| Literature DB >> 20484030 |
Vincenzo Cerullo1, Sari Pesonen, Iulia Diaconu, Sophie Escutenaire, Petteri T Arstila, Matteo Ugolini, Petri Nokisalmi, Mari Raki, Leena Laasonen, Merja Särkioja, Maria Rajecki, Lotta Kangasniemi, Kilian Guse, Andreas Helminen, Laura Ahtiainen, Ari Ristimäki, Anne Räisänen-Sokolowski, Elina Haavisto, Minna Oksanen, Eerika Karli, Aila Karioja-Kallio, Sirkka-Liisa Holm, Mauri Kouri, Timo Joensuu, Anna Kanerva, Akseli Hemminki.
Abstract
Granulocyte macrophage colony-stimulating factor (GMCSF) can mediate antitumor effects by recruiting natural killer cells and by induction of tumor-specific cytotoxic T-cells through antigen-presenting cells. Oncolytic tumor cell-killing can produce a potent costimulatory danger signal and release of tumor epitopes for antigen-presenting cell sampling. Therefore, an oncolytic adenovirus coding for GMCSF was engineered and shown to induce tumor-specific immunity in an immunocompetent syngeneic hamster model. Subsequently, 20 patients with advanced solid tumors refractory to standard therapies were treated with Ad5-D24-GMCSF. Of the 16 radiologically evaluable patients, 2 had complete responses, 1 had a minor response, and 5 had disease stabilization. Responses were frequently seen in injected and noninjected tumors. Treatment was well tolerated and resulted in the induction of both tumor-specific and virus-specific immunity as measured by ELISPOT and pentamer analysis. This is the first time that oncolytic virus-mediated antitumor immunity has been shown in humans. Ad5-D24-GMCSF is promising for further clinical testing. Copyright 2010 AACR.Entities:
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Year: 2010 PMID: 20484030 DOI: 10.1158/0008-5472.CAN-09-3567
Source DB: PubMed Journal: Cancer Res ISSN: 0008-5472 Impact factor: 12.701