Rational development of an mRNA antibody cocktail with extended therapeutic window against ricin intoxication

IF 4.7 3区 生物学 Q2 BIOTECHNOLOGY & APPLIED MICROBIOLOGY
Applied Microbiology and Biotechnology Pub Date : 2026-06-04 Epub Date: 2026-08-10 DOI:10.1007/s00253-026-13893-z
Mei Wu, Xi Luo, Pei-Yu Jiang, Qian Xu, Fei-Xue Du, Xiang Chen, Feng-Qin Yang, Zi-Jin Cui, Yu-Yan Li, Jie-Yu Chen, Tian-Shu Cao, Jing-Lin Wang, Wen-Wen Xin, Qing Ye, Cheng-Feng Qin
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引用次数: 0

Abstract

Ricin, a highly toxic protein derived from Ricinus communis, is recognized as a biological threat due to its high toxicity and the absence of approved specific antidotes. Monoclonal antibodies (mAbs) represent an emergency therapeutic for ricin intoxication. However, the short therapeutic window of existing antibody administration significantly limits their effectiveness in post-exposure treatment. To address these limitations, we developed a novel strategy leveraging lipid nanoparticle (LNP) encapsulated-mRNA platform for toxin antibodies delivery in vivo, enabling a time-saving, cost-effective approach that extends the therapeutic window. We designed and characterized two mRNA-encoded antibodies targeting the A chain (RTA) and B chain (RTB) of ricin, termed mRNA-43RCA and mRNA-Sy1H3, respectively. Then, each LNP-encapsulated mRNA antibody was combined to formulate the final mRNA antibody cocktail, termed mRNA-cocktail-LNP. In vivo studies demonstrated that a single administration of mRNA-cocktail-LNP enabled the rapid production of neutralizing antibodies, which conferred protection in mice against a subsequent lethal-dose ricin challenge. Additionally, mRNA-cocktail-LNP exhibited a significantly extended circulating half-life compared to its protein-format antibody in mice, and a single prophylactic dose provided complete protection against lethal ricin challenge for at least 14 days post administration. More importantly, mRNA-cocktail-LNP conferred protection even when administered 10 h after lethal-dose ricin exposure, demonstrating an extended therapeutic window. Taken together, our results indicate that mRNA-cocktail-LNP represents a promising therapeutic candidate against ricin intoxication, highlighting the potential of mRNA-LNP platform as a universal strategy for developing antibody-based countermeasures against ricin and a broad spectrum of other biological threats.

• An mRNA antibody cocktail (mRNA-cocktail-LNP) was designed to against RT and protect the mice from challenge with ricin both prophylactic and post-exposure treatments

• mRNA-cocktail-LNP with a prolonged half-life compared to its protein format.

• mRNA-cocktail-LNP significantly extended the limited therapeutic window to 10 h for ricin intoxication treatment.

合理研制具有延长治疗窗口期的蓖麻毒素中毒mRNA抗体鸡尾酒。
蓖麻毒素是一种从蓖麻中提取的高毒性蛋白质,由于其高毒性和缺乏经批准的特异性解毒剂而被认为是一种生物威胁。单克隆抗体(mab)是蓖麻毒素中毒的一种紧急治疗方法。然而,现有抗体给药的短治疗窗口极大地限制了它们在暴露后治疗中的有效性。为了解决这些限制,我们开发了一种利用脂质纳米颗粒(LNP)封装mrna平台的新策略,用于毒素抗体的体内递送,从而节省时间,降低成本,延长治疗窗口期。我们设计并鉴定了两种针对蓖麻毒素A链(RTA)和B链(RTB)的mrna编码抗体,分别命名为mRNA-43RCA和mRNA-Sy1H3。然后,将每个lnp封装的mRNA抗体组合成最终的mRNA抗体鸡尾酒,称为mRNA-cocktail- lnp。体内研究表明,单次给药mrna -鸡尾酒- lnp能够快速产生中和抗体,从而保护小鼠免受随后致命剂量的蓖麻毒素攻击。此外,mRNA-cocktail-LNP在小鼠体内的循环半衰期比其蛋白形式抗体明显延长,并且单次预防性剂量至少在给药后14天内对致命蓖麻毒素攻击提供完全保护。更重要的是,mrna -鸡尾酒- lnp即使在致命剂量蓖麻毒素暴露10小时后也具有保护作用,这表明治疗窗口期延长。综上所示,我们的研究结果表明,mRNA-cocktail-LNP是一种很有前途的治疗蓖麻毒素中毒的候选药物,突出了mRNA-LNP平台作为开发针对蓖麻毒素和其他广泛生物威胁的基于抗体的对策的通用策略的潜力。•设计了一种mRNA抗体鸡尾酒(mRNA-cocktail- lnp)来对抗RT,并保护小鼠免受蓖麻毒素预防和暴露后处理的攻击•mRNA-cocktail- lnp与其蛋白质格式相比具有较长的半衰期。•mRNA-cocktail-LNP显著延长了蓖麻毒素中毒治疗的有限治疗窗口至10小时。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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来源期刊
Applied Microbiology and Biotechnology
Applied Microbiology and Biotechnology 工程技术-生物工程与应用微生物
CiteScore
10.00
自引率
4.00%
发文量
535
审稿时长
2 months
期刊介绍: Applied Microbiology and Biotechnology focusses on prokaryotic or eukaryotic cells, relevant enzymes and proteins; applied genetics and molecular biotechnology; genomics and proteomics; applied microbial and cell physiology; environmental biotechnology; process and products and more. The journal welcomes full-length papers and mini-reviews of new and emerging products, processes and technologies.
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