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Tumor-Derived Exosomes: The Next Generation of Promising Cell-Free Vaccines in Cancer Immunotherapy Publisher Pubmed



Naseri M1, 2 ; Bozorgmehr M2 ; Zoller M3 ; Ranaei Pirmardan E4 ; Madjd Z1, 2
Authors
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Authors Affiliations
  1. 1. Department of Molecular Medicine, Faculty of Advanced Technologies in Medicine, Iran University of Medical Sciences, Tehran, Iran
  2. 2. Oncopathology Research Center, Iran University of Medical Sciences, Tehran, Iran
  3. 3. Section Pancreas Research, University Hospital of Surgery, Heidelberg, Germany
  4. 4. Molecular Biomarkers Nano-imaging Laboratory, Brigham & Women’s Hospital, Department of Radiology, Harvard Medical School, Boston, MA, United States

Source: OncoImmunology Published:2020


Abstract

Identification of immunogenic tumor antigens that are efficiently processed and delivered by dendritic cells to prime the immune system and to induce an appropriate immune response is a research hotspot in the field of cancer vaccine development. High biosafety is an additional demand. Tumor-derived exosomes (TEXs) are nanosized lipid bilayer encapsulated vesicles that shuttle bioactive information to the tumor microenvironment facilitating tumor progression. However, accumulating evidence points toward the capacity of TEXs to efficiently stimulate immune responses against tumors provided they are appropriately administered. After briefly describing the function of exosomes in cancer biology and their communication with immune cells, we summarize in this review in vitro and preclinical studies eliciting the potency of TEXs in inducing effective anti-tumor responses and recently modified strategies further improving TEX-vaccination efficacy. We interpret the available data as TEXs becoming a lead in cancer vaccination based on tumor antigen-selective high immunogenicity. © 2020, © 2020 The Author(s). Published with license by Taylor & Francis Group, LLC.
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