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dc.contributor.authorOguejiofor, Kenneth K
dc.contributor.authorGalletta-Williams, Henry
dc.contributor.authorDovedi, Simon J
dc.contributor.authorRoberts, Darren L
dc.contributor.authorStern, Peter L
dc.contributor.authorWest, Catharine M L
dc.date.accessioned2017-02-24T09:30:28Z
dc.date.available2017-02-24T09:30:28Z
dc.date.issued2017-01-22
dc.identifier.citationDistinct patterns of infiltrating CD8+ T cells in HPV+ and CD68 macrophages in HPV- oropharyngeal squamous cell carcinomas are associated with better clinical outcome but PD-L1 expression is not prognostic. 2017, Oncotargeten
dc.identifier.issn1949-2553
dc.identifier.pmid28122336
dc.identifier.doi10.18632/oncotarget.14796
dc.identifier.urihttp://hdl.handle.net/10541/620158
dc.description.abstractImmunotherapies are beginning to revolutionise treatment paradigms in oncology with monoclonal antibodies (mAb) targeting T-cell co-inhibitory (e.g. PD-1/PD-L1) and co-stimulatory pathways (e.g. CTLA-4/CD28) demonstrating clinical utility. Some clinical studies demonstrate that responsiveness to PD-1/PD-L1 mAb therapy is greater in patients with expression of PD-L1 in the tumour microenvironment. However, robust responses have also been observed in patients with low or absent expression of PD-L1. Using multiplex immuno-fluorescent labelling we sought to determine how infiltration of tumours by CD8+ T-cells, their expression of PD-1, and the expression of PD-L1 on both tumours and CD68 cells (macrophages) correlated with HPV status and outcome in a cohort of 124 oropharyngeal squamous cell carcinomas (OPSCC).
dc.language.isoenen
dc.rightsArchived with thanks to Oncotargeten
dc.titleDistinct patterns of infiltrating CD8+ T cells in HPV+ and CD68 macrophages in HPV- oropharyngeal squamous cell carcinomas are associated with better clinical outcome but PD-L1 expression is not prognostic.en
dc.typeArticleen
dc.contributor.departmentTranslational Radiobiology Group, Division of Molecular & Clinical Cancer Sciences, School of Medical Sciences, Faculty of Biology, Medicine and Health, University of Manchester, Manchester Academic Health Science Centre, Christie Hospital NHS Trust, Manchesteren
dc.identifier.journalOncotargeten
refterms.dateFOA2018-12-17T14:48:09Z
html.description.abstractImmunotherapies are beginning to revolutionise treatment paradigms in oncology with monoclonal antibodies (mAb) targeting T-cell co-inhibitory (e.g. PD-1/PD-L1) and co-stimulatory pathways (e.g. CTLA-4/CD28) demonstrating clinical utility. Some clinical studies demonstrate that responsiveness to PD-1/PD-L1 mAb therapy is greater in patients with expression of PD-L1 in the tumour microenvironment. However, robust responses have also been observed in patients with low or absent expression of PD-L1. Using multiplex immuno-fluorescent labelling we sought to determine how infiltration of tumours by CD8+ T-cells, their expression of PD-1, and the expression of PD-L1 on both tumours and CD68 cells (macrophages) correlated with HPV status and outcome in a cohort of 124 oropharyngeal squamous cell carcinomas (OPSCC).


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