At The Interface: Small-Molecule Inhibitors of Soluble Cytokines

被引:0
作者
Raavi, Angela N.
Koehler, Angela N. [1 ,2 ,3 ]
Vegas, Arturo J. [4 ]
机构
[1] MIT, Koch Inst Integrat Canc Res, Cambridge, MA 02139 USA
[2] MIT, Dept Biol Engn, Cambridge, MA 02139 USA
[3] Broad Inst MIT & Harvard, Cambridge, MA 02142 USA
[4] Boston Univ, Dept Chem, Boston, MA 02115 USA
关键词
TUMOR-NECROSIS-FACTOR; D-DOPACHROME TAUTOMERASE; THERAPEUTIC MONOCLONAL-ANTIBODIES; INTERLEUKIN-18; BINDING-PROTEIN; INTERFERON-GAMMA PRODUCTION; RHEUMATOID-ARTHRITIS; FACTOR MIF; CRYSTAL-STRUCTURE; DOUBLE-BLIND; ENZYMATIC-ACTIVITY;
D O I
10.1021/acs.chemrev.4c00469
中图分类号
O6 [化学];
学科分类号
0703 ;
摘要
Cytokines are crucial regulators of the immune system that orchestrate interactions between cells and, when dysregulated, contribute to the progression of chronic inflammation, cancer, and autoimmunity. Numerous biologic-based clinical agents, mostly monoclonal antibodies, have validated cytokines as important clinical targets and are now part of the standard of care for a number of diseases. These agents, while impactful, still suffer from limitations including a lack of oral bioavailability, high cost of production, and immunogenicity. Small-molecule cytokine inhibitors are attractive alternatives that can address these limitations. Although targeting cytokine-cytokine receptor complexes with small molecules has been a challenging research endeavor, multiple small-molecule inhibitors have now been identified, with a number of them undergoing clinical evaluation. In this review, we highlight the recent advancements in the discovery and development of small-molecule inhibitors targeting soluble cytokines. The strategies for identifying these novel ligands as well as the structural and mechanistic insights into their activity represent important milestones in tackling these challenging and clinically important protein-protein interactions.
引用
收藏
页码:4528 / 4568
页数:41
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