Harnessing Innate Immunity Using Biomaterials for Cancer Immunotherapy

被引:52
作者
Lee, DaeYong [1 ]
Huntoon, Kristin [1 ]
Wang, Yifan [2 ,3 ]
Jiang, Wen [2 ,3 ]
Kim, Betty Y. S. [1 ]
机构
[1] Univ Texas MD Anderson Canc Ctr, Dept Neurosurg, Houston, TX 77030 USA
[2] Univ Texas Southwestern Med Ctr Dallas, Dept Radiat Oncol, Dallas, TX 75390 USA
[3] Univ Texas MD Anderson Canc Ctr, Dept Radiat Oncol, Houston, TX 77030 USA
关键词
adaptive immunity; biomaterials; cancer immunotherapy; innate immunity; TUMOR-ASSOCIATED MACROPHAGES; IMMUNOGENIC CELL-DEATH; NATURAL-KILLER-CELLS; CGAS-STING PATHWAY; TARGETING DENDRITIC CELLS; DRUG-DELIVERY SYSTEMS; LYMPH-NODE; IN-VIVO; PHOTOTHERMAL THERAPY; ANTITUMOR IMMUNITY;
D O I
10.1002/adma.202007576
中图分类号
O6 [化学];
学科分类号
0703 ;
摘要
The discovery of immune checkpoint blockade has revolutionized the field of immuno-oncology and established the foundation for developing various new therapies that can surpass conventional cancer treatments. Most recent immunotherapeutic strategies have focused on adaptive immune responses by targeting T cell-activating pathways, genetic engineering of T cells with chimeric antigen receptors, or bispecific antibodies. Despite the unprecedented clinical success, these T cell-based treatments have only benefited a small proportion of patients. Thus, the need for the next generation of cancer immunotherapy is driven by identifying novel therapeutic molecules or new immunoengineered cells. To maximize the therapeutic potency via innate immunogenicity, the convergence of innate immunity-based therapy and biomaterials is required to yield an efficient index in clinical trials. This review highlights how biomaterials can efficiently reprogram and recruit innate immune cells in tumors and ultimately initiate activation of T cell immunity against advanced cancers. Moreover, the design and specific biomaterials that improve innate immune cells' targeting ability to selectively activate immunogenicity with minimal adverse effects are discussed.
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页数:35
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