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Nanoparticle-Based Immunotherapy for Cancer

期刊

ACS NANO
卷 9, 期 1, 页码 16-30

出版社

AMER CHEMICAL SOC
DOI: 10.1021/nn5062029

关键词

cancer immunotherapy; tumor immune surveillance; tumor immune evasion; tumor immunoediting; tumor-associated antigens; danger-associated molecular patterns; T-lymphocytes; lymphocyte co-stimulators; vaccines; nanoparticles; targeted delivery; environment-responsive nanoparticles

资金

  1. Canadian Institutes of Health Research (CIHR)
  2. Natural Sciences and Engineering Research Council of Canada (NSERC)
  3. Diabetes Research Foundation (DRF)
  4. Juvenile Diabetes Research Foundation (JDRF)
  5. Canadian Diabetes Association (CDA)
  6. Multiple Sclerosis Society of Canada (MSSC)
  7. Brawn Family Foundation
  8. Sarda Farriol Research Programme
  9. European Community's Seventh Framework Programme (EC FP7) [229673]
  10. Eyes' High/Alberta Innovates-Technology Futures postdoctoral fellowship
  11. AXA Research Fund
  12. endMS network
  13. Alberta Heritage Foundation of Medical Research (AHFMR)
  14. Diabetes Association (Foothills)
  15. CDA

向作者/读者索取更多资源

The design of nanovaccines capable of triggering effective antitumor immunity requires an understanding of how the immune system senses and responds to threats, including pathogens and tumors. Equally important is an understanding of the mechanisms employed by tumor cells to evade immunity and an appreciation of the deleterious effects that antitumor immune responses can have on tumor growth, such as by skewing tumor cell composition toward immunologically silent tumor cell variants. The immune system and tumors engage in a tug-of-war driven by competition where promoting antitumor immunity or tumor cell death alone may be therapeutically insufficient. Nanotechnology affords a unique opportunity to develop therapeutic compounds than can simultaneously tackle both aspects, favoring tumor eradication. Here, we review the current status of nanoparticle-based immunotherapeutic strategies for the treatment of cancer, ranging from antigen/adjuvant delivery vehicles (to professional antigen-presenting cell types of the immune system) to direct tumor antigen-specific T-lymphocyte-targeting compounds and their combinations thereof.

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