Abstract

Tumor-derived extracellular vesicles (TEVs) are important regulators of the immune response in cancer; however, most research so far has been carried out using cell culture systems. Immune-competent murine tumor models currently provide the best platform to assess proposed roles of TEVs using in vivo animal models and therefore are important for examining interactions between TEVs and the immune system. In this review, we present the current knowledge on TEVs using in vivo tumor-bearing animal models, with a focus on the role of TEVs in mediating crosstalk between tumor cells and both adaptive and innate immune cells. In particular, we address the question how animal models can clarify the reported heterogeneity of TEV effects in both anti-tumor responses and evasion of immune surveillance. The potential of TEVs in mediating direct antigen-presenting functions supports their potential as cancer vaccine therapeutics, therefore, we provide an overview of key findings of TEV trials that have the potential as novel immunotherapies, and shed light on challenges in the path toward the first in-human trials. We also highlight the important updates on the methods that continue to enhance the rigor and reproducibility of EV studies, particularly in functional animal models.

Highlights

  • Metastatic cancers are among the deadliest diseases worldwide, yet, therapy options remain limited

  • The importance of an immune-competent model is highlighted by the need to understand tumor-immune cellcrosstalk mediated by Tumor-derived extracellular vesicles (TEVs) in the complexity of an animal model, which we argue have the greatest potential to provide insight into the TEV-dependent mechanisms relevant to metastasis and translation to humans

  • As substantial progress has been recently made especially in the field of nanotechnology, further advances in nanoscale bioimaging might enable rigorous animal trials, which could elucidate the enigmatic dichotomy of TEV functions in cancer immunity

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Summary

INTRODUCTION

Metastatic cancers are among the deadliest diseases worldwide, yet, therapy options remain limited. Another study reported that treatment of tumor cells with IFN-g results in the release of TEVs which have the capacity to induce IL-12 secretion in cultured DCs, promoting tumor surveillance [38] This is interesting as this effect was attributed to TEV-associated HSP72, which has been described by other groups as an inducer of pro-tumoral phenotypes in DCs [37]. This effect might be due to the uptake of vesicular RNA that exerts signaling functions or the uptake of circulating oncogenic DNA [63] These findings underline the potential of deciphering TEV-based mechanisms by which neutrophils are altered toward a phenotype that promotes tumor survival and progression

A PERSPECTIVE ON TEVS IN IMMUNOTHERAPY AND BIOENGINEERING
CONCLUDING REMARKS
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