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KMRC011,一种 Toll 样受体 5 的激动剂,可减轻食蟹猴的辐照诱导的组织损伤和死亡率。

KMRC011, an agonist of toll-like receptor 5, mitigates irradiation-induced tissue damage and mortality in cynomolgus monkeys.

机构信息

Jeonbuk Department of Inhalation Research, Korea Institute of Toxicology, Jeongeup-si, Republic of Korea.

Deptartment of Advanced Toxicology Research, Korea Institute of Toxicology, Daejeon-si, Republic of Korea.

出版信息

J Immunotoxicol. 2020 Dec;17(1):31-42. doi: 10.1080/1547691X.2019.1699617.

DOI:10.1080/1547691X.2019.1699617
PMID:32013650
Abstract

In the study here, the potential applicability of KMRC011 - an agonist of toll-like receptor-5 - as a countermeasure for radiation toxicities was evaluated. Following a single 5.5 Gy total body irradiation (TBI, surface absorbed dose = 7 Gy) of Co γ-rays, mortality rates and degrees of pathological lesions that developed over 80 days were compared in monkeys that received TBI only and a group that was injected once with KMRC011 (10 μg/kg) after TBI. Compared to the TBI-only hosts (80%), the death rate was significantly improved by the use of KMRC011 (40%), all deaths in both groups occurred in the period from Days 19-24 post-TBI. Further analysis of monkeys that survived until the end of the experiment showed that AST and ALT levels were elevated only in the TBI group, and that radiation-induced tissue damage was alleviated by the KMRC011 injection. Additionally, expression of cell death-related proteins was lower in tissues from the KMRC011-treated hosts than in those in the TBI-only group. Other measured parameters, including body weight, food uptake, and hematological values did not significantly differ between the two groups over the entire period. The results of this study, thus demonstrate that KMRC011 could potentially be used as a medical countermeasure for the treatment of acute radiation exposure.

摘要

在本研究中,评估了 KMRC011(一种 Toll 样受体 5 的激动剂)作为辐射毒性对策的潜在适用性。在 Co γ射线单次 5.5Gy 全身照射(TBI,表面吸收剂量=7Gy)后,比较了仅接受 TBI 的猴子和接受 TBI 后单次注射 KMRC011(10μg/kg)的猴子在 80 天内的死亡率和病理损伤程度。与仅接受 TBI 的宿主(80%)相比,KMRC011 的使用显著提高了死亡率(40%),两组的所有死亡均发生在 TBI 后第 19-24 天。对幸存至实验结束的猴子进行的进一步分析表明,AST 和 ALT 水平仅在 TBI 组升高,并且 KMRC011 注射减轻了辐射引起的组织损伤。此外,与仅接受 TBI 的组相比,KMRC011 处理的宿主组织中与细胞死亡相关的蛋白表达水平较低。在整个研究期间,两组的其他测量参数,包括体重、食物摄取量和血液学值均无显著差异。因此,这项研究的结果表明,KMRC011 可能可作为治疗急性辐射暴露的医疗对策。

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