Interleukin-1 receptor associated kinase inhibitors: Potential therapeutic agents for inflammatory- and immune-related disorders

被引:63
作者
Bahia, Malkeet Singh [1 ]
Kaur, Maninder [1 ]
Silakari, Pragati [1 ]
Silakari, Om [1 ]
机构
[1] Punjabi Univ, Dept Pharmaceut Sci & Drug Res, Mol Modeling Lab MML, Patiala 147002, Punjab, India
关键词
Interleukin-1 receptor associated kinase-4 (IRAK-4); Inflammation; Toll-like receptors; TLR/IL-1 receptor (TIR) superfamily; MyD88-dependent and independent pathways; NF-KAPPA-B; TOLL-LIKE RECEPTORS; DOMAIN-CONTAINING ADAPTER; IL-1; RECEPTOR; CRYSTAL-STRUCTURE; IRAK-4; INHIBITORS; CUTTING EDGE; STRUCTURAL BASIS; PEPTIDE SUBSTRATE; ACTIVATION;
D O I
10.1016/j.cellsig.2015.02.025
中图分类号
Q2 [细胞生物学];
学科分类号
071013 [干细胞生物学];
摘要
The various cells of innate immune system quickly counter-attack invading pathogens, and mount up "first line" defense through their trans-membrane receptors including Toll-like receptors (TLRs) and interleukin receptors (IL-Rs) that result in the secretion of pro-inflammatory cytokines. Albeit such inflammatory responses are beneficial in pathological conditions, their overstimulation may cause severe inflammatory damage; thus, make this defense system a "double edged sword". IRAK-4 has been evaluated as an indispensable element of IL-Rs and TLR pathways that can regulate the abnormal levels of cytokines, and therefore could be employed to manage immune- and inflammation-related disorders. Historically, the identification of selective and potent inhibitors has been challenging; thus, a limited number of small molecule IRAK-4 inhibitors are available in literature. Recently, IRAK-4 achieved great attention, when Ligand (R) pharmaceutical and Nimbus Discovery (R) reported the beneficial potentials of IRAK-4 inhibitors in the pre-clinical evaluation for various inflammatory- and immune-related disorders, but not limited to, such as rheumatoid arthritis, inflammatory bowel disease, psoriasis, gout, asthma and cancer. (C) 2015 Elsevier Inc. All rights reserved.
引用
收藏
页码:1039 / 1055
页数:17
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