4.8 Article

Nanoengineered Immune Niches for Reprogramming the Immunosuppressive Tumor Microenvironment and Enhancing Cancer Immunotherapy

期刊

ADVANCED MATERIALS
卷 31, 期 34, 页码 -

出版社

WILEY-V C H VERLAG GMBH
DOI: 10.1002/adma.201803322

关键词

antitumor immunity; cancer immunotherapy; immunosuppression; nanoengineered immune niches; tumor microenvironment

资金

  1. National Research Foundation of Korea (NRF) - Korean government [2017R1A2A1A17069277, 2017R1A5A1014560]
  2. National Research Council of Science AMP
  3. Technology (NST) grant - Korea government (MSIT) [CAP-18-02-KRIBB]
  4. National Research Council of Science & Technology (NST), Republic of Korea [CAP-18-02-KRIBB] Funding Source: Korea Institute of Science & Technology Information (KISTI), National Science & Technology Information Service (NTIS)
  5. National Research Foundation of Korea [2017R1A5A1014560, 2017R1A2A1A17069277] Funding Source: Korea Institute of Science & Technology Information (KISTI), National Science & Technology Information Service (NTIS)

向作者/读者索取更多资源

Cancer immunotherapies that harness the body's immune system to combat tumors have received extensive attention and become mainstream strategies for treating cancer. Despite promising results, some problems remain, such as the limited patient response rate and the emergence of severe immune-related adverse effects. For most patients, the therapeutic efficacy of cancer immunotherapy is mainly limited by the immunosuppressive tumor microenvironment (TME). To overcome such obstacles in the TME, the immunomodulation of immunosuppressive factors and therapeutic immune cells (e.g., T cells and antigen-presenting cells) should be carefully designed and evaluated. Nanoengineered synthetic immune niches have emerged as highly customizable platforms with a potent capability for reprogramming the immunosuppressive TME. Here, recent developments in nano-biomaterials that are rationally designed to modulate the immunosuppressive TME in a spatiotemporal manner for enhanced cancer immunotherapy which are rationally designed to modulate the immunosuppressive TME in a spatiotemporal manner for enhanced cancer immunotherapy are highlighted.

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