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Development of rapid and high sensitivity detection methods for replication-competent viruses contaminated in viral vector products for gene therapy

Development of rapid and high sensitivity detection methods for replication-competent viruses contaminated in viral vector products for gene therapy
开发用于基因治疗的病毒载体产品中污染的具有复制能力的病毒的快速、高灵敏度检测方法
批准号:
15590150
负责人:
UCHIDA Eriko
金额:
$2.3万
依托单位国家:
日本
项目类别:
Grant-in-Aid for Scientific Research (C)
财政年份:
2003
资助国家:
日本
项目状态:
已结题
起止时间:
2003 至 2004

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中文摘要
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英文摘要
Contamination by replication-competent viruses is one of the most important issues for safety and quality of virus vector products for gene therapy clinical research. In order to detect replication-competent adenovirus(RCA) and replication-competent retrovirus(RCR) contaminated in vector products more sensitively and rapidly, we have developed a novel detection method, a hybrid method that combines the infectivity assay and real-time quantitative(RT-) PCRInfectivity PCR was established for the detection of RCA. In this method, permissive cells were infected with RCA samples, and amplified RCA were quantified by real-time PCR. The glass-beads-based DNA extraction method was suitable for extracting DNA rapidly from RCA-infected cells. By infectivity PCR, 1 pfu of RCA spiked into 10^9 particles of adenovirus vectors could be detected within 3 days. In contrast, 1O^4 pfu of RCA could be detected by conventional cytopathic effect after 9 days of infection. These results showed that infectiv … More ity PCR was useful for the rapid and sensitive detection of RCA in adenovirus vector products.Infectivity RT-PCR was established for the detection of RCR. In this method, permissive cells were infected with RCR samples, and amplified RCR were quantified by real-time RT-PCR. Polyethyleneimine(PEI)-conjugated magnetic beads were used for concentration of RCR in the culture supernatants. By infectivity RT-PCR, 1 infectious unit(iu) of RCR spiked into 10^6 cfu/ml of retroviral vectors could be detected within 3 days. The sensitivity for viral detection was increased more than 10-fold compared with the conventional S+L- assay. Therefore, infectivity RT-PCR was useful for the rapid and sensitive detection of RCR in retrovirus vector products In addition, RCR could be detected more rapidly when RCR RNA were directly extracted from RCR-infected cells. Moreover, the infection efficiency and the detection sensitivity could be improved when PEI-magnetic beads and magnetic field were used for the infection of RCR. Less
期刊论文(18)
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会议论文
山口照英, 内田恵理子: "生物薬品のウイルス安全性を目的とした核酸増幅検査(NAT)のフィージビリティースタディー"医薬品研究. 34. 763-769 (2003)
Teruhide Yamaguchi、Eriko Uchida:“以生物药物病毒安全性为目的的核酸扩增测试 (NAT) 的可行性研究”Pharmaceutical Research 34. 763-769 (2003)。
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DOI: 10.1016/j.ymthe.2003.09.001
发表时间: 2003-12-01
期刊: MOLECULAR THERAPY
影响因子: 12.4
作者: [Ishii-Watabe, A, Uchida, E, Hayakawa, T]
通讯作者: Hayakawa, T
Ishii-Watabe A. et al.: "Detection of Replication-Competent Adenoviruses Spiked into Recombinant Adenovirus Vector Products by Infectivity-PCR Combined with Glass Beads-Based DNA Extraction."Molecular Therapy. 8. 1009-1016 (2003)
Ishii-Watabe A. 等人:“通过感染性 PCR 结合基于玻璃珠的 DNA 提取来检测掺入重组腺病毒载体产品中的具有复制能力的腺病毒。”分子治疗。
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An improved method for detection of replication competent retrovirus in retrovirus vector products
一种检测逆转录病毒载体产品中具有复制能力的逆转录病毒的改进方法
DOI: --
发表时间: 2004
期刊: Biologicals. 32
影响因子: --
作者: [Uchida E, Sato K., Iwata A., Ishii-Watabe A., Mizuguchi H., Hikata M., Murata M., Yamaguchi T., Hayakawa T.]
通讯作者: Hayakawa T.
Development of sensitive detection methods for viral shedding of adenovirus vector and replication-competent adenovirus
  • 批准号:
    17590141
  • 项目类别:
    Grant-in-Aid for Scientific Research (C)
  • 资助金额:
    $2.3万
  • 财政年份:
    2005
  • 负责人:
    UCHIDA Eriko
  • 依托单位:
海外基金