TLR4型
败血症
炎症
先天免疫系统
特里夫
医学
Toll样受体
药品
受体
体内
免疫学
信号转导
药理学
免疫系统
生物
细胞生物学
内科学
生物技术
作者
Nikolay Kuzmich,К. В. Сивак,Vladimir N. Chubarev,Yuri B. Porozov,T. N. Savateeva-Lyubimova,Francesco Peri
出处
期刊:Vaccines
[MDPI AG]
日期:2017-10-04
卷期号:5 (4): 34-34
被引量:588
标识
DOI:10.3390/vaccines5040034
摘要
Toll-Like Receptor 4 (TLR4) signal pathway plays an important role in initiating the innate immune response and its activation by bacterial endotoxin is responsible for chronic and acute inflammatory disorders that are becoming more and more frequent in developed countries. Modulation of the TLR4 pathway is a potential strategy to specifically target these pathologies. Among the diseases caused by TLR4 abnormal activation by bacterial endotoxin, sepsis is the most dangerous one because it is a life-threatening acute system inflammatory condition that still lacks specific pharmacological treatment. Here, we review molecules at a preclinical or clinical phase of development, that are active in inhibiting the TLR4-MyD88 and TLR4-TRIF pathways in animal models. These are low-molecular weight compounds of natural and synthetic origin that can be considered leads for drug development. The results of in vivo studies in the sepsis model and the mechanisms of action of drug leads are presented and critically discussed, evidencing the differences in treatment results from rodents to humans.
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