Gaitonde Puneet, Purohit Vivek S, Balu-Iyer Sathy V
Department of Pharmaceutical Sciences, University at Buffalo, The State University of New York, Buffalo, NY 14214, United States.
Eur J Pharm Sci. 2015 Jan 23;66:157-62. doi: 10.1016/j.ejps.2014.10.010. Epub 2014 Oct 20.
Hemophilia A is a bleeding disorder caused by the deficiency of an important coagulation factor; Factor VIII (FVIII). Replacement therapy using exogenously administered recombinant FVIII is the most commonly used method of treatment. However, approximately 30% of Hemophilia A patients develop neutralizing antibodies (Nabs) against the recombinant protein. Nabs abolish FVIII activity and drastically influence efficacy of the protein. The immunogenic epitopes of FVIII reside predominantly in the C2 domain of FVIII. However, the C2 domain also contains a lipid binding region. O-Phospho-L-Serine (OPLS) which is the head-group moiety of phosphatidylserine, interacts with the lipid binding region of FVIII. Previous studies have shown that FVIII complexed with OPLS lowered Nab development against FVIII following subcutaneous administration. In dendritic cell-T-cell co-culture studies, OPLS treatment increased the secretion of immunosuppressive cytokines (Transforming Growth Factor-β and Interleukin-10), and simultaneously decreased pro-inflammatory IL-17 cytokine. Here, we investigated FVIII immune response and pharmacokinetics upon intravenous administration of FVIII-OPLS complex. We studied the effect of FVIII-OPLS complex on the interaction between a professional antigen presenting cell; dendritic cell and T-cell, and T-cell clonal expansion. Pharmacokinetics parameters were estimated following intravenous administration of FVIII and FVIII-OPLS. The results suggest that OPLS lowers FVIII immune response following intravenous administration. OPLS also hinders FVIII-specific T-cell clonal proliferation and preserves FVIII PK profile. Thus, the ease of protein-lipid complexation, preservation of FVIII activity and in vivo behavior, and improved in vitro FVIII stability, makes OPLS an attractive excipient in the preparation of next generation or biosimilar FVIII products with improved safety profile.
甲型血友病是一种由重要凝血因子——凝血因子VIII(FVIII)缺乏引起的出血性疾病。使用外源性给予的重组FVIII进行替代疗法是最常用的治疗方法。然而,约30%的甲型血友病患者会产生针对重组蛋白的中和抗体(Nabs)。Nabs会消除FVIII活性,并严重影响该蛋白的疗效。FVIII的免疫原性表位主要位于FVIII的C2结构域。然而,C2结构域也包含一个脂质结合区域。O-磷酸-L-丝氨酸(OPLS)是磷脂酰丝氨酸的头部基团部分,与FVIII的脂质结合区域相互作用。先前的研究表明,与OPLS复合的FVIII皮下给药后可降低针对FVIII的Nab产生。在树突状细胞-T细胞共培养研究中,OPLS处理增加了免疫抑制细胞因子(转化生长因子-β和白细胞介素-10)的分泌,同时减少了促炎IL-17细胞因子。在此,我们研究了静脉注射FVIII-OPLS复合物后FVIII的免疫反应和药代动力学。我们研究了FVIII-OPLS复合物对专业抗原呈递细胞(树突状细胞)与T细胞之间相互作用以及T细胞克隆扩增的影响。静脉注射FVIII和FVIII-OPLS后估计药代动力学参数。结果表明,OPLS可降低静脉给药后FVIII的免疫反应。OPLS还阻碍FVIII特异性T细胞克隆增殖,并保留FVIII的药代动力学特征。因此,蛋白-脂质复合的简便性、FVIII活性和体内行为的保留以及体外FVIII稳定性的提高,使OPLS成为制备具有改善安全性的下一代或生物类似FVIII产品的有吸引力的辅料。