Therapeutic Interventions Targeting Innate Immune Receptors: A Balancing Act

被引:13
作者
Cao, Xujun [1 ,2 ]
Cordova, Anthony F. [1 ,3 ]
Li, Lingyin [1 ,4 ]
机构
[1] Stanford Univ, ChEM H Inst, Stanford, CA 94305 USA
[2] Stanford Univ, Dept Chem, Stanford, CA 94305 USA
[3] Stanford Univ, Canc Biol Program, Stanford, CA 94305 USA
[4] Stanford Univ, Dept Biochem, Stanford, CA 94305 USA
关键词
CYCLIC GMP-AMP; T-CELL RESPONSES; NF-KAPPA-B; APOPTOSIS INHIBITORY PROTEIN; BACILLUS-CALMETTE-GUERIN; CLASS-II TRANSACTIVATOR; HUMAN DENDRITIC CELLS; DNA SENSOR CGAS; GENERALIZED ARTERIAL CALCIFICATION; NLRP3 INFLAMMASOME ACTIVATION;
D O I
10.1021/acs.chemrev.1c00716
中图分类号
O6 [化学];
学科分类号
0703 ;
摘要
The innate immune system is an organism's first line of defense against an onslaught of internal and external threats. The downstream adaptive immune system has been a popular target for therapeutic intervention, while there is a relative paucity of therapeutics targeting the innate immune system. However, the innate immune system plays a critical role in many human diseases, such as microbial infection, cancer, and autoimmunity, highlighting the need for ongoing therapeutic research. In this review, we discuss the major innate immune pathways and detail the molecular strategies underpinning successful therapeutics targeting each pathway as well as previous and ongoing efforts. We will also discuss any recent discoveries that could inform the development of novel therapeutic strategies. As our understanding of the innate immune system continues to develop, we envision that therapies harnessing the power of the innate immune system will become the mainstay of treatment for a wide variety of human diseases.
引用
收藏
页码:3414 / 3458
页数:45
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