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Proteolytic cleavage of antigen extends the durability of an anti-PCSK9 monoclonal antibody

机译:抗原的蛋白水解切割可延长抗PCSK9单克隆抗体的寿命

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摘要

Lilly PCSK9 antibody LY3015014 (LY) is a monoclonal antibody (mAb) that neutralizes proprotein convertase subtilisin-kexin type 9 (PCSK9). LY decreases LDL cholesterol in monkeys and, unlike other PCSK9 mAbs, does not cause an accumulation of intact PCSK9 in serum. Comparing the epitope of LY with other clinically tested PCSK9 mAbs, it was noted that the LY epitope excludes the furin cleavage site in PCSK9, whereas other mAbs span this site. In vitro exposure of PCSK9 to furin resulted in degradation of PCSK9 bound to LY, whereas cleavage was blocked by other mAbs. These other mAbs caused a significant accumulation of serum PCSK9 and displayed a shorter duration of LDL-cholesterol lowering than LY when administered to mice expressing the WT human PCSK9. In mice expressing a noncleavable variant of human PCSK9, LY behaved like a cleavage-blocking mAb, in that it caused significant PCSK9 accumulation, its duration of LDL lowering was reduced, and its clearance (CL) from serum was accelerated. Thus, LY neutralizes PCSK9 and allows its proteolytic degradation to proceed, which limits PCSK9 accumulation, reduces the CL rate of LY, and extends its duration of action. PCSK9 mAbs with this property are likely to achieve longer durability and require lower doses than mAbs that cause antigen to accumulate.
机译:礼来PCSK9抗体LY3015014(LY)是一种单克隆抗体(mAb),可中和9型前蛋白转化酶枯草杆菌蛋白酶-kexin(PCSK9)。 LY可降低猴子中的LDL胆固醇,与其他PCSK9 mAb不同,LY不会引起完整PCSK9在血清中的积累。将LY的表位与其他经过临床测试的PCSK9 mAb进行比较,注意到LY的表位不包括PCSK9中的弗林蛋白酶切割位点,而其他mAb跨越该位点。 PCSK9在弗林蛋白酶的体外暴露导致与LY结合的PCSK9降解,而裂解被其他mAb阻断。当对表达WT人PCSK9的小鼠给药时,这些其他mAb导致血清PCSK9大量积聚,并且LLY降低的持续时间比LY短。在表达人PCSK9不可裂解变异体的小鼠中,LY的行为类似于裂解阻断mAb,因为它引起PCSK9大量积聚,LDL降低的持续时间减少,并加速了其从血清中的清除(CL)。因此,LY可以中和PCSK9,并使其蛋白降解继续进行,从而限制PCSK9的积累,降低LY的CL率,并延长其作用时间。具有这种特性的PCSK9 mAb可能比导致抗原积聚的mAb具有更长的耐久性,并且需要的剂量更低。

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