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TLR5 激动剂恩利莫德减少了 TNF 的不良反应毒性,同时保留了其抗肿瘤作用。

TLR5 agonist entolimod reduces the adverse toxicity of TNF while preserving its antitumor effects.

机构信息

Department of Cell Stress Biology, Roswell Park Comprehensive Cancer Center, Buffalo, New York, United States America.

Genome Protection, Inc., Buffalo, New York, United States of America.

出版信息

PLoS One. 2020 Feb 6;15(2):e0227940. doi: 10.1371/journal.pone.0227940. eCollection 2020.

Abstract

Tumor necrosis factor alpha (TNF) is capable of inducing regression of solid tumors. However, TNF released in response to Toll-like receptor 4 (TLR4) activation by bacterial lipopolysaccharide (LPS) is the key mediator of cytokine storm and septic shock that can cause severe tissue damage limiting anticancer applications of this cytokine. In our previous studies, we demonstrated that activation of another Toll-like receptor, TLR5, could protect from tissue damage caused by a variety of stresses including radiation, chemotherapy, Fas-activating antibody and ischemia-reperfusion. In this study, we tested whether entolimod could counteract TNF-induced toxicity in mouse models. We found that entolimod pretreatment effectively protects livers and lungs from LPS- and TNF-induced toxicity and prevents mortality caused by combining either of these agents with the sensitizer, D-galactosamine. While LPS and TNF induced significant activation of apoptotic caspase 3/7, lipid tissue peroxidation and serum ALT accumulation in mice without entolimod treatment, these indicators of toxicity were reduced by entolimod pretreatment to the levels of untreated control mice. Entolimod was effective when injected 0.5-48 hours prior to, but not when injected simultaneously or after LPS or TNF. Using chimeric mice with hematopoiesis differing in its TLR5 status from the rest of tissues, we showed that this protective activity was dependent on TLR5 expression by non-hematopoietic cells. Gene expression analysis identified multiple genes upregulated by entolimod in the liver and cultured hepatocytes as possible mediators of its protective activity. Entolimod did not interfere with the antitumor activity of TNF in mouse hepatocellular and colorectal tumor models. These results support further development of TLR5 agonists to increase tissue resistance to cytotoxic cytokines, reduce the risk of septic shock and enable safe systemic application of TNF as an anticancer therapy.

摘要

肿瘤坏死因子-α(TNF)能够诱导实体瘤消退。然而,细菌脂多糖(LPS)激活 Toll 样受体 4(TLR4)后释放的 TNF 是细胞因子风暴和脓毒症休克的关键介质,可导致严重的组织损伤,限制了该细胞因子的抗癌应用。在我们之前的研究中,我们证明了另一种 Toll 样受体 TLR5 的激活可以保护组织免受各种应激(包括辐射、化疗、Fas 激活抗体和缺血再灌注)引起的损伤。在这项研究中,我们测试了恩替莫德是否可以对抗 TNF 诱导的小鼠模型中的毒性。我们发现,恩替莫德预处理可有效保护肝脏和肺部免受 LPS 和 TNF 诱导的毒性,并防止将这些药物中的任何一种与敏化剂 D-半乳糖胺结合使用引起的死亡率。虽然 LPS 和 TNF 在没有恩替莫德治疗的情况下可显著激活凋亡 Caspase 3/7、脂质组织过氧化和血清 ALT 积累,但这些毒性指标在恩替莫德预处理后降低至未处理对照小鼠的水平。恩替莫德在 LPS 或 TNF 注射前 0.5-48 小时内有效,但在同时或之后注射无效。使用造血组织 TLR5 状态与其他组织不同的嵌合小鼠,我们表明这种保护活性依赖于非造血细胞 TLR5 的表达。基因表达分析确定了恩替莫德在肝脏和培养的肝细胞中上调的多个基因,这些基因可能是其保护活性的介导物。恩替莫德不干扰 TNF 在小鼠肝细胞和结直肠肿瘤模型中的抗肿瘤活性。这些结果支持进一步开发 TLR5 激动剂以增加组织对细胞毒性细胞因子的抵抗力,降低脓毒症休克的风险,并使 TNF 作为抗癌疗法的安全全身应用成为可能。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/10be/7004342/755426878bd8/pone.0227940.g001.jpg

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