Guo Zhongyuan, Zhu Audrey T, Wei Xiaoli, Jiang Yao, Yu Yiyan, Noh Ilkoo, Gao Weiwei, Fang Ronnie H, Zhang Liangfang
Department of NanoEngineering, Chemical Engineering Program, Shu and K.C. Chien and Peter Farrell Collaboratory, University of California San Diego, La Jolla, CA, 92093, USA.
Division of Host-Microbe Systems and Therapeutics, Department of Pediatrics, University of California San Diego, La Jolla, CA, 92093, USA.
Bioact Mater. 2024 May 9;38:321-330. doi: 10.1016/j.bioactmat.2024.05.006. eCollection 2024 Aug.
Given their dangerous effects on the nervous system, neurotoxins represent a significant threat to public health. Various therapeutic approaches, including chelating agents, receptor decoys, and toxin-neutralizing antibodies, have been explored. While prophylactic vaccines are desirable, it is oftentimes difficult to effectively balance their safety and efficacy given the highly dangerous nature of neurotoxins. To address this, we report here on a nanovaccine against neurotoxins that leverages the detoxifying properties of cell membrane-coated nanoparticles. A genetically modified cell line with constitutive overexpression of the α7 nicotinic acetylcholine receptor is developed as a membrane source to generate biomimetic nanoparticles that can effectively and irreversibly bind to α-bungarotoxin, a model neurotoxin. This abrogates the biological activity of the toxin, enabling the resulting nanotoxoid to be safely delivered into the body and processed by the immune system. When co-administered with an immunological adjuvant, a strong humoral response against α-bungarotoxin is generated that protects vaccinated mice against a lethal dose of the toxin. Overall, this work highlights the potential of using genetic modification strategies to develop nanotoxoid formulations against various biological threats.
鉴于神经毒素对神经系统具有危险影响,它们对公众健康构成重大威胁。人们已经探索了各种治疗方法,包括螯合剂、受体诱饵和毒素中和抗体。虽然预防性疫苗是理想的,但鉴于神经毒素的高度危险性,往往难以有效平衡其安全性和有效性。为了解决这一问题,我们在此报告一种针对神经毒素的纳米疫苗,它利用了细胞膜包被纳米颗粒的解毒特性。开发了一种组成型过表达α7烟碱型乙酰胆碱受体的基因改造细胞系作为膜源,以生成能够有效且不可逆地结合模型神经毒素α-银环蛇毒素的仿生纳米颗粒。这消除了毒素的生物活性,使生成的纳米类毒素能够安全地递送至体内并由免疫系统进行处理。当与免疫佐剂共同给药时,会产生针对α-银环蛇毒素的强烈体液反应,从而保护接种疫苗的小鼠免受致死剂量毒素的侵害。总体而言,这项工作突出了利用基因改造策略开发针对各种生物威胁的纳米类毒素制剂的潜力。