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Establishment of virus-free cell substrates for protein drug production

Research Project

Project/Area Number 18K07853
Research Category

Grant-in-Aid for Scientific Research (C)

Allocation TypeMulti-year Fund
Section一般
Review Section Basic Section 52050:Embryonic medicine and pediatrics-related
Research InstitutionJichi Medical University

Principal Investigator

Kume Akihiro  自治医科大学, 医学部, 教授 (10264293)

Project Period (FY) 2018-04-01 – 2021-03-31
Project Status Completed (Fiscal Year 2020)
Budget Amount *help
¥4,420,000 (Direct Cost: ¥3,400,000、Indirect Cost: ¥1,020,000)
Fiscal Year 2020: ¥1,300,000 (Direct Cost: ¥1,000,000、Indirect Cost: ¥300,000)
Fiscal Year 2019: ¥1,300,000 (Direct Cost: ¥1,000,000、Indirect Cost: ¥300,000)
Fiscal Year 2018: ¥1,820,000 (Direct Cost: ¥1,400,000、Indirect Cost: ¥420,000)
Keywordsバイオ医薬品 / 細胞基材 / ウイルス汚染 / 細胞基質 / 内在性ウイルス
Outline of Final Research Achievements

The current mainstream of novel drug discovery is rapidly changing from small molecules to biotechnologically produced proteins such as monoclonal antibodies. To produce recombinant proteins, insect cell lines such as Sf9 and High Five have been increasingly favored cell substrates because of their superb efficiency. Recently, however, novel viruses have been discovered as persistent infectants of these cell lines, e.g., SfRV rhabdovirus on Sf9 and TnNV nodavirus on High Five. These findings brought safety concerns on the protein drugs produced with present cell substrates, therefore establishing virus-free insect cells is an urgent issue. Through this study, the researcher successfully removed SfRV from Mimic Sf9, a derivative of Sf9 cells, and established rhabdovirus-free cell lines. The result will aid safer production of recombinant protein drugs for human use.

Academic Significance and Societal Importance of the Research Achievements

医薬品、特にバイオ医薬品の安全性において、原材料から混入しうるウイルスやプリオンなどの感染性因子の問題は常に問題となる重大関心事である。Sf9に感染しているSfRVやHigh Fiveに感染しているTnNVについては、ヒトを含めた哺乳類に対する病原性は知られておらず、ICH-Q5ガイドラインでは「ケースC」として医薬品製造工程で十分なウイルスクリアランスを示せばよいことになっているが、工程内除去はあくまで相対的なものであり、根本的解決とは言い切れない。本課題の成果として得られたウイルスフリー細胞株は、そのような要求に対する答えの一つである。

Report

(4 results)
  • 2020 Annual Research Report   Final Research Report ( PDF )
  • 2019 Research-status Report
  • 2018 Research-status Report
  • Research Products

    (4 results)

All 2020 2019 2018

All Journal Article (2 results) (of which Peer Reviewed: 2 results,  Open Access: 1 results) Presentation (1 results) (of which Int'l Joint Research: 1 results) Book (1 results)

  • [Journal Article] Aspects of Gene Therapy Products Using Current Genome-Editing Technology in Japan2020

    • Author(s)
      Yamaguchi Teruhide、Uchida Eriko、Okada Takashi、Ozawa Keiya、Onodera Masafumi、Kume Akihiro、Shimada Takashi、Takahashi Satoru、Tani Kenzaburo、Nasu Yasutomo、Mashimo Tomoji、Mizuguchi Hiroyuki、Mitani Kohnosuke、Maki Kazushige
    • Journal Title

      Human Gene Therapy

      Volume: 31 Issue: 19-20 Pages: 1043-1053

    • DOI

      10.1089/hum.2020.156

    • NAID

      120007147867

    • Related Report
      2020 Annual Research Report
    • Peer Reviewed / Open Access
  • [Journal Article] AAV6-mediated IL-10 expression in the lung ameliorates bleomycin-induced pulmonary fibrosis.2018

    • Author(s)
      Kurosaki F, Uchibori R, Mato N, Sehara Y, SagaY, Urabe M, Mizukami H, Sugiyama Y, Kume A
    • Journal Title

      Human Gene Therapy

      Volume: 29 Pages: 1242-1251

    • Related Report
      2018 Research-status Report
    • Peer Reviewed
  • [Presentation] Adenoassociated virus (AAV) serotype 3-based vector as an alternative vehicle for liver-directed gene therapy2019

    • Author(s)
      Kume A, Muramatsu S, Mizukami H, Onmori T
    • Organizer
      European Society of Gene and Cell Therapy
    • Related Report
      2019 Research-status Report
    • Int'l Joint Research
  • [Book] バイオ医薬品・再生医療等製品開発のためのカルタヘナ法2018

    • Author(s)
      久米 晃啓
    • Total Pages
      121
    • Publisher
      サイエンス&テクノロジー
    • ISBN
      9784864281775
    • Related Report
      2018 Research-status Report

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Published: 2018-04-23   Modified: 2022-01-27  

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