-1β,

N A Thornberry1, H G Bull, J R Calaycay

  • 1Department of Biochemistry, Merck Research Laboratories, Rahway, New Jersey 07065.

Nature
|April 30, 1992
PubMed
まとめ

研究者は,インタールイキン-1β (IL-1β) 変換酵素,システインプロテアゼ,および設計された阻害剤を特定しました. モノサイトにおけるこの酵素を阻害すると,成熟したIL-1βの産生が停止し,炎症の治療標的として示唆される.

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