期刊文献+

固有免疫细胞代谢重编程调控脓毒症免疫稳态的研究进展 被引量:10

Research progress on metabolic reprogramming of innate immune cells involved in immune-regulation of sepsis
原文传递
导出
摘要 免疫抑制引起脓毒症后期死亡风险增加.中性粒细胞、单核/巨噬细胞、自然杀伤细胞(NK细胞)和树突细胞等固有免疫细胞功能失调与脓毒症免疫抑制有关.近年来,免疫细胞代谢重编程是研究脓毒症免疫调节的热点问题.本文以固有免疫细胞为切入点,分析总结中性粒细胞脂肪酸合成代谢、单核/巨噬细胞葡萄糖和精氨酸代谢、NK细胞"驯化"与糖酵解、糖脂代谢、线粒体合成以及树突细胞分化、成熟、活化进行综述,以期深入理解脓毒症免疫代谢调节机制. Immunosuppression plays a critical role in death of sepsis. Innate immunity is the first line defense to prevent pathogen invasion, and neutrophils, macrophages, dendritic cells and natural killer cells (NK cells) are closely involved in the process of the immune-regulation during sepsis. Recently, metabolic reprogramming in immune cells is known as a keystone for immune intervention therapy in sepsis. Here, we focus on the recent advances in metabolic regulation in neutrophils, macrophages, dendritic cells and NK cells including glycolysis, fatty acid synthesis, fatty acid oxidation and arginine metabolism involved in the immune-regulation of sepsis. This review will be helpful to summarize the mechanisms underlying sepsis-induced immunosuppression.
作者 邵卢晶 王春霞 张育才 Shao Lujing;Wang Chunxia;Zhang Yucai(Department of Critical Care Medicine,Shanghai Children's Hospital,Shanghai Jiao Tong University,Institute of Pediatric Critical Care,Shanghai Jiao Tong University,Shanghai 200062,China)
出处 《中华危重病急救医学》 CAS CSCD 北大核心 2019年第7期910-912,共3页 Chinese Critical Care Medicine
基金 上海市科委科技创新行动计划项目(18411951000).
关键词 脓毒症 固有免疫 代谢重编程 免疫抑制 Sepsis Innate immunity Metabolic reprogramming Immunosuppression
  • 相关文献

参考文献2

二级参考文献135

  • 1Barth E,Fischer G,Schneider E M,et al.Differences in the expression of CD64 and CD14 (mCD14) on polymorphonuclear cells and on monocytes in patients with septic shock [J]. Cytokine, 2001,14: 299 -302.
  • 2Saccani S, Saccani S, Varesio, et al.Divergent effects of dithiocarbamates onAP-l-containing and AP - 1 - less NFAT sites [J]. Eur J Immunol, 1999,29:1194 - 1201.
  • 3Angus D C,Linde -Zwirble W T,Lidicker J,et al. Epidemiology of severe sepsis in the United States:analysis of incidence,outcome, and associated costs of care [J].Crit Care Med,2001,29:1303 - 1310.
  • 4Arbour N C,Lorenz E,Schutte B C,et al.TLR4 mutations are associated with endotoxin hyporesponsiveness in human [J].Nat Genet,2000,25:187 - 191.
  • 5Oberholzer A,Oberholzer C,Moldawer L L, et al. Sepsis syndromes: understanding the role of innate and acquired immunity [J]. Shock,2001,16:83 - 96.
  • 6Pellegrini J D,De A K,Kodys K,et al.Relationships between T lymphocyte apoptosis and anergy following trauma [J]. J Surg Res, 2000,88: 200 - 206.
  • 7Hotchkiss R S,Swanson P E,Freeman B D, et al. Apoptotic cell death in patients with sepsis, shock and multiple organ dysfunction[J]. Crit Care Med, 1999,27 :1230 - 1251.
  • 8Li X C,Wells A D,Strom T B,et al. The role of T cell apoptosis in transplantation tolerance [J]. Curt Opin Immunol, 2000,12:522 - 527.
  • 9Green D R, Beere H M. Apoptosis: gone but not forgotten [J]. Nature, 2000,405:28 - 29.
  • 10Hotchkiss R S,Tinsley K W,Swanson P E,et al. Depletion of dendritic cells, but not macrophages, in patients with sepsis [J]. J Immunol, 2002,168: 2493 - 2500.

共引文献141

同被引文献58

引证文献10

二级引证文献36

相关作者

内容加载中请稍等...

相关机构

内容加载中请稍等...

相关主题

内容加载中请稍等...

浏览历史

内容加载中请稍等...
;
使用帮助 返回顶部