Volume 2 Supplement 2

Abstracts from the 1st Immunotherapy of Cancer Conference (ITOC1)

Open Access

P57. Activation of RIG-I induces immunogenic cell death

  • S Bek1,
  • D Kreppel1,
  • M Bscheider1,
  • CC Lin1,
  • T Haas1 and
  • H Poeck1
Journal for ImmunoTherapy of Cancer20142(Suppl 2):P31

https://doi.org/10.1186/2051-1426-2-S2-P31

Published: 12 March 2014

Background

The interaction between the immune system and cancer cells has become a focus of recent cancer therapy research. Immunogenic cell death, short ICD, was described as a cell death modality that stimulates an immune response against dead-cell antigens, in particular when they derive from cancer cells. Most malignant cells are poorly immunogenic and fail to elicit an effective antitumour immune response. Certain anti-cancer treatments, however, have been shown to induce ICD and transform cancer cells into potent inducers of an anti-cancer immune response. An important component is the induction of a specific cytotoxic T-cell response driven by DCs that have engulfed and processed tumour antigens. Recently, we have shown that the RIG-I ligand 3pRNA induces tumosr cell death in vitro and in vivo. Whether and how 3pRNA induced tumour cell death leads to a specific antitumor response is unknown. Here we analyse the immunogenicity of RIG-I induced tumour cell death in vitro and in vivo.

Material and methods

We induced tumour cell death by treating ovalbumin expressing B16 melanoma cells with 3pRNA. We co-cultured 3pRNA treated B16-OVA cells with splenic DCs and CFSE-labeled OT-I T-cells to analyse a specific T-cell activation and proliferation. Furthermore, we vaccinated 3pRNA treated B16-OVA cells subcutaneously into C57BL/6 mice to analyse their immunogenic potential in vivo. After vaccination, draining lymph node cells are analysed for T-cell activation and IFNg production using flow cytometry.

Results

We show that 3pRNA treatment leads to increased cytokine expression, upregulation of costimulatory molecules, cross-presentation and induction of cell death in B16-OVA melanoma cells in vitro. 3p-RNA treated B16-OVA cells induce proliferation and IFNg production of OT-I T-cells in co-cultures with spleen derived DCs. After subcutaneous injection of 3pRNA killed B16-OVA cells but not live B16-OVA cells into C57BL/6 mice, potent proliferation and IFNg production of antigen specific CD4 and CD8 T cells is seen in the draining lymph node. Overall, these effects were more pronounced after 3pRNA treatment than after Oxaliplatin induced cell death.

Conclusions

3pRNA treatment of tumor cells leads to a potent immunogenic phenotype with induction of antigen-specific T-cell responses both in vitro and in vivo. These findings may have implications for a new therapeutic approach in immune mediated cancer treatment.

Authors’ Affiliations

(1)
Klinikum Rechts der Isar der TU-München, Medizinische Klinik

Copyright

© Bek et al; licensee BioMed Central Ltd. 2014

This article is published under license to BioMed Central Ltd. This is an Open Access article distributed under the terms of the Creative Commons Attribution License (http://creativecommons.org/licenses/by/2.0), which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited. The Creative Commons Public Domain Dedication waiver (http://creativecommons.org/publicdomain/zero/1.0/) applies to the data made available in this article, unless otherwise stated.

Advertisement