TY - JOUR
T1 - Synthetic hydrogel nanoparticles for sepsis therapy
AU - Koide, Hiroyuki
AU - Okishima, Anna
AU - Hoshino, Yu
AU - Kamon, Yuri
AU - Yoshimatsu, Keiichi
AU - Saito, Kazuhiro
AU - Yamauchi, Ikumi
AU - Ariizumi, Saki
AU - Zhou, Yuqi
AU - Xiao, Ting Hui
AU - Goda, Keisuke
AU - Oku, Naoto
AU - Asai, Tomohiro
AU - Shea, Kenneth J.
N1 - Funding Information:
This work was supported by JSPS KAKENHI Grant Numbers JP19H04450. This work is partly supported by JSPS Core-to-Core Program and White Rock Foundation. We thank T. Ozeki for their help with QCM measurements.
Publisher Copyright:
© 2021, The Author(s).
PY - 2021/12/1
Y1 - 2021/12/1
N2 - 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.
AB - 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.
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U2 - 10.1038/s41467-021-25847-2
DO - 10.1038/s41467-021-25847-2
M3 - Article
C2 - 34548486
AN - SCOPUS:85115438247
VL - 12
JO - Nature Communications
JF - Nature Communications
SN - 2041-1723
IS - 1
M1 - 5552
ER -