TLR4 Signaling Pathway Modulators as Potential Therapeutics in Inflammation and Sepsis

被引:647
作者
Kuzmich, Nikolay N. [1 ,2 ]
Sivak, Konstantin V. [1 ]
Chubarev, Vladimir N. [3 ]
Porozov, Yury B. [2 ,4 ]
Savateeva-Lyubimova, Tatiana N. [1 ]
Peri, Francesco [5 ]
机构
[1] WHO Natl Influenza Ctr Russia, Res Inst Influenza, Dept Drug Safety, 15-17 Prof Popov St, St Petersburg 197376, Russia
[2] IM Sechenov First Moscow State Med Univ, Inst Pharm & Translat Med, Lab Bioinformat, 8-2 Trubetskaya St, Moscow 119991, Russia
[3] IM Sechenov First Moscow State Med Univ, Inst Pharm & Translat Med, Dept Pharmacol, 8-2 Trubetskaya St, Moscow 119991, Russia
[4] ITMO Univ, Lab Bioinformat, 49 Kronverkskiy Pr, St Petersburg 197101, Russia
[5] Univ Milano Bicocca, Dept Biotechnol & Biosci, Piazza Sci 2, I-20126 Milan, Italy
基金
欧盟地平线“2020”;
关键词
TLR4; sepsis; LPS; CD14; MD-2; in vivo studies; PAMP; DAMP; NF-KAPPA-B; TOLL-LIKE RECEPTORS; LIPOPOLYSACCHARIDE-INDUCED INFLAMMATION; TRANSDUCTION INHIBITOR TAK-242; ESCHERICHIA-COLI CHALLENGE; GENIPIN ATTENUATES SEPSIS; KINASE; IRAK4; SMALL-MOLECULE; ATRACTYLENOLIDE-I; SPARSTOLONIN B;
D O I
10.3390/vaccines5040034
中图分类号
R392 [医学免疫学]; Q939.91 [免疫学];
学科分类号
071005 [微生物学]; 100108 [医学免疫学];
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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