosuppression can contribute to a reduced HPV-specific cell-mediated response.

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More information

e-pub ahead of print date: 1 September 2016
Published date: November 2016
Additional Information: publisher: Elsevier articletitle: CD8+ T cell response to human papillomavirus 16 E7 is able to predict survival outcome in oropharyngeal cancer journaltitle: European Journal of Cancer articlelink: http://dx.doi.org/10.1016/j.ejca.2016.08.012 contenttype: article copyright: copyright 2016 Elsevier Ltd. All rights reserved.
Keywords: Human papillomavirus, Oropharyngeal carcinoma, Cell-mediated immunity, Interferon-?, School of Biosciences

Identifiers

Local EPrints ID: 453901
URI: http://eprints.soton.ac.uk/id/eprint/453901
ISSN: 0959-8049
PURE UUID: 1f7396a7-5d5c-4332-9410-4dacc3198ad8
ORCID for TR Fenton: ORCID iD orcid.org/0000-0002-4737-8233

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Date deposited: 25 Jan 2022 17:50
Last modified: 17 Mar 2024 04:11

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Contributors

Author: L Masterson
Author: M Lechner
Author: S Loewenbein
Author: H Mohammed
Author: C Davies-Husband
Author: TR Fenton ORCID iD
Author: H Sudhoff
Author: P Jani
Author: P Goon
Author: J Sterling

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