Mechanism of Activated Protein C Action in Sepsis Therapy

描述（由申请人提供）：脓毒症是一种对微生物感染的全身性炎症宿主反应，严重脓毒症和脓毒性休克患者的死亡率分别达到30%至70%。重组活化蛋白C（APC）是第一个，也是迄今为止唯一一个被证明可以降低严重脓毒症患者死亡率的药物，但可能导致严重出血，并且似乎在儿童和不太严重的脓毒症患者中缺乏疗效。介导APC在患者中的治疗效果的机制以及APC治疗的局限性的原因在很大程度上是未知的。目前的建议采用细菌性脓毒症的小鼠模型，重组APC的诱变，和转基因小鼠品系，以解决在脓毒症的治疗APC功能的关键方面。初步数据表明工作假设，APC的抗凝活性，目前的临床给药的基础上，可能不仅会增加严重出血的风险，而且会损害纤维蛋白依赖性清除细菌病原体，从而降低APC治疗的疗效。相反，APC通过受体EPCR和PAR 1的细胞信号传导活性似乎是APC治疗降低脓毒症死亡率的主要机制。因此，与正常APC相比，具有选择性降低的抗凝剂但正常信号传导活性的重组APC变体在败血症的鼠模型中表现出显著的功效增益。目的：1、阐明APC的抗凝活性对宿主抗菌防御的不利影响，并揭示其分子机制;和（AIM 2）精确定位APC信号活性靶向的关键受体和细胞组分以降低脓毒症死亡率，（AIM 3）提供了第一个证据，是否可以预期具有选择性降低的抗凝活性的重组APC变体的积极给药可以改善APC治疗的总体疗效和安全性。公共卫生相关性：仅在美国，微生物感染后的严重脓毒症每年影响超过700，000名患者，并且导致约9%的所有原因的死亡。重组活化蛋白C（APC）是迄今为止唯一可用的脓毒症药物，可降低（约6%）严重脓毒症患者的绝对死亡率，但可能导致严重出血，并且在儿童和不太严重的脓毒症患者中缺乏疗效。我们将研究选择性地参与关键分子和细胞靶点以促进生存，但缺乏正常APC的有害副作用的新型APC变体是否可以显着提高APC治疗的疗效。

DESCRIPTION (provided by applicant): Sepsis is a systemic inflammatory host response to microbial infection, with mortality of patients with severe sepsis and septic shock reaching 30% to 70%, respectively. Recombinant activated protein C (APC) is the first, and as yet only drug demonstrated to reduce mortality of patients with severe sepsis, but may cause severe bleeding, and appears to lack efficacy in children and in patients with less than severe sepsis. The mechanisms mediating the therapeutic efficacy of APC in patients, and the reasons for the limitations of APC therapy are largely unknown. The current proposal employs murine models of bacterial sepsis, mutagenesis of recombinant APC, and transgenic mouse strains to address critical aspects of APC function in the treatment of sepsis. Preliminary data suggest the working hypothesis that the anticoagulant activity of APC, on which current clinical dosing is based, may not only increase the risk of severe bleeding, but also impair the fibrin-dependent clearance of bacterial pathogens and thereby diminish the efficacy of APC therapy. In contrast, the cell signaling activity of APC via the receptors EPCR and PAR1 appears to be the predominant mechanism underlying sepsis mortality reduction by APC therapy. Accordingly, recombinant APC variants with selectively reduced anticoagulant, but normal signaling activity exhibit a striking gain of efficacy in murine models of sepsis, as compared to normal APC. Proposed experiments will (AIM 1) demonstrate the harmful effects of APC's anticoagulant activity on the antibacterial host defense and reveal the underlying molecular mechanism; and (AIM 2) pinpoint the critical receptors and cellular components targeted by APC's signaling activity to reduce sepsis mortality, and (AIM 3) provide first evidence whether aggressive dosing of recombinant APC variants with selectively reduced anticoagulant activity may be expected to improve the overall efficacy and safety of APC therapy. PUBLIC HEALTH RELEVANCE: Severe sepsis after microbial infection affects in excess of 700,000 patients annually in the US alone, and is responsible for ~9% of deaths from all causes. Recombinant activated protein C (APC) is the as yet only available sepsis drug shown to reduce (by ~6%) absolute mortality of patients with severe sepsis, but may cause severe bleeding, and lacks efficacy in children and in patients with less than severe sepsis. We will investigate whether novel APC variants that selectively engage the critical molecular and cellular targets to promote survival, but lack the harmful side effects of normal APC can significantly improve the efficacy of APC therapy.