Current views on the mechanisms of immune responses to trauma and infection

被引:82
作者
Binkowska, Aneta Malgorzata [1 ,2 ]
Michalak, Grzegorz [1 ]
Slotwinski, Robert [3 ,4 ]
机构
[1] Med Univ Warsaw, Dept Emergency Med, Warsaw, Poland
[2] Med Univ Warsaw, Dept Disaster Med, Warsaw, Poland
[3] Med Univ Warsaw, Dept Immunol Biochem & Nutr, Warsaw, Poland
[4] Polish Acad Sci, Med Res Ctr, Dept Surg Res & Transplantol, Warsaw, Poland
关键词
sepsis; SIRS; CARS; PICS; MODS; innate immune response; SYSTEMIC INFLAMMATORY RESPONSE; MULTIPLE ORGAN FAILURE; SEVERE SEPSIS; ANTIINFLAMMATORY RESPONSE; INTERLEUKIN-2; SYNTHESIS; BURN INJURY; EPIDEMIOLOGY; PATHOGENESIS; THYMOPENTIN; DYSFUNCTION;
D O I
10.5114/ceji.2015.52835
中图分类号
R392 [医学免疫学]; Q939.91 [免疫学];
学科分类号
100102 ;
摘要
According to the World Health Organization, post-traumatic mortality rates are still very high and show an increasing tendency. Disorders of innate immune response that may increase the risk of serious complications play a key role in the immunological system response to trauma and infection. The mechanism of these disorders is multifactorial and is still poorly understood. The changing concepts of systemic inflammatory response syndrome (SIRS) and compensatory anti-inflammatory response syndrome (CARS) early inflammatory response, presented in this work, have been extended to genetic studies. Overexpression of genes and increased production of immune response mediators are among the main causes of multiple organ dysfunction syndrome (MODS). Changes in gene expression detected early after injury precede the occurrence of subsequent complications with a typical clinical picture. Rapid depletion of energy resources leads to immunosuppression and persistent inflammation and immune suppression catabolism syndrome (PICS). Early diagnosis of immune disorders and appropriate nutritional therapy can significantly reduce the incidence of complications, length of hospital stay, and mortality. The study presents the development of knowledge and current views explaining the mechanisms of the immune response to trauma and infection.
引用
收藏
页码:206 / 216
页数:11
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