4.7 Review

Polymeric Nanosystems for Immunogenic Cell Death-Based Cancer Immunotherapy

Journal

MACROMOLECULAR BIOSCIENCE
Volume 21, Issue 7, Pages -

Publisher

WILEY-V C H VERLAG GMBH
DOI: 10.1002/mabi.202100075

Keywords

cancer immunotherapy; immunogenic cell death; polymer nanoparticles

Funding

  1. National Natural Science Foundation of China [31771048, 32071350]
  2. Fundamental Research Funds for the Central Universities [2232018A3-07, 2232019A3-06]
  3. International Cooperation Fund of the Science and Technology Commission of Shanghai Municipality [19440741600]

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Immunotherapy has shown a promising direction for cancer treatment by regulating the anti-cancer immune system through immunogenic cancer cell death (ICD). Polymer nanoparticles play a critical role in delivering antigens or immune inducers for ICD-based immunotherapy with their controllable size and excellent biocompatibility.
Immunotherapy has pointed out a scientific and promising direction for cancer treatment through the rouse of immunosurveillance and the decrease of possible side effects in recent years. In immunotherapy, immunogenic cancer cell death (ICD) plays a critical role in regulating anti-cancer immune system in vivo via the release of damage-associated molecular patterns. ICD can not only induce in situ cancer cells apoptosis, but also arouse the immune response against metastatic tumors, which is of great clinical significance to eradicate tumors. In cancer immunotherapy, polymer nanoparticles have drawn increasing attention as an important component of ICD-based immunotherapy attributing to their controllable size, excellent biocompatibility, promising ability of protecting cargo from surrounding environment, which delivers the antigens or immune inducers to antigen-presenting cells, and further triggers sinnvoll T cell response. In this review, the recent advances in the development of polymeric material-based nanosystems for ICD-mediated cancer immunotherapy are summarized. The mechanism of ICD and some current restrictions inhibiting the efficiency of immunotherapy and future prospects are also discussed.

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