前激肽释放酶
缓激肽
化学
激肽释放酶
生物化学
酶
受体
作者
Jason D. Ferrone,Gourab Bhattacharjee,Alexey S. Revenko,Thomas Zanardi,Marshelle Warren,Frederick J. Derosier,Nicholas J. Viney,Nguyen C. Pham,Gwendolyn E. Kaeser,Brenda F. Baker,Eugene Schneider,Steven G. Hughes,Brett P. Monia,A. Robert MacLeod
出处
期刊:Nucleic Acid Therapeutics
[Mary Ann Liebert]
日期:2019-04-01
卷期号:29 (2): 82-91
被引量:27
标识
DOI:10.1089/nat.2018.0754
摘要
Kallikrein is the key contact system mediator responsible for the conversion of high-molecular-weight kininogen into the inflammatory vasodilator peptide bradykinin, a process regulated by C1-esterase inhibitor (C1-INH). In hereditary angioedema (HAE), genetic mutations result in deficient or dysfunctional C1-INH and dysregulation of the contact system leading to recurrent, sometimes fatal, angioedema attacks. IONIS-PKKRx is a second-generation 2′-O-(2-methoxyethyl)-modified chimeric antisense oligonucleotide, designed to bind and selectively reduce prekallikrein (PKK) mRNA in the liver. IONIS-PKKRx demonstrated dose-dependent reduction of human prekallikrein hepatic mRNA and plasma protein in transgenic mice and dose- and time-dependent reductions of plasma PKK in Cynomolgus monkeys. Similar dose-dependent reductions of plasma PKK levels were observed in healthy human volunteers accompanied by decreases in bradykinin generation capacity with an acceptable safety and tolerability profile. These results highlight a novel and specific approach to target PKK for the treatment of HAE and other diseases involving contact system activation and overproduction of bradykinin.
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