4.7 Article

Immunogenic cell death-inducing chemotherapeutic nanoformulations potentiate combination chemoimmunotherapy

Journal

MATERIALS & DESIGN
Volume 202, Issue -, Pages -

Publisher

ELSEVIER SCI LTD
DOI: 10.1016/j.matdes.2021.109465

Keywords

Nanomaterial; Chemotherapeutic agent; Immunogenic cell death; Immunomodulatory factor; Chemoimmunotherapy

Funding

  1. National Natural Science Foundation of China [52022095, 51973216, 51873207, 51803006, 51833010]
  2. Science and Technology Development Program of Jilin Province [20200404182YY]
  3. Youth Innovation Promotion Association of Chinese Academy of Sciences [2019230]

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Nanomedicine-based chemotherapeutic formulations can induce immunogenic cell death, which enhances the effectiveness of combination chemoimmunotherapy. The combination of these formulations with immunoactivating agents is a promising strategy for clinical cancer treatment.
Chemotherapeutic nanoformulations, which can induce the immunogenic death of tumor cells, have attracted in-creasing attention for their abilities to enable and potentiate combination chemoimmunotherapy. Immunogenic cell death (ICD) causes the release of tumor-associated antigens, tumor-specific antigens, danger-associated mo-lecular patterns, and pro-inflammatory cytokines, which trigger adaptive immune cells to elicit an antitumor immune response. The combination of ICD-inducing nanomedicines and immunoactivators represents a promising strategy for enhancing chemoimmunotherapy in clinical applications. In this review, we provide an overview of the latest advances in chemotherapeutic nanoformulation-mediated immune activation and the combination strategies with various immunoactivating agents, such as immune checkpoint inhibitors, indoleamine 2,3-dioxygenase inhibitors, cytokines, and Toll-like receptor agonists, and predict their potential to contribute significantly to clinical cancer chemoimmunotherapy. (c) 2021 The Author(s). Published by Elsevier Ltd. This is an open access article under the CC BY-NC-ND license (http://creativecommons.org/licenses/by-nc-nd/4.0/).

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