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一种对蓖麻毒素同工型 D 和 E 具有高亲和力的单克隆抗体可提供针对蓖麻毒素中毒的强力保护。

A Monoclonal Antibody with a High Affinity for Ricin Isoforms D and E Provides Strong Protection against Ricin Poisoning.

机构信息

Département Médicaments et Technologies pour la Santé (DMTS), SPI, Université Paris Saclay, CEA, INRAE, 91191 Gif-sur-Yvette, France.

Microbiology and Infectious Diseases Department, French Armed Forces Biomedical Research Institute, 91220 Brétigny-sur-Orge, France.

出版信息

Toxins (Basel). 2024 Sep 24;16(10):412. doi: 10.3390/toxins16100412.

DOI:10.3390/toxins16100412
PMID:39453188
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC11510859/
Abstract

Ricin is a highly potent toxin that has been used in various attempts at bioterrorism worldwide. Although a vaccine for preventing ricin poisoning (RiVax™) is in clinical development, there are currently no commercially available prophylaxis or treatments for ricin intoxication. Numerous studies have highlighted the potential of passive immunotherapy using anti-ricin monoclonal antibodies (mAbs) and have shown promising results in preclinical models. In this article, we describe the neutralizing and protective efficacy of a new generation of high-affinity anti-ricin mAbs, which bind and neutralize very efficiently both ricin isoforms D and E in vitro through cytotoxicity cell assays. In vivo, protection assay revealed that one of these mAbs (RicE5) conferred over 90% survival in a murine model challenged intranasally with a 5 LD of ricin and treated by intravenous administration of the mAbs 6 h post-intoxication. Notably, a 35% survival rate was observed even when treatment was administered 24 h post-exposure. Moreover, all surviving mice exhibited long-term immunity to high ricin doses. These findings offer promising results for the clinical development of a therapeutic candidate against ricin intoxication and may also pave the way for novel vaccination strategies against ricin or other toxins.

摘要

蓖麻毒素是一种效力极强的毒素,已在全球范围内的各种生物恐怖袭击尝试中被使用。虽然预防蓖麻毒素中毒的疫苗(RiVax™)正在临床开发中,但目前尚无商业可用的预防或治疗蓖麻中毒的方法。许多研究强调了使用抗蓖麻毒素单克隆抗体(mAbs)进行被动免疫治疗的潜力,并在临床前模型中显示出了有希望的结果。在本文中,我们描述了新一代高亲和力抗蓖麻毒素 mAbs 的中和和保护效力,这些 mAbs 通过细胞毒性测定在体外非常有效地结合并中和两种蓖麻毒素同工型 D 和 E。在体内保护试验中,发现这些 mAbs 中的一种(RicE5)在经鼻内给予 5 LD 蓖麻毒素的小鼠模型中,通过静脉注射 mAbs 进行治疗,可使 90%以上的小鼠存活,并且在暴露后 24 小时给予治疗时,仍观察到 35%的存活率。此外,所有存活的小鼠都对高剂量的蓖麻毒素表现出长期免疫力。这些发现为开发针对蓖麻毒素中毒的治疗候选药物的临床开发提供了有希望的结果,并且也可能为针对蓖麻毒素或其他毒素的新型疫苗接种策略铺平道路。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/978d/11510859/70b9e685fbf8/toxins-16-00412-g010.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/978d/11510859/0d05f58e6d8f/toxins-16-00412-g001.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/978d/11510859/467b80d733ab/toxins-16-00412-g002.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/978d/11510859/6ea70da36d55/toxins-16-00412-g003.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/978d/11510859/3df96a19bdc4/toxins-16-00412-g004.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/978d/11510859/71f74c82b772/toxins-16-00412-g005.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/978d/11510859/06c07ad8c2f9/toxins-16-00412-g006.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/978d/11510859/357bd7f66084/toxins-16-00412-g007.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/978d/11510859/6a025b8c3672/toxins-16-00412-g008.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/978d/11510859/74c383447561/toxins-16-00412-g009.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/978d/11510859/70b9e685fbf8/toxins-16-00412-g010.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/978d/11510859/0d05f58e6d8f/toxins-16-00412-g001.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/978d/11510859/467b80d733ab/toxins-16-00412-g002.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/978d/11510859/6ea70da36d55/toxins-16-00412-g003.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/978d/11510859/3df96a19bdc4/toxins-16-00412-g004.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/978d/11510859/71f74c82b772/toxins-16-00412-g005.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/978d/11510859/06c07ad8c2f9/toxins-16-00412-g006.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/978d/11510859/357bd7f66084/toxins-16-00412-g007.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/978d/11510859/6a025b8c3672/toxins-16-00412-g008.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/978d/11510859/74c383447561/toxins-16-00412-g009.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/978d/11510859/70b9e685fbf8/toxins-16-00412-g010.jpg

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Biochemistry. 2024 Oct 1;63(19):2391-2396. doi: 10.1021/acs.biochem.4c00385. Epub 2024 Sep 19.
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Rapid detection of ricin at trace levels in complex matrices by asialofetuin-coated beads and bottom-up proteomics using high-resolution mass spectrometry.通过唾液酸结合胎球蛋白包被的珠体和使用高分辨率质谱的自上而下蛋白质组学,在复杂基质中痕量水平快速检测蓖麻毒素。
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Structural Basis of Antibody-Mediated Inhibition of Ricin Toxin Attachment to Host Cells.
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Biochemistry. 2023 Nov 21;62(22):3181-3187. doi: 10.1021/acs.biochem.3c00480. Epub 2023 Oct 30.
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Comparative Aspects of Ricin Toxicity by Inhalation.吸入蓖麻毒素的毒性比较。
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