Department of Microbiology and Immunology, Albert Einstein College of Medicine, Bronx, NY 10461, USA.
Mapp Biopharmaceutical, San Diego, CA 92121, USA.
Cell Host Microbe. 2019 Jan 9;25(1):39-48.e5. doi: 10.1016/j.chom.2018.12.004.
Passive administration of monoclonal antibodies (mAbs) is a promising therapeutic approach for Ebola virus disease (EVD). However, all mAbs and mAb cocktails that have entered clinical development are specific for a single member of the Ebolavirus genus, Ebola virus (EBOV), and ineffective against outbreak-causing Bundibugyo virus (BDBV) and Sudan virus (SUDV). Here, we advance MBP134, a cocktail of two broadly neutralizing human mAbs, ADI-15878 from an EVD survivor and ADI-23774 from the same survivor but specificity-matured for SUDV GP binding affinity, as a candidate pan-ebolavirus therapeutic. MBP134 potently neutralized all ebolaviruses and demonstrated greater protective efficacy than ADI-15878 alone in EBOV-challenged guinea pigs. A second-generation cocktail, MBP134, engineered to effectively harness natural killer (NK) cells afforded additional improvement relative to its precursor in protective efficacy against EBOV and SUDV in guinea pigs. MBP134 is an optimized mAb cocktail suitable for evaluation as a pan-ebolavirus therapeutic in nonhuman primates.
被动给予单克隆抗体(mAbs)是治疗埃博拉病毒病(EVD)的一种很有前景的治疗方法。然而,所有进入临床开发的 mAbs 和 mAb 鸡尾酒都针对埃博拉病毒属的单一成员埃博拉病毒(EBOV),对引起暴发的布迪Bugyo 病毒(BDBV)和苏丹病毒(SUDV)无效。在这里,我们提出了 MBP134,它是由一名 EVD 幸存者的 ADI-15878 和同一名幸存者但特异性成熟的 ADI-23774 两种广泛中和的人源 mAbs 组成的鸡尾酒,作为一种潜在的泛埃博拉病毒治疗候选药物。MBP134 可有效中和所有埃博拉病毒,并在 EBOV 挑战的豚鼠中显示出比 ADI-15878 单独使用更高的保护效力。第二代鸡尾酒 MBP134,经过工程设计可有效利用自然杀伤(NK)细胞,相对于其前体在保护效力方面对 EBOV 和 SUDV 的保护效力有了进一步的提高。MBP134 是一种经过优化的 mAb 鸡尾酒,适合在非人类灵长类动物中作为泛埃博拉病毒治疗药物进行评估。