Pharmacological modulation of nucleic acid sensors - therapeutic potential and persisting obstacles

被引:128
作者
Vanpouille-Box, Claire [1 ,2 ]
Hoffmann, Jules A. [3 ,4 ,5 ]
Galluzzi, Lorenzo [1 ,2 ,6 ,7 ]
机构
[1] Weill Cornell Med Coll, Dept Radiat Oncol, New York, NY 10065 USA
[2] Sandra & Edward Meyer Canc Ctr, New York, NY 10065 USA
[3] Univ Strasbourg, Inst Adv Studies, Strasbourg, France
[4] Inst Mol & Cellular Biol, CNRS UPR 9022, Strasbourg, France
[5] Guangzhou Med Univ, Sino French Hoffmann Inst, Guangzhou, Guangdong, Peoples R China
[6] Yale Sch Med, Dept Dermatol, New Haven, CT 06510 USA
[7] Univ Paris 05, Paris, France
关键词
TOLL-LIKE RECEPTORS; DOUBLE-STRANDED-RNA; POLYRIBOINOSINIC-POLYRIBOCYTIDYLIC ACID; PHASE-II TRIAL; SYSTEMIC-LUPUS-ERYTHEMATOSUS; AICARDI-GOUTIERES-SYNDROME; PLACEBO-CONTROLLED TRIAL; INNATE IMMUNE-RESPONSES; HEPATITIS-C VIRUS; GMP-AMP SYNTHASE;
D O I
10.1038/s41573-019-0043-2
中图分类号
Q81 [生物工程学(生物技术)]; Q93 [微生物学];
学科分类号
071005 ; 0836 ; 090102 ; 100705 ;
摘要
Nucleic acid sensors, primarily TLR and RLR family members, as well as cGAS-STING signalling, play a critical role in the preservation of cellular and organismal homeostasis. Accordingly, deregulated nucleic acid sensing contributes to the origin of a diverse range of disorders, including infectious diseases, as well as cardiovascular, autoimmune and neoplastic conditions. Accumulating evidence indicates that normalizing aberrant nucleic acid sensing can mediate robust therapeutic effects. However, targeting nucleic acid sensors with pharmacological agents, such as STING agonists, presents multiple obstacles, including drug-, target-, disease- and host-related issues. Here, we discuss preclinical and clinical data supporting the potential of this therapeutic paradigm and highlight key limitations and possible strategies to overcome them.
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页码:845 / 867
页数:23
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