Synergy of Radiotherapy and a Cancer Vaccine for the Treatment of HPV-Associated Head and Neck Cancer

Michele Mondini(Inserm), Mevyn Nizard(Délégation Paris 5), Thi Tran(Délégation Paris 5), Laëtitia Mauge(Délégation Paris 5), Mauro Loi(Inserm), Céline Clémenson(Inserm), Delphine Dugué(Inserm), Pierre Maroun(Université Paris-Sud), Émilie Louvet(Inserm), Julien Adam(Inserm), Cécile Badoual(Délégation Paris 5), Dominique Helley(Délégation Paris 5), Estelle Dransart(Centre National de la Recherche Scientifique), Ludger Johannes(Centre National de la Recherche Scientifique), Marie‐Catherine Vozenin(Université Paris-Sud), Jean‐Luc Perfettini(Université Paris-Sud), Éric Tartour(Délégation Paris 5), Éric Deutsch(Université Paris-Sud)
Molecular Cancer Therapeutics
April 2, 2015
Cited by 88Open Access
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Abstract

There is growing interest in the association of radiotherapy and immunotherapy for the treatment of solid tumors. Here, we report an extremely effective combination of local irradiation (IR) and Shiga Toxin B (STxB)-based human papillomavirus (HPV) vaccination for the treatment of HPV-associated head and neck squamous cell carcinoma (HNSCC). The efficacy of the irradiation and vaccine association was tested using a model of HNSCC obtained by grafting TC-1/luciferase cells at a submucosal site of the inner lip of immunocompetent mice. Irradiation and the STxB-E7 vaccine acted synergistically with both single and fractionated irradiation schemes, resulting in complete tumor clearance in the majority of the treated mice. A dose threshold of 7.5 Gy was required to elicit the dramatic antitumor response. The combined treatment induced high levels of tumor-infiltrating, antigen-specific CD8(+) T cells, which were required to trigger the antitumor activity. Treatment with STxB-E7 and irradiation induced CD8(+) T-cell memory, which was sufficient to exert complete antitumor responses in both local recurrences and distant metastases. We also report for the first time that a combination therapy based on local irradiation and vaccination induces an increased pericyte coverage (as shown by αSMA and NG2 staining) and ICAM-1 expression on vessels. This was associated with enhanced intratumor vascular permeability that correlated with the antitumor response, suggesting that the combination therapy could also act through an increased accessibility for immune cells. The combination strategy proposed here offers a promising approach that could potentially be transferred into early-phase clinical trials.


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