HSP-Target of Therapeutic Agents in Sepsis Treatment

被引:20
作者
Vulczak, Anderson [1 ]
Rocha Catalao, Carlos Henrique [2 ]
Pedro de Freitas, Luiz Alexandre [3 ]
Alves Rocha, Maria Jose [1 ]
机构
[1] Univ Sao Paulo, Dept Basic & Oral Biol, Sch Dent Ribeirao Preto, BR-14040904 Ribeirao Preto, SP, Brazil
[2] Univ Sao Paulo, Dept Neurosci & Behav Sci, Ribeirao Preto Med Sch, BR-14040900 Ribeirao Preto, SP, Brazil
[3] Univ Sao Paulo, Dept Pharmaceut Sci, Sch Pharmaceut Sci Ribeirao Preto, BR-14040903 Ribeirao Preto, SP, Brazil
基金
巴西圣保罗研究基金会;
关键词
chaperone; systemic inflammation; immune response; organ dysfunction; heat shock protein; HEAT-SHOCK PROTEINS; INTERNATIONAL CONSENSUS DEFINITIONS; REGULATORY T-CELLS; SEPTIC SHOCK; CECAL LIGATION; ANIMAL-MODELS; POLYMICROBIAL SEPSIS; INFLAMMATORY CYTOKINES; LABORATORY MODELS; ENDOTOXEMIC MICE;
D O I
10.3390/ijms20174255
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
Sepsis is a syndrome characterized by a dysregulated inflammatory response, cellular stress, and organ injury. Sepsis is the main cause of death in intensive care units worldwide, creating need for research and new therapeutic strategies. Heat shock protein (HSP) analyses have recently been developed in the context of sepsis. HSPs have a cytoprotection role in stress conditions, signal to immune cells, and activate the inflammatory response. Hence, HSP analyses have become an important focus in sepsis research, including the investigation of HSPs targeted by therapeutic agents used in sepsis treatment. Many therapeutic agents have been tested, and their HSP modulation showed promising results. Nonetheless, the heterogeneity in experimental designs and the diversity in therapeutic agents used make it difficult to understand their efficacy in sepsis treatment. Therefore, future investigations should include the analysis of parameters related to the early and late immune response in sepsis, HSP localization (intra or extracellular), and time to the onset of treatment after sepsis. They also should consider the differences in experimental sepsis models. In this review, we present the main results of studies on therapeutic agents in targeting HSPs in sepsis treatment. We also discuss limitations and possibilities for future investigations regarding HSP modulators.
引用
收藏
页数:16
相关论文
共 141 条
[21]   Heat Shock Protein 72 Expressing Stress in Sepsis: Unbridgeable Gap between Animal and Human Studies-A Hypothetical "Comparative" Study [J].
Briassoulis, George ;
Briassouli, Efrossini ;
Fitrolaki, Diana-Michaela ;
Plati, Ioanna ;
Apostolou, Kleovoulos ;
Tavladaki, Theonymfi ;
Spanaki, Anna-Maria .
BIOMED RESEARCH INTERNATIONAL, 2014, 2014
[22]   Protective functions of intracellular heat-shock protein (HSP) 70-expression in patients with severe sepsis [J].
Bruemmer-Smith, S ;
Stüber, F ;
Schroeder, S .
INTENSIVE CARE MEDICINE, 2001, 27 (12) :1835-1841
[23]   Animal models of sepsis: Setting the stage [J].
Buras, JA ;
Holzmann, B ;
Sitkovsky, M .
NATURE REVIEWS DRUG DISCOVERY, 2005, 4 (10) :854-865
[24]   Pathway information for systems biology [J].
Cary, MP ;
Bader, GD ;
Sander, C .
FEBS LETTERS, 2005, 579 (08) :1815-1820
[25]   Celastrol: A Spectrum of Treatment Opportunities in Chronic Diseases [J].
Cascao, Rita ;
Fonseca, Joao E. ;
Moita, Luis F. .
FRONTIERS IN MEDICINE, 2017, 4
[26]   Severe sepsis and septic shock: Improving outcomes in the emergency department [J].
Catenacci, Michael H. ;
King, Kaira .
EMERGENCY MEDICINE CLINICS OF NORTH AMERICA, 2008, 26 (03) :603-+
[27]   Heat shock protein 70 confers cardiovascular protection during endotoxemia via inhibition of nuclear Factor-κB activation and inducible nitric oxide synthase expression in the rostral ventrolateral medulla [J].
Chan, JYH ;
Ou, CC ;
Wang, LL ;
Chan, SHH .
CIRCULATION, 2004, 110 (23) :3560-3566
[28]   Targeting Heat Shock Proteins in Cancer: A Promising Therapeutic Approach [J].
Chatterjee, Suman ;
Burns, Timothy F. .
INTERNATIONAL JOURNAL OF MOLECULAR SCIENCES, 2017, 18 (09)
[29]  
Chen Yu, 2007, Inflammation & Allergy Drug Targets, V6, P91
[30]   Heat shock factor 1 and heat shock proteins: Critical partners in protection against acute cell injury [J].
Christians, ES ;
Yan, LJ ;
Benjamin, IJ .
CRITICAL CARE MEDICINE, 2002, 30 (01) :S43-S50