programmed death-1 levels correlate with increased mortality, nosocomial infection and immune dysfunctions in septic shock patients程序性死亡1水平与死亡率增加,脓毒性休克患者的院内感染和免疫功能紊乱.pdfVIP

programmed death-1 levels correlate with increased mortality, nosocomial infection and immune dysfunctions in septic shock patients程序性死亡1水平与死亡率增加,脓毒性休克患者的院内感染和免疫功能紊乱.pdf

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programmed death-1 levels correlate with increased mortality, nosocomial infection and immune dysfunctions in septic shock patients程序性死亡1水平与死亡率增加,脓毒性休克患者的院内感染和免疫功能紊乱

Guignant et al. Critical Care 2011, 15:R99 /content/15/2/R99 RESEARCH Open Access Programmed death-1 levels correlate with increased mortality, nosocomial infection and immune dysfunctions in septic shock patients 1 2 3 1 4 1 Caroline Guignant , Alain Lepape , Xin Huang , Hakim Kherouf , Laure Denis , Françoise Poitevin , 1 5 5 6 3 Christophe Malcus , Aurélie Chéron , Bernard Allaouchiche , François Gueyffier , Alfred Ayala , Guillaume Monneret1*† and Fabienne Venet1† Abstract Introduction: Septic shock remains a major health care problem worldwide. Sepsis-induced immune alterations are thought to play a major role in patients’ mortality and susceptibility to nosocomial infections. Programmed death-1 (PD-1) receptor system constitutes a newly described immunoregulatory pathway that negatively controls immune responses. It has recently been shown that PD-1 knock-out mice exhibited a lower mortality in response to experimental sepsis. The objective of the present study was to investigate PD-1-related molecule expressions in septic shock patients. Methods: This prospective and observational study included 64 septic shock patients, 13 trauma patients and 49 healthy individuals. PD-1-related-molecule expressions were measured by flow cytometry on circulating leukocytes. Plasmatic interleukin (IL)-10 concentration as well as ex vivo mitogen-induced lymphocyte proliferation were assessed. Results: We observed that septic shock patients displayed increased PD-1, PD-Ligand1 (PD-L1) and PD-L2 monocyte expressions and enhanced PD-1 and PD-L1 CD4+ T lymphocyte expressions at day 1-2 and 3-5 after the onse

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