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      NK-Cell Recruitment Is Necessary for Eradication of Peritoneal Carcinomatosis with an IL12-Expressing Maraba Virus Cellular Vaccine.

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          Abstract

          Despite improvements in chemotherapy and radical surgical debulking, peritoneal carcinomatosis (PC) remains among the most common causes of death from abdominal cancers. Immunotherapies have been effective for selected solid malignancies, but their potential in PC has been little explored. Here, we report that intraperitoneal injection of an infected cell vaccine (ICV), consisting of autologous tumor cells infected ex vivo with an oncolytic Maraba MG1 virus expressing IL12, promotes the migration of activated natural killer (NK) cells to the peritoneal cavity in response to the secretion of IFNγ-induced protein-10 (IP-10) from dendritic cells. The recruitment of cytotoxic, IFNγ-secreting NK cells was associated with reduced tumor burden and improved survival in a colon cancer model of PC. Even in mice with bulky PC (tumors > 8 mm), a complete radiologic response was demonstrated within 8 to14 weeks, associated with 100% long-term survival. The impact of MG1-IL12-ICV upon NK-cell recruitment and function observed in the murine system was recapitulated in human lymphocytes exposed to human tumor cell lines infected with MG1-IL12. These findings suggest that an MG1-IL12-ICV is a promising therapy that could provide benefit to the thousands of patients diagnosed with PC each year. Cancer Immunol Res; 5(3); 211-21. ©2017 AACR.

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          Author and article information

          Journal
          Cancer Immunol Res
          Cancer immunology research
          American Association for Cancer Research (AACR)
          2326-6074
          2326-6066
          Mar 2017
          : 5
          : 3
          Affiliations
          [1 ] Centre for Innovative Cancer Research, Ottawa Hospital Research Institute.
          [2 ] Department of Laboratory Medicine, University of Tabuk, Tabuk, Saudi Arabia.
          [3 ] Department of BMI, University of Ottawa, Ottawa, Ontario, Canada.
          [4 ] Apoptosis Research Centre, CHEO Research Institute, Ottawa, Ontario, Canada.
          [5 ] Department of Medical Technology, Taibah University, Medina, Saudi Arabia.
          [6 ] Department of Medical Imaging, University of Ottawa, Ottawa, Ontario, Canada.
          [7 ] Department of Radiology, University of Ottawa, Ottawa, Ontario, Canada.
          [8 ] Department of Pathology and Laboratory Medicine, University of Ottawa, Ottawa, Ontario, Canada.
          [9 ] Centre for Innovative Cancer Research, Ottawa Hospital Research Institute. rauer@toh.ca.
          [10 ] Department of Surgery, University of Ottawa, Ottawa, Ontario, Canada.
          Article
          2326-6066.CIR-16-0162
          10.1158/2326-6066.CIR-16-0162
          28159747
          0776499f-9ea3-4585-b041-1b60630b5842
          History

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