Department of Anesthesiology, Washington University School of Medicine, 660 S. Euclid Ave., St. Louis, MO 63110, USA.
Biochem Biophys Res Commun. 2011 Oct 14;414(1):37-43. doi: 10.1016/j.bbrc.2011.09.017. Epub 2011 Sep 12.
Secondary infection following septic insult represents a significant cause of morbidity and mortality in hospitalized patients. Sepsis induced immunosuppression is a major factor in the host's susceptibility to nosocomial infections and Candida albicans accounts for a growing number of these. Given the importance of improving our understanding of the immune response to sepsis and the increasing rates of C. albicans infections, we sought to develop a murine model of double injury consisting of primary peritonitis, i.e., cecal ligation and puncture (CLP), followed by a secondary challenge of C. albicans. As observed in previous work, after primary injury the immune profile of the host changes over time. Therefore, while keeping the mortality rates from the respective individual injuries low, we altered the timing of the secondary injury between two post-CLP time points, day two and day four. Mice subjected to C. albicans infection following CLP have significantly different survival rates dependent upon timing of secondary injury. Animals challenged with C. albicans at two days post CLP had 91% mortality whereas animals challenged at four days had 47% mortality. This improvement in survival at four days was associated with restoration of innate cell populations and as evidenced by stimulated splenocytes, increases in certain inflammatory cytokines. In addition, we show that susceptibility to C. albicans infection following CLP is dependent upon the depth of immunosuppression. Although at four days post-CLP there is a partial reconstitution of the immune system, these animals remain more susceptible to infection compared to their single injury (C. albicans alone) counterparts. Collectively, these studies demonstrate that immunosuppression following initial septic insult changes over time. This novel, two hit model of CLP followed by Candida provides additional insight into the immune compromised state created by primary peritonitis, and thereby opens up another avenue of investigation into the causes and possible cures of an emerging clinical problem.
二次感染继发于感染性休克,是导致住院患者发病率和死亡率升高的重要原因。感染性休克导致的免疫抑制是宿主易发生医院获得性感染和白色念珠菌感染的主要因素,且后者的比例正在不断增加。鉴于深入了解宿主对感染性休克的免疫反应以及白色念珠菌感染率不断上升的重要性,我们试图建立一种由原发腹膜炎(即盲肠结扎穿孔术,CLP)后继发白色念珠菌感染的双重损伤的小鼠模型。正如之前的研究观察到的,在原发损伤后,宿主的免疫特征会随时间发生变化。因此,在保持各自单一损伤的死亡率较低的情况下,我们改变了继发损伤的时机,分别在 CLP 后两天和四天进行。CLP 后继发白色念珠菌感染的小鼠的存活率因继发损伤的时机不同而有显著差异。在 CLP 后两天接受白色念珠菌感染的动物的死亡率为 91%,而在四天接受感染的动物的死亡率为 47%。四天时存活率的提高与固有细胞群体的恢复有关,这一点从刺激后的脾细胞和某些炎症细胞因子的增加可以得到证明。此外,我们还表明,CLP 后继发白色念珠菌感染的易感性取决于免疫抑制的程度。尽管在 CLP 后四天,免疫系统有部分重建,但与单一损伤(仅白色念珠菌感染)的对照动物相比,这些动物仍然更容易感染。总之,这些研究表明,初始感染性休克后的免疫抑制会随时间而变化。这种新的、两次打击的 CLP 继发白念珠菌感染模型提供了对原发腹膜炎引起的免疫抑制状态的更深入了解,从而为研究这一新兴临床问题的病因和可能的治疗方法开辟了另一条途径。