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Review
. 2020 Jan 17:10:2935.
doi: 10.3389/fimmu.2019.02935. eCollection 2019.

A Role for Dogs in Advancing Cancer Immunotherapy Research

Affiliations
Review

A Role for Dogs in Advancing Cancer Immunotherapy Research

Steven Dow. Front Immunol. .

Abstract

While rodent cancer models are essential for early proof-of-concept and mechanistic studies for immune therapies, these models have limitations with regards to predicting the ultimate effectiveness of new immunotherapies in humans. As a unique spontaneous, large animal model of cancer, the value of conducting studies in pet dogs with cancer has been increasingly recognized by the research community. This review will therefore summarize key aspects of the dog cancer immunotherapy model and the role that these studies may play in the overall immunotherapy drug research effort. We will focus on cancer types and settings in which the dog model is most likely to impact clinical immuno-oncology research and drug development. Immunological reagent availability is discussed, along with some unique opportunities and challenges associated with the dog immunotherapy model. Overall it is hoped that this review will increase awareness of the dog cancer immunotherapy model and stimulate additional collaborative studies to benefit both man and man's best friend.

Keywords: canine; cell; cytokine; immune; oncology.

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Figures

Figure 1
Figure 1
Tumor response to TME modification with a T cell activator. A dog with oral malignant melanoma (left panel) was treated with a series of every 2 week intratumoral injections of plasmid DNA encoding a bacterial superantigen gene (SEB), along with an IL-2 encoding plasmid. Tumor depigmentation was evident after the first injection (middle image) and complete tumor regression was noted after the second intratumoral injection (right panel).

References

    1. Wege AK. Humanized mouse models for the preclinical assessment of cancer immunotherapy. BioDrugs. (2018) 32:245–66. 10.1007/s40259-018-0275-4 - DOI - PubMed
    1. Garden OA, Volk SW, Mason NJ, Perry JA. Companion animals in comparative oncology: one Medicine in action. Vet J. (2018) 240:6–13. 10.1016/j.tvjl.2018.08.008 - DOI - PubMed
    1. Park JS, Withers SS, Modiano JF, Kent MS, Chen M, Luna JI, et al. Canine cancer immunotherapy studies: linking mouse and human. J Immunother Cancer. (2016) 4:97. 10.1186/s40425-016-0200-7 - DOI - PMC - PubMed
    1. Withrow SJ, Khanna C. Bridging the gap between experimental animals and humans in osteosarcoma. Cancer Treat Res. (2009) 152:439–46. 10.1007/978-1-4419-0284-9_24 - DOI - PubMed
    1. Buque A, Galluzzi L. Modeling tumor immunology and immunotherapy in mice. Trends Cancer. (2018) 4:599–601. 10.1016/j.trecan.2018.07.003 - DOI - PubMed

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