• 文献检索
  • 文档翻译
  • 深度研究
  • 学术资讯
  • Suppr Zotero 插件Zotero 插件
  • 邀请有礼
  • 套餐&价格
  • 历史记录
应用&插件
Suppr Zotero 插件Zotero 插件浏览器插件Mac 客户端Windows 客户端微信小程序
定价
高级版会员购买积分包购买API积分包
服务
文献检索文档翻译深度研究API 文档MCP 服务
关于我们
关于 Suppr公司介绍联系我们用户协议隐私条款
关注我们

Suppr 超能文献

核心技术专利:CN118964589B侵权必究
粤ICP备2023148730 号-1Suppr @ 2026

文献检索

告别复杂PubMed语法,用中文像聊天一样搜索,搜遍4000万医学文献。AI智能推荐,让科研检索更轻松。

立即免费搜索

文件翻译

保留排版,准确专业,支持PDF/Word/PPT等文件格式,支持 12+语言互译。

免费翻译文档

深度研究

AI帮你快速写综述,25分钟生成高质量综述,智能提取关键信息,辅助科研写作。

立即免费体验

大分子在防治脓毒症中的研究进展。

Research Progress of Macromolecules in the Prevention and Treatment of Sepsis.

机构信息

Fujian Key Laboratory of Innate Immune Biology, Biomedical Research Center of South China, College of Life Science, Fujian Normal University, Fuzhou 350117, China.

出版信息

Int J Mol Sci. 2023 Aug 21;24(16):13017. doi: 10.3390/ijms241613017.

DOI:10.3390/ijms241613017
PMID:37629199
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC10455590/
Abstract

Sepsis is associated with high rates of mortality in the intensive care unit and accompanied by systemic inflammatory reactions, secondary infections, and multiple organ failure. Biological macromolecules are drugs produced using modern biotechnology to prevent or treat diseases. Indeed, antithrombin, antimicrobial peptides, interleukins, antibodies, nucleic acids, and lentinan have been used to prevent and treat sepsis. In vitro, biological macromolecules can significantly ameliorate the inflammatory response, apoptosis, and multiple organ failure caused by sepsis. Several biological macromolecules have entered clinical trials. This review summarizes the sources, efficacy, mechanism of action, and research progress of macromolecular drugs used in the prevention and treatment of sepsis.

摘要

脓毒症与重症监护病房(ICU)高死亡率相关,并伴有全身炎症反应、继发感染和多器官衰竭。生物大分子是使用现代生物技术生产的药物,用于预防或治疗疾病。事实上,已使用抗凝血酶、抗菌肽、白细胞介素、抗体、核酸和香菇多糖来预防和治疗脓毒症。在体外,生物大分子可显著改善脓毒症引起的炎症反应、细胞凋亡和多器官衰竭。几种生物大分子已进入临床试验阶段。本文总结了用于脓毒症预防和治疗的生物大分子药物的来源、疗效、作用机制和研究进展。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/12e9/10455590/979b33beb56c/ijms-24-13017-g008.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/12e9/10455590/8148591f2027/ijms-24-13017-g001.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/12e9/10455590/ac1ba2722b37/ijms-24-13017-g002.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/12e9/10455590/18bece989c9c/ijms-24-13017-g003.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/12e9/10455590/846be873b6e4/ijms-24-13017-g004.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/12e9/10455590/40efb15c776e/ijms-24-13017-g005.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/12e9/10455590/201a91738070/ijms-24-13017-g006.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/12e9/10455590/811b8ca349b1/ijms-24-13017-g007.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/12e9/10455590/979b33beb56c/ijms-24-13017-g008.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/12e9/10455590/8148591f2027/ijms-24-13017-g001.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/12e9/10455590/ac1ba2722b37/ijms-24-13017-g002.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/12e9/10455590/18bece989c9c/ijms-24-13017-g003.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/12e9/10455590/846be873b6e4/ijms-24-13017-g004.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/12e9/10455590/40efb15c776e/ijms-24-13017-g005.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/12e9/10455590/201a91738070/ijms-24-13017-g006.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/12e9/10455590/811b8ca349b1/ijms-24-13017-g007.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/12e9/10455590/979b33beb56c/ijms-24-13017-g008.jpg

相似文献

1
Research Progress of Macromolecules in the Prevention and Treatment of Sepsis.大分子在防治脓毒症中的研究进展。
Int J Mol Sci. 2023 Aug 21;24(16):13017. doi: 10.3390/ijms241613017.
2
Antithrombin III in patients with severe sepsis. A randomized, placebo-controlled, double-blind multicenter trial plus a meta-analysis on all randomized, placebo-controlled, double-blind trials with antithrombin III in severe sepsis.严重脓毒症患者的抗凝血酶III。一项随机、安慰剂对照、双盲多中心试验以及对所有使用抗凝血酶III治疗严重脓毒症的随机、安慰剂对照、双盲试验的荟萃分析。
Intensive Care Med. 1998 Jul;24(7):663-72. doi: 10.1007/s001340050642.
3
Sepsis and organ dysfunction/failure. An overview.脓毒症与器官功能障碍/衰竭。概述
Minerva Anestesiol. 1999 Jul-Aug;65(7-8):529-40.
4
Caring for the critically ill patient. High-dose antithrombin III in severe sepsis: a randomized controlled trial.重症患者的护理。严重脓毒症中高剂量抗凝血酶III:一项随机对照试验。
JAMA. 2001 Oct 17;286(15):1869-78. doi: 10.1001/jama.286.15.1869.
5
Human protein C zymogen concentrate in patients with severe sepsis and multiple organ failure after adult cardiac surgery.成人心脏手术后严重脓毒症和多器官衰竭患者的人蛋白 C 酶原浓缩物。
Intensive Care Med. 2009 Nov;35(11):1959-63. doi: 10.1007/s00134-009-1584-3. Epub 2009 Aug 1.
6
Pathogenesis of Multiple Organ Failure in Sepsis.脓毒症中多器官功能衰竭的发病机制
Crit Rev Immunol. 2015;35(4):277-91. doi: 10.1615/critrevimmunol.2015015461.
7
Do statins have a role in preventing or treating sepsis?他汀类药物在预防或治疗败血症方面有作用吗?
Crit Care. 2006 Feb;10(1):113. doi: 10.1186/cc3972.
8
Research Progress on Natural Small-Molecule Compounds for the Prevention and Treatment of Sepsis.天然小分子化合物防治脓毒症的研究进展。
Int J Mol Sci. 2023 Aug 12;24(16):12732. doi: 10.3390/ijms241612732.
9
Microcirculatory disorders in sepsis and transplantation: therapy with natural coagulatory inhibitors antithrombin and activated protein C.脓毒症和移植中的微循环障碍:天然凝血抑制剂抗凝血酶和活化蛋白C的治疗作用
Curr Opin Crit Care. 2006 Oct;12(5):426-30. doi: 10.1097/01.ccx.0000244121.54495.f7.
10
Role of the tissue factor pathway in the pathogenesis and management of multiple organ failure.组织因子途径在多器官功能衰竭发病机制及治疗中的作用
Blood Coagul Fibrinolysis. 2004 May;15 Suppl 1:S11-20. doi: 10.1097/00001721-200405001-00003.

引用本文的文献

1
LncRNA DLEU1 contributes to the progression of septic myocardial dysfunction by targeting miR-381-3p.长链非编码RNA DLEU1通过靶向miR-381-3p促进脓毒症性心肌功能障碍的进展。
Cent Eur J Immunol. 2024;49(3):227-237. doi: 10.5114/ceji.2024.144199. Epub 2024 Nov 12.
2
Administration of turmeric kombucha ameliorates lipopolysaccharide-induced sepsis by attenuating inflammation and modulating gut microbiota.给予姜黄康普茶可通过减轻炎症和调节肠道微生物群来改善脂多糖诱导的败血症。
Front Microbiol. 2024 Aug 30;15:1452190. doi: 10.3389/fmicb.2024.1452190. eCollection 2024.
3
Inhibitory mechanisms of decoy receptor 3 in cecal ligation and puncture-induced sepsis.

本文引用的文献

1
Solidification and oral delivery of biologics to the colon- A review.生物制剂的结肠固化和口服递药 - 综述。
Eur J Pharm Sci. 2023 Nov 1;190:106523. doi: 10.1016/j.ejps.2023.106523. Epub 2023 Jul 8.
2
Effectiveness of early heparin therapy on outcomes in critically ill patients with sepsis-induced coagulopathy.早期肝素治疗对脓毒症诱导的凝血病重症患者预后的有效性。
Front Pharmacol. 2023 May 15;14:1173893. doi: 10.3389/fphar.2023.1173893. eCollection 2023.
3
Intravenously administered interleukin-7 to reverse lymphopenia in patients with septic shock: a double-blind, randomized, placebo-controlled trial.
诱饵受体 3 在盲肠结扎和穿刺诱导脓毒症中的抑制机制。
mBio. 2024 Jun 12;15(6):e0052124. doi: 10.1128/mbio.00521-24. Epub 2024 May 3.
静脉注射白细胞介素-7逆转感染性休克患者淋巴细胞减少症:一项双盲、随机、安慰剂对照试验。
Ann Intensive Care. 2023 Mar 12;13(1):17. doi: 10.1186/s13613-023-01109-w.
4
Tocilizumab attenuates acute lung injury in rats with sepsis by regulating S100A12/NLRP3.托珠单抗通过调节S100A12/NLRP3减轻脓毒症大鼠的急性肺损伤。
Am J Transl Res. 2023 Jan 15;15(1):99-113. eCollection 2023.
5
Fibroblast growth factor 2 (FGF2) ameliorates the coagulation abnormalities in sepsis.成纤维细胞生长因子 2(FGF2)可改善脓毒症的凝血异常。
Toxicol Appl Pharmacol. 2023 Feb 1;460:116364. doi: 10.1016/j.taap.2023.116364. Epub 2023 Jan 6.
6
Beneficial effects of tannic acid on comorbid anxiety in cecal ligation and puncture-induced sepsis in rats and potential underlying mechanisms.鞣酸对大鼠盲肠结扎和穿刺诱导的脓毒症共病焦虑的有益作用及潜在机制
Naunyn Schmiedebergs Arch Pharmacol. 2023 May;396(5):1019-1030. doi: 10.1007/s00210-022-02374-5. Epub 2023 Jan 4.
7
Growth Differentiation Factor 7 Prevents Sepsis-Induced Acute Lung Injury in Mice.生长分化因子7可预防小鼠脓毒症诱导的急性肺损伤。
Evid Based Complement Alternat Med. 2022 Dec 22;2022:3676444. doi: 10.1155/2022/3676444. eCollection 2022.
8
Association between different concentrations of human serum albumin and 28-day mortality in intensive care patients with sepsis: A propensity score matching analysis.不同浓度人血清白蛋白与脓毒症重症监护患者28天死亡率之间的关联:一项倾向评分匹配分析
Front Pharmacol. 2022 Dec 12;13:1037893. doi: 10.3389/fphar.2022.1037893. eCollection 2022.
9
Toxicological and Safety Pharmacological Profiling of the Anti-Infective and Anti-Inflammatory Peptide Pep19-2.5.抗感染及抗炎肽Pep19-2.5的毒理学和安全药理学分析
Microorganisms. 2022 Dec 6;10(12):2412. doi: 10.3390/microorganisms10122412.
10
Antifungal and Anti-Inflammatory Activities of PS1-2 Peptide against Fluconazole-Resistant .PS1-2肽对氟康唑耐药菌的抗真菌和抗炎活性
Antibiotics (Basel). 2022 Dec 8;11(12):1779. doi: 10.3390/antibiotics11121779.