ACS Chem Neurosci. 2023 Aug 16;14(16):2849-2856. doi: 10.1021/acschemneuro.3c00455. Epub 2023 Aug 3.
The opioid overdose crisis primarily driven by potent synthetic opioids resulted in more than 500,000 deaths in the US over the last 20 years. Though naloxone, a short-acting medication, remains the primary treatment option for temporarily reversing opioid overdose effects, alternative countermeasures are needed. Monoclonal antibodies present a versatile therapeutic opportunity that can be tailored to synthetic opioids and help prevent post-treatment renarcotization. The ultrapotent analog carfentanil is especially concerning due to its unique pharmacological properties. With this in mind, we generated a fully human antibody through a drug-specific B cell sorting strategy with a combination of carfentanil and fentanyl probes. The resulting pan-specific antibody was further optimized through scFv phage display, producing C10-S66K. This monoclonal antibody displays high affinity to carfentanil, fentanyl, and other analogs and reversed carfentanil-induced respiratory depression. Additionally, X-ray crystal structures with carfentanil and fentanyl bound provided structural insight into key drug:antibody interactions.
阿片类药物过量危机主要由强效合成阿片类药物驱动,在过去 20 年中导致美国超过 50 万人死亡。尽管纳洛酮是一种短效药物,仍然是暂时逆转阿片类药物过量作用的主要治疗选择,但仍需要替代对策。单克隆抗体提供了一种多功能的治疗机会,可以针对合成阿片类药物进行定制,并有助于防止治疗后再成瘾。超强效类似物卡芬太尼因其独特的药理学特性而特别令人担忧。考虑到这一点,我们通过使用卡芬太尼和芬太尼探针的药物特异性 B 细胞分选策略生成了一种全人源抗体。所得的 pan 特异性抗体通过 scFv 噬菌体展示进一步优化,产生 C10-S66K。这种单克隆抗体对卡芬太尼、芬太尼和其他类似物具有高亲和力,并逆转了卡芬太尼引起的呼吸抑制。此外,与卡芬太尼和芬太尼结合的 X 射线晶体结构提供了对关键药物-抗体相互作用的结构见解。