4.8 Review

Advanced nanovaccines based on engineering nanomaterials for accurately enhanced cancer immunotherapy

Journal

COORDINATION CHEMISTRY REVIEWS
Volume 472, Issue -, Pages -

Publisher

ELSEVIER SCIENCE SA
DOI: 10.1016/j.ccr.2022.214788

Keywords

Nanovaccine; Antigen presentation processing; Cancer immunotherapy; Dendritic cells-targeting; Antigen delivery; Immune activations

Funding

  1. Natural Science Foundation of China [81773183, 21705120]
  2. Technology Support Project of Shandong Province Higher Educational Youth Innovation [2019KJM008]
  3. Royal College of Surgeons in Ireland (RCSI) [R21393A07]
  4. China Scholarship Council (CSC) [[2021] 395]
  5. National Research Foundation of Korea [2018R1A3B1052702, 2019M3E5D1A01068998]
  6. National Research Foundation of Korea [2019M3E5D1A01068998] Funding Source: Korea Institute of Science & Technology Information (KISTI), National Science & Technology Information Service (NTIS)

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Nanovaccines based on nanomaterials have emerged as an advanced technology for enhancing anti-tumor immunotherapy. They stimulate antigen presenting cells to release signals and activate immune-killing T cells, improving the efficacy of immunotherapy. The positive regulation of nanovaccines enhances antigen presentation and recruits more immune-killing T cells.
In recent years, nanovaccine based on nanomaterials emerging as an advanced nanotechnology has drawn more attention for accurately enhancing anti-tumor immunotherapy. Nanovaccine loaded with antigen and immunopotentiator could stimulate antigen presenting cells (APCs) to release signals of co-stimulatory cytokines and reinvigorate the immune-killing T cell to alleviate tumor progression. The amplification of co-stimulatory markers has the potential to enhance the sensitivity of APCs towards tumor neoantigens. Furthermore, positive regulation via nanovaccine of antigen-dependent APCs with a self-promoting effect with more recruits of immune-killing T cells could contribute to potentiating the presentation and processing of antigen, finally improving the efficacy of immunotherapy. Of note, if the intracellular and exocellular delivery of antigen could be effectively manipulated, the well-designed nanovaccine will provide a platform for clinical therapeutic practice. In this review, we summarize the development, technical advantages and challenges of nanovaccine in the multi-stage delivery process for immune-guided therapeutic efficacy.

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