将抗体药物共轭物作为病毒疗法潜在改良剂的临床策略

IF 6.5 2区 医学 Q1 PHARMACOLOGY & PHARMACY Drug Discovery Today Pub Date : 2024-09-11 DOI:10.1016/j.drudis.2024.104165
Zi-Xian Liao , Po-Hsiang Huang , Shan-hui Hsu , Hsiung-Hao Chang , Chi-Heng Chang , S.-Ja Tseng
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引用次数: 0

摘要

抗体-药物共轭物(ADCs)能够选择性地靶向癌细胞,因此是很有前景的治疗选择。在临床试验中,ADCs 已被用作肿瘤特异性细胞毒性有效载荷的载体,用于多种癌症的治疗。然而,溶瘤病毒疗法的全身给药具有挑战性,因为只有一小部分注射病毒能到达靶点。尽管批准了更高的病毒剂量,但大多数病毒最终仍会进入肝脏,可能对该器官造成毒性。以抗体-病毒共轭物或病毒-药物共轭物的形式将 ADC 与病毒疗法相结合,有可能克服这些挑战并改善治疗效果。
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Clinical strategies with antibody–drug conjugates as potential modifications for virotherapy

The ability to selectively target cancer cells makes antibody–drug conjugates (ADCs) promising therapeutic options. They have been tested in clinical trials as a vehicle for tumor-specific delivery of cytotoxic payloads for a range of cancers. However, systemic administration of oncolytic virotherapy is challenging, because only a small portion of injected viruses reach the target. Despite the approval of higher viral doses, most viruses still end up in the liver, potentially causing toxicity in that organ. Integrating ADCs with virotherapy in the form of antibody–virus conjugates or virus–drug conjugates can potentially overcome these challenges and improve therapeutic outcomes.

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来源期刊
Drug Discovery Today
Drug Discovery Today 医学-药学
CiteScore
14.80
自引率
2.70%
发文量
293
审稿时长
6 months
期刊介绍: Drug Discovery Today delivers informed and highly current reviews for the discovery community. The magazine addresses not only the rapid scientific developments in drug discovery associated technologies but also the management, commercial and regulatory issues that increasingly play a part in how R&D is planned, structured and executed. Features include comment by international experts, news and analysis of important developments, reviews of key scientific and strategic issues, overviews of recent progress in specific therapeutic areas and conference reports.
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