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一种针对多重耐药革兰氏阴性菌感染的宿主导向型大环肽治疗药物。

A host-directed macrocyclic peptide therapeutic for MDR gram negative bacterial infections.

机构信息

Department of Pathology and Laboratory Medicine, Keck School of Medicine, University of Southern California, Los Angeles, CA, USA.

Department of Clinical Immunology and Rheumatology/Infectious Disease, Kyushu University Hospital, Fukuoka, Japan.

出版信息

Sci Rep. 2021 Dec 6;11(1):23447. doi: 10.1038/s41598-021-02619-y.

Abstract

The emergence of infections by carbapenem resistant Enterobacteriaceae (CRE) pathogens has created an urgent public health threat, as carbapenems are among the drugs of last resort for infections caused by a growing fraction of multi-drug resistant (MDR) bacteria. There is global consensus that new preventive and therapeutic strategies are urgently needed to combat the growing problem of MDR bacterial infections. Here, we report on the efficacy of a novel macrocyclic peptide, minimized theta-defensin (MTD)-12813 in CRE sepsis. MTD12813 is a theta-defensin inspired cyclic peptide that is highly effective against CRE pathogens K. pneumoniae and E. coli in vivo. In mouse septicemia models, single dose administration of MTD12813 significantly enhanced survival by promoting rapid host-mediated bacterial clearance and by modulating pathologic cytokine responses, restoring immune homeostasis, and preventing lethal septic shock. The peptide lacks direct antibacterial activity in the presence of mouse serum or in peritoneal fluid, further evidence for its indirect antibacterial mode of action. MTD12813 is highly stable in biological matrices, resistant to bacterial proteases, and nontoxic to mice at dose levels 100 times the therapeutic dose level, properties which support further development of the peptide as a first in class anti-infective therapeutic.

摘要

碳青霉烯类耐药肠杆菌科(CRE)病原体感染的出现带来了紧迫的公共卫生威胁,因为碳青霉烯类药物是治疗越来越多的多药耐药(MDR)细菌感染的最后手段之一。全球一致认为,迫切需要新的预防和治疗策略来应对日益严重的 MDR 细菌感染问题。在这里,我们报告了新型大环肽,最小化θ-防御素(MTD)-12813 对 CRE 败血症的疗效。MTD12813 是一种基于θ-防御素的环状肽,对 CRE 病原体肺炎克雷伯菌和大肠杆菌具有高度的体内活性。在小鼠败血性休克模型中,单次给予 MTD12813 可显著提高存活率,促进快速的宿主介导的细菌清除,并通过调节病理性细胞因子反应,恢复免疫稳态,防止致命性休克。该肽在有或无鼠血清或腹腔液存在时均无直接的抗菌活性,进一步证明了其间接的抗菌作用模式。MTD12813 在生物基质中高度稳定,对细菌蛋白酶具有抗性,在治疗剂量水平的 100 倍剂量下对小鼠无毒,这些特性支持该肽作为一种新型抗感染治疗药物的进一步开发。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/9555/8648872/9c4fe6df770d/41598_2021_2619_Fig1_HTML.jpg

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