Nanosized drug delivery systems modulate the immunosuppressive microenvironment to improve cancer immunotherapy
Acta Pharmacologica Sinica, ISSN: 1745-7254, Vol: 43, Issue: 12, Page: 3045-3054
2022
- 17Citations
- 12Captures
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Example: if you select the 1-year option for an article published in 2019 and a metric category shows 90%, that means that the article or review is performing better than 90% of the other articles/reviews published in that journal in 2019. If you select the 3-year option for the same article published in 2019 and the metric category shows 90%, that means that the article or review is performing better than 90% of the other articles/reviews published in that journal in 2019, 2018 and 2017.
Citation Benchmarking is provided by Scopus and SciVal and is different from the metrics context provided by PlumX Metrics.
Metrics Details
- Citations17
- Citation Indexes17
- 17
- CrossRef2
- Captures12
- Readers12
- 12
Review Description
Immunotherapy that activates immune systems for combating cancer has yielded considerable clinical benefits recently. However, the immunosuppressive tumor microenvironment (ITME) is a major hurdle to immunotherapy as it supports tumor to evade immune surveillance. Reversing ITME facilitates the recruitment and activation of antitumor immune cells, thereby promoting immunotherapy. Our group has developed various nanosized drug delivery systems (NDDSs) to modulate ITME with enhanced efficacy and safety. In the review we introduce the ITME-remodeling strategies for improving immunotherapy based on NDDSs including triggering tumor cells to undergo immunogenetic cell death (ICD), applying tumor vaccine, and directly regulating intratumoral immune components (immune cells or cytokines). In order to guide the design of NDDSs for amplified effects of antitumor immunotherapy, the contributions and future directions of this field are also discussed.
Bibliographic Details
http://www.scopus.com/inward/record.url?partnerID=HzOxMe3b&scp=85137065384&origin=inward; http://dx.doi.org/10.1038/s41401-022-00976-6; http://www.ncbi.nlm.nih.gov/pubmed/36050519; https://www.nature.com/articles/s41401-022-00976-6; http://sciencechina.cn/gw.jsp?action=cited_outline.jsp&type=1&id=7371381&internal_id=7371381&from=elsevier; https://dx.doi.org/10.1038/s41401-022-00976-6
Springer Science and Business Media LLC
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