Targeting neutrophils in sepsis

被引:44
作者
Sonego, Fabiane [1 ,2 ]
Alves-Filho, Jose Carlos [1 ]
Cunha, Fernando Queiroz [1 ]
机构
[1] Univ Sao Paulo, Dept Pharmacol, Ribeirao Preto Med Sch, Sao Paulo, Brazil
[2] Sanofi, Therapeut Strateg Unit Infect Dis, Toulouse, France
基金
巴西圣保罗研究基金会;
关键词
chemotaxis; innate immunity; neutrophil; organ damage; sepsis; CHEMOKINE RECEPTORS CXCR1; HEME OXYGENASE INHIBITION; INDUCIBLE NITRIC-OXIDE; EXTRACELLULAR TRAPS; IN-VIVO; POLYMICROBIAL SEPSIS; MIGRATION; FAILURE; EXPRESSION; CHEMOTAXIS;
D O I
10.1586/1744666X.2014.922876
中图分类号
R392 [医学免疫学]; Q939.91 [免疫学];
学科分类号
071005 [微生物学]; 100108 [医学免疫学];
摘要
Sepsis continues to have a high mortality rate worldwide. The multi-step effects of this syndrome make it difficult to develop a comprehensive understanding of its pathophysiology and to identify a direct treatment. Neutrophils play a major role in controlling infection. Interestingly, the recruitment of these cells to an infection site is markedly reduced in severe sepsis. The systemic activation of Toll-like receptors and high levels of TNF-alpha and nitric oxide are involved in the reduction of neutrophil recruitment due to down-regulation of CXCR2 in neutrophils. By contrast, CCR2 is expressed in neutrophils after sepsis induction and contributes to their recruitment to organs far from the infection site, which contributes to organ damage. This review provides an overview of the recent advances in the understanding of the role of neutrophils in sepsis, highlighting their potential as a therapeutic target.
引用
收藏
页码:1019 / 1028
页数:10
相关论文
共 90 条
[1]
Critical role for CCR2 and HMGB1 in induction of experimental endotoxic shock [J].
Alves, Jackson Nogueira ;
Pereira Pires, Karla Maria ;
Lanzetti, Manuella ;
Barroso, Marina Valente ;
Benjamim, Claudia Farias ;
Costa, Cristiane Aguiar ;
Resende, Angela Castro ;
Santos, Juliana Carvalho ;
Ribeiro, Marcelo Lima ;
Porto, Luis Cristovao ;
Valenca, Samuel Santos .
ARCHIVES OF BIOCHEMISTRY AND BIOPHYSICS, 2013, 537 (01) :72-81
[2]
Toll-like receptor 4 signaling leads to neutrophil migration impairment in polymicrobial sepsis [J].
Alves, JC ;
de Freitas, A ;
Russo, M ;
Cunha, FQ .
CRITICAL CARE MEDICINE, 2006, 34 (02) :461-470
[3]
NEUTROPHIL PARALYSIS IN SEPSIS [J].
Alves-Filho, Jose C. ;
Spiller, Fernando ;
Cunha, Fernando Q. .
SHOCK, 2010, 34 :15-21
[4]
Interleukin-33 attenuates sepsis by enhancing neutrophil influx to the site of infection [J].
Alves-Filho, Jose C. ;
Sonego, Fabiane ;
Souto, Fabricio O. ;
Freitas, Andressa ;
Verri, Waldiceu A., Jr. ;
Auxiliadora-Martins, Maria ;
Basile-Filho, Anibal ;
McKenzie, Andrew N. ;
Xu, Damo ;
Cunha, Fernando Q. ;
Liew, Foo Y. .
NATURE MEDICINE, 2010, 16 (06) :708-U113
[5]
Regulation of chemokine receptor by Toll-like receptor 2 is critical to neutrophil migration and resistance to polymicrobial sepsis [J].
Alves-Filho, Jose C. ;
Freitas, Andressa ;
Souto, Fabricio O. ;
Spiller, Fernando ;
Paula-Neto, Heitor ;
Silva, Joao S. ;
Gazzinelli, Ricardo T. ;
Teixeira, Mauro M. ;
Ferreira, Sergio H. ;
Cunha, Fernando Q. .
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 2009, 106 (10) :4018-4023
[6]
HMGB1 Is a Therapeutic Target for Sterile Inflammation and Infection [J].
Andersson, Ulf ;
Tracey, Kevin J. .
ANNUAL REVIEW OF IMMUNOLOGY, VOL 29, 2011, 29 :139-162
[7]
Impaired neutrophil chemotaxis in sepsis associates with GRK expression and inhibition of actin assembly and tyrosine phosphorylation [J].
Arraes, Sandra Mara A. ;
Freitas, Marta S. ;
da Silva, Simone V. ;
Neto, Heitor A. de Paula ;
Alves-Filho, Jose Carlos ;
Martins, Maria Auxiliadora ;
Basile-Filho, Anibal ;
Tavares-Murta, Beatriz M. ;
Barja-Fidalgo, Christina ;
Cunha, Fernando Q. .
BLOOD, 2006, 108 (09) :2906-2913
[8]
Inhibition of leukocyte rolling by nitric oxide during sepsis leads to reduced migration of active microbicidal neutrophils [J].
Benjamim, CF ;
Silva, JS ;
Fortes, ZB ;
Oliveira, MA ;
Ferreira, SH ;
Cunha, FQ .
INFECTION AND IMMUNITY, 2002, 70 (07) :3602-3610
[9]
Role of nitric oxide in the failure of neutrophil migration in sepsis [J].
Benjamim, CF ;
Ferreira, SH ;
Cunha, FD .
JOURNAL OF INFECTIOUS DISEASES, 2000, 182 (01) :214-223
[10]
THE ACCP-SCCM CONSENSUS CONFERENCE ON SEPSIS AND ORGAN FAILURE [J].
BONE, RC ;
SIBBALD, WJ ;
SPRUNG, CL .
CHEST, 1992, 101 (06) :1481-1482