任建伟, 郑昕, 韩晓红. 腺相关病毒载体基因治疗药物生物分析技术及药代/药效动力学研究进展[J]. 罕见病研究, 2024, 3(3): 350-357. DOI: 10.12376/j.issn.2097-0501.2024.03.012
引用本文: 任建伟, 郑昕, 韩晓红. 腺相关病毒载体基因治疗药物生物分析技术及药代/药效动力学研究进展[J]. 罕见病研究, 2024, 3(3): 350-357. DOI: 10.12376/j.issn.2097-0501.2024.03.012
REN Jianwei, ZHENG Xin, HAN Xiaohong. Advances in Bioanalytical Techniques and Pharmacokinetics/Pharmacodynamics Research of Adeno-Associated Viral Vector Gene Therapy Drugs[J]. Journal of Rare Diseases, 2024, 3(3): 350-357. DOI: 10.12376/j.issn.2097-0501.2024.03.012
Citation: REN Jianwei, ZHENG Xin, HAN Xiaohong. Advances in Bioanalytical Techniques and Pharmacokinetics/Pharmacodynamics Research of Adeno-Associated Viral Vector Gene Therapy Drugs[J]. Journal of Rare Diseases, 2024, 3(3): 350-357. DOI: 10.12376/j.issn.2097-0501.2024.03.012

腺相关病毒载体基因治疗药物生物分析技术及药代/药效动力学研究进展

Advances in Bioanalytical Techniques and Pharmacokinetics/Pharmacodynamics Research of Adeno-Associated Viral Vector Gene Therapy Drugs

  • 摘要: 腺相关病毒(AAV)载体是近年来基因治疗领域的研究热点,由于其致病能力弱、免疫原性低、组织特异性强等特点,在基因治疗领域展现出了极大的潜力。AAV载体本质上为具有感染活性的病毒,其安全性和有效性需要新的生物分析技术来评估。目前,相关行业指南明确了对AAV载体生物分布、脱落、免疫原性等内容的评估需求,但对生物分析相关的要求却十分有限。本文从生物分布、脱落、免疫原性和药代动力学/药效动力学(PK/PD)研究4个方面对AAV载体基因治疗药物生物分析技术及PK/PD研究面临的挑战进行总结,以期为AAV载体基因治疗产品的临床研发提供参考。

     

    Abstract: Recently, adeno-associated virus(AAV)vectors have been a hotspot in gene therapy and have shown great potential for rare diseases therapy, due to their low pathogenicity, mild immunogenicity and high tissue specificity. The safety and efficacy of AAV vectors, which are essentially infectious viruses, require new bioanalytical techniques to assess. At present, the relevant industry guidelines have specified the needs for the assessment of biodistribution, shedding, and immunogenicity, but the requirements related to bioassay are limited. In this paper, we reviewed the bioanalytical techniques and pharmacokinetics/pharmacodynamics(PK/PD)research of AAV vectors and their challenges from four aspects: biodistribution, shedding, immunogenicity and PK/PD research, with the hope of providing some reference for the clinical development of AAV vectors gene therapy products.

     

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