Autor: |
Koide, Hiroyuki, Okishima, Anna, Hoshino, Yu, Kamon, Yuri, Yoshimatsu, Keiichi, Saito, Kazuhiro, Yamauchi, Ikumi, Ariizumi, Saki, Zhou, Yuqi, Xiao, Ting-Hui, Goda, Keisuke, Oku, Naoto, Asai, Tomohiro, Shea, Kenneth J. |
Předmět: |
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Zdroj: |
Nature Communications; 9/21/2021, Vol. 12 Issue 1, p1-14, 14p |
Abstrakt: |
Sepsis is a life-threatening condition caused by the extreme release of inflammatory mediators into the blood in response to infection (e.g., bacterial infection, COVID-19), resulting in the dysfunction of multiple organs. Currently, there is no direct treatment for sepsis. Here we report an abiotic hydrogel nanoparticle (HNP) as a potential therapeutic agent for late-stage sepsis. The HNP captures and neutralizes all variants of histones, a major inflammatory mediator released during sepsis. The highly optimized HNP has high capacity and long-term circulation capability for the selective sequestration and neutralization of histones. Intravenous injection of the HNP protects mice against a lethal dose of histones through the inhibition of platelet aggregation and migration into the lungs. In vivo administration in murine sepsis model mice results in near complete survival. These results establish the potential for synthetic, nonbiological polymer hydrogel sequestrants as a new intervention strategy for sepsis therapy and adds to our understanding of the importance of histones to this condition. Sepsis caused by the release of inflammatory mediators into the blood is a life threatening disease. Here, the authors report on the development of hydrogel nanoparticles for the capture and neutralisation of histones, major inflammatory mediators, and demonstrate sepsis treatment in a murine model. [ABSTRACT FROM AUTHOR] |
Databáze: |
Complementary Index |
Externí odkaz: |
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