留言板

尊敬的读者、作者、审稿人, 关于本刊的投稿、审稿、编辑和出版的任何问题, 您可以本页添加留言。我们将尽快给您答复。谢谢您的支持!

姓名
邮箱
手机号码
标题
留言内容
验证码

补体系统激活在烧伤后免疫中的作用研究进展

黄圣宇 朱峰 郭光华

黄圣宇, 朱峰, 郭光华. 补体系统激活在烧伤后免疫中的作用研究进展[J]. 中华烧伤与创面修复杂志, 2023, 39(4): 396-400. DOI: 10.3760/cma.j.cn501225-20220726-00313.
引用本文: 黄圣宇, 朱峰, 郭光华. 补体系统激活在烧伤后免疫中的作用研究进展[J]. 中华烧伤与创面修复杂志, 2023, 39(4): 396-400. DOI: 10.3760/cma.j.cn501225-20220726-00313.
Huang SY,Zhu F,Guo GH.Research advances on the role of complement system activation in post-burn immunity[J].Chin J Burns Wounds,2023,39(4):396-400.DOI: 10.3760/cma.j.cn501225-20220726-00313.
Citation: Huang SY,Zhu F,Guo GH.Research advances on the role of complement system activation in post-burn immunity[J].Chin J Burns Wounds,2023,39(4):396-400.DOI: 10.3760/cma.j.cn501225-20220726-00313.

补体系统激活在烧伤后免疫中的作用研究进展

doi: 10.3760/cma.j.cn501225-20220726-00313
基金项目: 

国家重点研发计划 2019YFA0110601

国家自然科学基金地区科学基金项目 82160376, 81760342, 81960352

江西省科技厅重点研发计划重点项目 20171ACG70004

江西省青年科学基金项目 20192BAB215029

详细信息
    通讯作者:

    郭光华,Email:guogh2000@hotmail.com

Research advances on the role of complement system activation in post-burn immunity

Funds: 

National Key Research and Development Program of China 2019YFA0110601

Regional Science Foundation Program of National Natural Science Foundation of China 82160376, 81760342, 81960352

Key Program for Key Research and Development Program of Science and Technology Department of Jiangxi Province of China 20171ACG70004

Youth Science Fund Project of Jiangxi Province of China 20192BAB215029

More Information
  • 摘要: 免疫激活是烧伤后继发性损伤的重要因素之一,也是抗感染过程中主要的机体反应。补体系统作为先天性免疫反应中的重要部分,能够在烧伤后诱导免疫细胞激活,促进炎症与介导免疫屏障的破坏,甚至与凝血级联发生复杂交联。该文从先天性免疫、获得性免疫以及补体系统与凝血级联交联的角度,综述补体系统激活在烧伤后免疫中的作用及其在临床中转化的可能性。

     

  • 参考文献(46)

    [1] MannesM,SchmidtCQ,NilssonB,et al.Complement as driver of systemic inflammation and organ failure in trauma, burn, and sepsis[J].Semin Immunopathol,2021,43(6):773-788.DOI: 10.1007/s00281-021-00872-x.
    [2] SierawskaO,MałkowskaP,TaskinC,et al.Innate immune system response to burn damage-focus on cytokine alteration[J].Int J Mol Sci,2022,23(2):716.DOI: 10.3390/ijms23020716.
    [3] PeckCT,StraußS,StahlGL,et al.Mannose-binding lectin (MBL) and the lectin complement pathway play a role in cutaneous ischemia and reperfusion injury[J].Innov Surg Sci,2020,5(1/2):43-51.DOI:1 0.1515/iss-2020-0017.
    [4] KorkmazHI,UlrichMMW,van WieringenWN,et al.The local and systemic inflammatory response in a pig burn wound model with a pivotal role for complement[J].J Burn Care Res,2017,38(5):e796-e806.DOI: 10.1097/BCR.0000000000000486.
    [5] Afshar-KharghanV.The role of the complement system in cancer[J].J Clin Invest,2017,127(3):780-789.DOI: 10.1172/JCI90962.
    [6] MorganM,DeuisJR,WoodruffTM,et al.Role of complement anaphylatoxin receptors in a mouse model of acute burn-induced pain[J].Mol Immunol,2018,94:68-74.DOI: 10.1016/j.molimm.2017.12.016.
    [7] LaggnerM,LingitzMT,CopicD,et al.Severity of thermal burn injury is associated with systemic neutrophil activation[J].Sci Rep,2022,12(1):1654.DOI: 10.1038/s41598-022-05768-w.
    [8] ComishPB,CarlsonD,KangR,et al.Damage-associated molecular patterns and the systemic immune consequences of severe thermal injury[J].J Immunol,2020,205(5):1189-1197.DOI: 10.4049/jimmunol.2000439.
    [9] SatyamA,GraefER,LapchakPH,et al.Complement and coagulation cascades in trauma[J].Acute Med Surg,2019,6(4):329-335.DOI: 10.1002/ams2.426.
    [10] PadfieldKE,ZhangQ,GopalanS,et al.Local and distant burn injury alter immuno-inflammatory gene expression in skeletal muscle[J].J Trauma,2006,61(2):280-292.DOI: 10.1097/01.ta.0000230567.56797.6c.
    [11] RadkeA,MottaghyK,GoldmannC,et al.C1 inhibitor prevents capillary leakage after thermal trauma[J].Crit Care Med,2000,28(9):3224-3232.DOI: 10.1097/00003246-200009000-00018.
    [12] SadeghipourH,TorabiR,GottschallJ,et al.Blockade of IgM-mediated inflammation alters wound progression in a swine model of partial-thickness burn[J].J Burn Care Res,2017,38(3):148-160.DOI: 10.1097/BCR.0000000000000459.
    [13] WuM,RoweJM,FlemingSD.Complement initiation varies by sex in intestinal ischemia reperfusion injury[J].Front Immunol,2021,12:649882.DOI: 10.3389/fimmu.2021.649882.
    [14] 贺伟峰,罗高兴.皮肤免疫在创面愈合中的作用[J].中华烧伤杂志,2020,36(10):901-904.DOI: 10.3760/cma.j.cn501120-20200823-00389.
    [15] BegienemanMP,KubatB,UlrichMM,et al.Prolonged C1 inhibitor administration improves local healing of burn wounds and reduces myocardial inflammation in a rat burn wound model[J].J Burn Care Res,2012,33(4):544-551.DOI: 10.1097/BCR.0b013e31823bc2fc.
    [16] Khorram-SefatR,GoldmannC,RadkeA,et al.The therapeutic effect of C1-inhibitor on gut-derived bacterial translocation after thermal injury[J].Shock,1998,9(2):101-108.DOI: 10.1097/00024382-199802000-00005.
    [17] MulliganMS,YehCG,RudolphAR,et al.Protective effects of soluble CR1 in complement- and neutrophil-mediated tissue injury[J].J Immunol,1992,148(5):1479-1485.
    [18] KorkmazHI,UlrichMMW,WieringenWNV,et al.C1 inhibitor administration reduces local inflammation and capillary leakage, without affecting long-term wound healing parameters, in a pig burn wound model[J].Antiinflamm Antiallergy Agents Med Chem,2021,20(2):150-160.DOI: 10.2174/1871523019666200702101513.
    [19] SuberF,CarrollMC,MooreFDJr.Innate response to self-antigen significantly exacerbates burn wound depth[J].Proc Natl Acad Sci U S A,2007,104(10):3973-3977.DOI: 10.1073/pnas.0609026104.
    [20] ZhengD,LiwinskiT,ElinavE.Interaction between microbiota and immunity in health and disease[J].Cell Res,2020,30(6):492-506.DOI: 10.1038/s41422-020-0332-7.
    [21] ZhengQY,XuF,YangY,et al.C5a/C5aR1 mediates IMQ-induced psoriasiform skin inflammation by promoting IL-17A production from γδ-T cells[J].FASEB J,2020,34(8):10590-10604.DOI: 10.1096/fj.202000384R.
    [22] SchmidE,PiccoloMT,FriedlHP,et al.Requirement for C5a in lung vascular injury following thermal trauma to rat skin[J].Shock,1997,8(2):119-124.DOI: 10.1097/00024382-199708000-00010.
    [23] LuckME,HerrnreiterCJ,ChoudhryMA.Gut microbial changes and their contribution to post-burn pathology[J].Shock,2021,56(3):329-344.DOI: 10.1097/SHK.0000000000001736.
    [24] VindenesH,BjerknesR.Activation of polymorphonuclear neutrophilic granulocytes following burn injury: alteration of Fc-receptor and complement-receptor expression and of opsonophagocytosis[J].J Trauma,1994,36(2):161-167.DOI: 10.1097/00005373-199402000-00001.
    [25] DeitchEA,LuQ,XuDZ,et al.Effect of local and systemic burn microenvironment on neutrophil activation as assessed by complement receptor expression and morphology[J].J Trauma,1990,30(3):259-268.DOI: 10.1097/00005373-199003000-00003.
    [26] ZuoY,KanthiY,KnightJS,et al.The interplay between neutrophils, complement, and microthrombi in COVID-19[J].Best Pract Res Clin Rheumatol,2021,35(1):101661.DOI: 10.1016/j.berh.2021.101661.
    [27] ChenZ,ZhangH,QuM,et al.Review: the emerging role of neutrophil extracellular traps in sepsis and sepsis-associated thrombosis[J].Front Cell Infect Microbiol,2021,11:653228.DOI: 10.3389/fcimb.2021.653228.
    [28] Delvasto-NuñezL,JongeriusI,ZeerlederS.It takes two to thrombosis: hemolysis and complement[J].Blood Rev,2021,50:100834.DOI: 10.1016/j.blre.2021.100834.
    [29] VandendriesscheS,CambierS,ProostP,et al.Complement receptors and their role in leukocyte recruitment and phagocytosis[J].Front Cell Dev Biol,2021,9:624025.DOI: 10.3389/fcell.2021.624025.
    [30] SilkE,ZhaoH,WengH,et al.The role of extracellular histone in organ injury[J].Cell Death Dis,2017,8(5):e2812.DOI: 10.1038/cddis.2017.52.
    [31] KeragalaCB,DraxlerDF,McQuiltenZK,et al.Haemostasis and innate immunity - a complementary relationship: a review of the intricate relationship between coagulation and complement pathways[J].Br J Haematol,2018,180(6):782-798.DOI: 10.1111/bjh.15062.
    [32] GhateA,SharmaS,AgrawalP,et al.Differential expression of complement receptors CR1/2 and CR4 by murine M1 and M2 macrophages[J].Mol Immunol,2021,137:75-83.DOI: 10.1016/j.molimm.2021.06.003.
    [33] RodriguesM,KosaricN,BonhamCA,et al.Wound healing: a cellular perspective[J].Physiol Rev,2019,99(1):665-706.DOI: 10.1152/physrev.00067.2017.
    [34] LeeWY,HuYM,KoTL,et al.Glutamine modulates sepsis-induced changes to intestinal intraepithelial γδT lymphocyte expression in mice[J].Shock,2012,38(3):288-293.DOI: 10.1097/SHK.0b013e3182655932.
    [35] NguyenAV,SoulikaAM.The dynamics of the skin's immune system[J].Int J Mol Sci,2019,20(8):1811.DOI: 10.3390/ijms20081811.
    [36] CheskoDM,WilgusTA.Immune cells in cutaneous wound healing: a review of functional data from animal models[J].Int J Mol Sci,2022,23(5):2444.DOI: 10.3390/ijms23052444.
    [37] HanG,GengS,LiY,et al.γδT-cell function in sepsis is modulated by C5a receptor signalling[J].Immunology,2011,133(3):340-349.DOI: 10.1111/j.1365-2567.2011.03445.x.
    [38] SîrbulescuRF,ChungJY,EdmistonWJ,III,et al.Intraparenchymal application of mature B lymphocytes improves structural and functional outcome after contusion traumatic brain injury[J].J Neurotrauma,2019,36(17):2579-2589.DOI: 10.1089/neu.2018.6368.
    [39] MathernDR,HeegerPS.Molecules great and small: the complement system[J].Clin J Am Soc Nephrol,2015,10(9):1636-1650.DOI: 10.2215/CJN.06230614.
    [40] IwataY,YoshizakiA,KomuraK,et al.CD19, a response regulator of B lymphocytes, regulates wound healing through hyaluronan-induced TLR4 signaling[J].Am J Pathol,2009,175(2):649-660.DOI: 10.2353/ajpath.2009.080355.
    [41] SîrbulescuRF,BoehmCK,SoonE,et al.Mature B cells accelerate wound healing after acute and chronic diabetic skin lesions[J].Wound Repair Regen,2017,25(5):774-791.DOI: 10.1111/wrr.12584.
    [42] KiangJG,LedneyGD.Skin injuries reduce survival and modulate corticosterone, C-reactive protein, complement component 3, IgM, and prostaglandin E 2 after whole-body reactor-produced mixed field (n + γ-photons) irradiation[J].Oxid Med Cell Longev,2013,2013:821541.DOI: 10.1155/2013/821541.
    [43] BallRL,KeylounJW,Brummel-ZiedinsK,et al.Burn-induced coagulopathies: a comprehensive review[J].Shock,2020,54(2):154-167.DOI: 10.1097/SHK.0000000000001484.
    [44] AmaraU,FlierlMA,RittirschD,et al.Molecular intercommunication between the complement and coagulation systems[J].J Immunol,2010,185(9):5628-5636.DOI: 10.4049/jimmunol.0903678.
    [45] GikakisN,KhanMM,HiramatsuY,et al.Effect of factor Xa inhibitors on thrombin formation and complement and neutrophil activation during in vitro extracorporeal circulation[J].Circulation,1996,94(9 Suppl):SⅡ341-346.
    [46] van ErpIAM,van EssenTA,FluiterK,et al.Safety and efficacy of C1-inhibitor in traumatic brain injury (CIAO@TBI): study protocol for a randomized, placebo-controlled, multi-center trial[J].Trials,2021,22(1):874.DOI: 10.1186/s13063-021-05833-1.
  • 加载中
计量
  • 文章访问数:  273
  • HTML全文浏览量:  124
  • PDF下载量:  26
  • 被引次数: 0
出版历程
  • 收稿日期:  2022-07-26

目录

    /

    返回文章
    返回