Nanobiomaterial-based vaccination immunotherapy of cancer
- PMID: 33581608
- DOI: 10.1016/j.biomaterials.2021.120709
Nanobiomaterial-based vaccination immunotherapy of cancer
Abstract
Cancer immunotherapies including cancer vaccines, immune checkpoint blockade or chimeric antigen receptor T cells have been exploited as the attractive treatment modalities in recent years. Among these approaches, cancer vaccines that designed to deliver tumor antigens and adjuvants to activate the antigen presenting cells (APCs) and induce antitumor immune responses, have shown significant efficacy in inhibiting tumor growth, preventing tumor relapse and metastasis. Despite the potential of cancer vaccination strategies, the therapeutic outcomes in preclinical trials are failed to promote their clinical translation, which is in part due to their inefficient vaccination cascade of five critical steps: antigen identification, antigen encapsulation, antigen delivery, antigen release and antigen presentation to T cells. In recent years, it has been demonstrated that various nanobiomaterials hold great potential to enhance cancer vaccination cascade and improve their antitumor performance and reduce the off-target effect. We summarize the cutting-edge advances of nanobiomaterials-based vaccination immunotherapy of cancer in this review. The various cancer nanovaccines including antigen peptide/adjuvant-based nanovaccines, nucleic acid-based nanovaccines as well as biomimetic nanobiomaterials-based nanovaccines are discussed in detail. We also provide some challenges and perspectives associated with the clinical translation of cancer nanovaccines.
Keywords: Antitumor immune response; Biomimetic nanobiomaterials; Cancer immunotherapy; Lymph node-targeting; Nanovaccine.
Copyright © 2021 Elsevier Ltd. All rights reserved.
Similar articles
-
Lymph node-targeting nanovaccines for cancer immunotherapy.J Control Release. 2022 Nov;351:102-122. doi: 10.1016/j.jconrel.2022.09.015. Epub 2022 Sep 20. J Control Release. 2022. PMID: 36115556 Review.
-
Nanovaccines for cancer immunotherapy: Focusing on complex formation between adjuvant and antigen.Int Immunopharmacol. 2023 Apr;117:109887. doi: 10.1016/j.intimp.2023.109887. Epub 2023 Feb 24. Int Immunopharmacol. 2023. PMID: 36841155 Review.
-
Nanovaccine-Based Strategies to Overcome Challenges in the Whole Vaccination Cascade for Tumor Immunotherapy.Small. 2021 Jul;17(28):e2006000. doi: 10.1002/smll.202006000. Epub 2021 Mar 26. Small. 2021. PMID: 33768693 Review.
-
Self-adjuvanting cancer nanovaccines.J Nanobiotechnology. 2022 Jul 26;20(1):345. doi: 10.1186/s12951-022-01545-z. J Nanobiotechnology. 2022. PMID: 35883176 Free PMC article. Review.
-
Recent Advances of Emerging Spleen-Targeting Nanovaccines for Immunotherapy.Adv Healthc Mater. 2023 Sep;12(23):e2300351. doi: 10.1002/adhm.202300351. Epub 2023 Jun 15. Adv Healthc Mater. 2023. PMID: 37289567 Review.
Cited by
-
Nanomedicine-induced pyroptosis for anti-tumor immunotherapy: Mechanism analysis and application prospects.Acta Pharm Sin B. 2025 Jul;15(7):3487-3510. doi: 10.1016/j.apsb.2025.05.021. Epub 2025 May 26. Acta Pharm Sin B. 2025. PMID: 40698137 Free PMC article. Review.
-
Mesoporous Silica Nanoparticles as an Ideal Platform for Cancer Immunotherapy: Recent Advances and Future Directions.Adv Healthc Mater. 2024 Aug;13(20):e2400323. doi: 10.1002/adhm.202400323. Epub 2024 May 3. Adv Healthc Mater. 2024. PMID: 38653190 Free PMC article. Review.
-
Biomineralization-inspired synthesis of autologous cancer vaccines for personalized metallo-immunotherapy.iScience. 2024 Jun 5;27(7):110189. doi: 10.1016/j.isci.2024.110189. eCollection 2024 Jul 19. iScience. 2024. PMID: 38989457 Free PMC article.
-
Modulation of oral vaccine efficacy by the gut microbiota.NPJ Vaccines. 2025 Aug 1;10(1):179. doi: 10.1038/s41541-025-01240-8. NPJ Vaccines. 2025. PMID: 40750603 Free PMC article. Review.
-
A bibliometric insight into nanomaterials in vaccine: trends, collaborations, and future avenues.Front Immunol. 2024 Aug 12;15:1420216. doi: 10.3389/fimmu.2024.1420216. eCollection 2024. Front Immunol. 2024. PMID: 39188723 Free PMC article.
Publication types
MeSH terms
Substances
LinkOut - more resources
Full Text Sources
Other Literature Sources
Medical
Miscellaneous