4.7 Review

Extracellular Vesicles as an Advanced Delivery Biomaterial for Precision Cancer Immunotherapy

Journal

ADVANCED HEALTHCARE MATERIALS
Volume 11, Issue 5, Pages -

Publisher

WILEY
DOI: 10.1002/adhm.202100650

Keywords

cancer immunotherapy; delivery biomaterials; exosomes; extracellular vesicles

Funding

  1. NIH NIGMS MIRA award [1R35GM133794]
  2. USDA-NIFA [2017-67021-26600]

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Cancer immunotherapy has shown benefits in recent years, but novel targeting approaches and modulators are needed for broader patient populations. Extracellular vesicles (EVs) offer targeted immunity modulation and improved efficacy, with unique properties like surface markers and immunomodulatory functions. Future potential lies in EVs as a cancer immunotherapeutic biomaterial through reprogramming strategies and addressing unique challenges.
In recent years, cancer immunotherapy has been observed in numerous preclinical and clinical studies for showing benefits. However, due to the unpredictable outcomes and low response rates, novel targeting delivery approaches and modulators are needed for being effective to more broader patient populations and cancer types. Compared to synthetic biomaterials, extracellular vesicles (EVs) specifically open a new avenue for improving the efficacy of cancer immunotherapy by offering targeted and site-specific immunity modulation. In this review, the molecular understanding of EV cargos and surface receptors, which underpin cell targeting specificity and precisely modulating immunogenicity, are discussed. Unique properties of EVs are reviewed in terms of their surface markers, intravesicular contents, intrinsic immunity modulatory functions, and pharmacodynamic behavior in vivo with tumor tissue models, highlighting key indications of improved precision cancer immunotherapy. Novel molecular engineered strategies for reprogramming and directing cancer immunotherapeutics, and their unique challenges are also discussed to illuminate EV's future potential as a cancer immunotherapeutic biomaterial.

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