INSERM LNC, UMR1231, Dijon, France.
University Bourgogne Franche-Comté, LNC UMR1231, Dijon, France.
Sci Rep. 2017 Jun 8;7(1):3053. doi: 10.1038/s41598-017-03285-9.
Although plasma phospholipid transfer protein (PLTP) has been mainly studied in the context of atherosclerosis, it shares homology with proteins involved in innate immunity. Here, we produced active recombinant human PLTP (rhPLTP) in the milk of new lines of transgenic rabbits. We successfully used rhPLTP as an exogenous therapeutic protein to treat endotoxemia and sepsis. In mouse models with injections of purified lipopolysaccharides or with polymicrobial infection, we demonstrated that rhPLTP prevented bacterial growth and detoxified LPS. In further support of the antimicrobial effect of PLTP, PLTP-knocked out mice were found to be less able than wild-type mice to fight against sepsis. To our knowledge, the production of rhPLTP to counter infection and to reduce endotoxemia and its harmful consequences is reported here for the first time. This paves the way for a novel strategy to satisfy long-felt, but unmet needs to prevent and treat sepsis.
尽管血浆磷脂转移蛋白 (PLTP) 主要在动脉粥样硬化的背景下进行研究,但它与参与先天免疫的蛋白质具有同源性。在这里,我们在新的转基因兔系的乳汁中产生了活性的重组人 PLTP (rhPLTP)。我们成功地将 rhPLTP 用作治疗内毒素血症和败血症的外源性治疗蛋白。在接受纯化脂多糖注射或多微生物感染的小鼠模型中,我们证明 rhPLTP 可防止细菌生长并使 LPS 解毒。进一步支持 PLTP 的抗菌作用,与野生型小鼠相比,PLTP 敲除小鼠对抗败血症的能力降低。据我们所知,本研究首次报道了 rhPLTP 的产生可用于对抗感染、减少内毒素血症及其有害后果。这为满足长期存在但未得到满足的预防和治疗败血症的需求开辟了一条新途径。