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Article: Light-responsive nanomedicine for cancer immunotherapy

TitleLight-responsive nanomedicine for cancer immunotherapy
Authors
KeywordsCancer therapy
Immunotherapy
Light-responsive nanoparticles
Light-triggered drug release
Nanomedicine
Photodynamic therapy
Photopharmacology
Photothermal therapy
Issue Date19-May-2023
PublisherElsevier
Citation
Acta Pharmaceutica Sinica B, 2023, v. 13, n. 6, p. 2346-2368 How to Cite?
Abstract

Immunotherapy emerged as a paradigm shift in cancer treatments, which can effectively inhibit cancer progression by activating the immune system. Remarkable clinical outcomes have been achieved through recent advances in cancer immunotherapy, including checkpoint blockades, adoptive cellular therapy, cancer vaccine, and tumor microenvironment modulation. However, extending the application of immunotherapy in cancer patients has been limited by the low response rate and side effects such as autoimmune toxicities. With great progress being made in nanotechnology, nanomedicine has been exploited to overcome biological barriers for drug delivery. Given the spatiotemporal control, light-responsive nanomedicine is of great interest in designing precise modality for cancer immunotherapy. Herein, we summarized current research utilizing light-responsive nanoplatforms to enhance checkpoint blockade immunotherapy, facilitate targeted delivery of cancer vaccines, activate immune cell functions, and modulate tumor microenvironment. The clinical translation potential of those designs is highlighted and challenges for the next breakthrough in cancer immunotherapy are discussed.


Persistent Identifierhttp://hdl.handle.net/10722/340563
ISSN
2023 Impact Factor: 14.7
2023 SCImago Journal Rankings: 3.035
ISI Accession Number ID

 

DC FieldValueLanguage
dc.contributor.authorKang, Weirong-
dc.contributor.authorLiu, Yuwei-
dc.contributor.authorWang, Weiping-
dc.date.accessioned2024-03-11T10:45:32Z-
dc.date.available2024-03-11T10:45:32Z-
dc.date.issued2023-05-19-
dc.identifier.citationActa Pharmaceutica Sinica B, 2023, v. 13, n. 6, p. 2346-2368-
dc.identifier.issn2211-3835-
dc.identifier.urihttp://hdl.handle.net/10722/340563-
dc.description.abstract<p>Immunotherapy emerged as a paradigm shift in cancer treatments, which can effectively inhibit cancer progression by activating the immune system. Remarkable clinical outcomes have been achieved through recent advances in cancer immunotherapy, including checkpoint blockades, adoptive cellular therapy, cancer vaccine, and tumor microenvironment modulation. However, extending the application of immunotherapy in cancer patients has been limited by the low response rate and side effects such as autoimmune toxicities. With great progress being made in nanotechnology, nanomedicine has been exploited to overcome biological barriers for drug delivery. Given the spatiotemporal control, light-responsive nanomedicine is of great interest in designing precise modality for cancer immunotherapy. Herein, we summarized current research utilizing light-responsive nanoplatforms to enhance checkpoint blockade immunotherapy, facilitate targeted delivery of cancer vaccines, activate immune cell functions, and modulate tumor microenvironment. The clinical translation potential of those designs is highlighted and challenges for the next breakthrough in cancer immunotherapy are discussed.<br></p>-
dc.languageeng-
dc.publisherElsevier-
dc.relation.ispartofActa Pharmaceutica Sinica B-
dc.rightsThis work is licensed under a Creative Commons Attribution-NonCommercial-NoDerivatives 4.0 International License.-
dc.subjectCancer therapy-
dc.subjectImmunotherapy-
dc.subjectLight-responsive nanoparticles-
dc.subjectLight-triggered drug release-
dc.subjectNanomedicine-
dc.subjectPhotodynamic therapy-
dc.subjectPhotopharmacology-
dc.subjectPhotothermal therapy-
dc.titleLight-responsive nanomedicine for cancer immunotherapy-
dc.typeArticle-
dc.identifier.doi10.1016/j.apsb.2023.05.016-
dc.identifier.scopuseid_2-s2.0-85163201042-
dc.identifier.volume13-
dc.identifier.issue6-
dc.identifier.spage2346-
dc.identifier.epage2368-
dc.identifier.isiWOS:001027052700001-
dc.identifier.issnl2211-3835-

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