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肿瘤学启发的 COVID-19 治疗选择。

Oncology-Inspired Treatment Options for COVID-19.

机构信息

Department of Radiology, Memorial Sloan Kettering Cancer Center, New York, New York.

Molecular Pharmacology Program, Memorial Sloan Kettering Cancer Center, New York, New York; and.

出版信息

J Nucl Med. 2020 Dec;61(12):1720-1723. doi: 10.2967/jnumed.120.249748. Epub 2020 Jul 17.

Abstract

CR3022 is a human antibody that binds to severe acute respiratory syndrome coronavirus 2 (SARS-CoV-2). Here, we explore the use of CR3022 as a molecularly targeted radiotherapeutic. CR3022 was labeled with I and purified, yielding I-CR3022. Using a magnetic bead assay and a recombinant SARS-CoV-2 spike protein fragment, we tested binding of I-CR3022 in the presence and absence of CR3022. We conjugated the antibody CR3022 with a purity of more than 98% and a specific activity of more than 292 MBq/mg. Using a bead-based assay, we confirmed that binding of I-CR3022 is selective and is significantly reduced in the presence of unlabeled antibody (3.14% ± 0.14% specific uptake and 0.10% ± 0.01% specific uptake, respectively; < 0.0001). Our results confirm the potential of CR3022 as a molecularly targeted probe for SARS-CoV-2. A labeled version of CR3022 could potentially be used for Auger radiotherapy or noninvasive imaging.

摘要

CR3022 是一种与人严重急性呼吸系统综合征冠状病毒 2(SARS-CoV-2)结合的抗体。在这里,我们探讨了将 CR3022 用作分子靶向放射疗法的用途。CR3022 用 I 进行标记并纯化,得到 I-CR3022。我们使用磁珠测定法和重组 SARS-CoV-2 刺突蛋白片段,测试了在存在和不存在 CR3022 的情况下 I-CR3022 的结合情况。我们将抗体 CR3022 与纯度超过 98%和比活度超过 292MBq/mg 的物质相缀合。使用基于珠的测定法,我们证实了 I-CR3022 的结合是选择性的,并且在存在未标记抗体时显著降低(分别为 3.14%±0.14%特异性摄取和 0.10%±0.01%特异性摄取;<0.0001)。我们的结果证实了 CR3022 作为 SARS-CoV-2 分子靶向探针的潜力。CR3022 的标记版本可能可用于 Auger 放疗或无创成像。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/fd09/8679628/e05ec4bffb7a/jnm249748fig1.jpg

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