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Rapid and inexpensive purification of adenovirus vectors using an optimised aqueous two-phase technology.
Suleman, Saqlain; Schrubaji, Kuteiba; Filippou, Chrysovalanto; Ignatova, Svetlana; Hewitson, Peter; Huddleston, Jonathan; Karda, Rajvinder; Waddington, Simon N; Themis, Michael.
  • Suleman S; Division of Biosciences, Department of Life Sciences, College of Health, Medicine & Life Sciences, Brunel University London, Uxbridge, Middlesex, UK.
  • Schrubaji K; Division of Biosciences, Department of Life Sciences, College of Health, Medicine & Life Sciences, Brunel University London, Uxbridge, Middlesex, UK.
  • Filippou C; Division of Biosciences, Department of Life Sciences, College of Health, Medicine & Life Sciences, Brunel University London, Uxbridge, Middlesex, UK.
  • Ignatova S; Department of Chemical Engineering, College of Engineering, Design & Physical Sciences, Brunel University London, Uxbridge, Middlesex, UB8 3PH, UK.
  • Hewitson P; Department of Chemical Engineering, College of Engineering, Design & Physical Sciences, Brunel University London, Uxbridge, Middlesex, UB8 3PH, UK.
  • Huddleston J; Department of Chemical Engineering, College of Engineering, Design & Physical Sciences, Brunel University London, Uxbridge, Middlesex, UB8 3PH, UK.
  • Karda R; Gene Transfer Technology, EGA Institute for Women's Health, University College London, London, WC1E 6HX, UK.
  • Waddington SN; Gene Transfer Technology, EGA Institute for Women's Health, University College London, London, WC1E 6HX, UK; MRC Antiviral Gene Therapy Research Unit, Faculty of Health Sciences, University of the Witswatersrand, Johannesburg, South Africa.
  • Themis M; Division of Biosciences, Department of Life Sciences, College of Health, Medicine & Life Sciences, Brunel University London, Uxbridge, Middlesex, UK; Division of Ecology and Evolution, Department of Life Sciences, Imperial College London, London, SW7 2AZ, UK. Electronic address: michael.themis@b
J Virol Methods ; 299: 114305, 2022 01.
Article in English | MEDLINE | ID: covidwho-1458825
ABSTRACT
Adenoviruses (AdVs) are used as gene therapy vectors to treat human diseases and as vaccines against COVID-19. AdVs are produced by transfecting human embryonic kidney 239 (HEK293) or PER.C6 virus producer cells with AdV plasmid vectors or infecting these cells withcell lysates containing replication-defective AdV. Cell lysates can be purified further by caesium chloride or chromatographic protocols to research virus seed stocks (RVSS) for characterisation to high quality master virus seed stocks (MVSS) and working virus seed stocks (WVSS) before downstream production of pure, high titre AdV. Lysates are poorly infectious, block filtration columns and have limited storage capability. Aqueous two-phase systems (ATPS) are an alternative method for AdV purification that rapidly generates cleaner RVSS for characterisation to MVSS. After testing multiple ATPS formulations, an aqueous mixture of 20 % PEG 600 and 20 % (NH4)2SO4 (w/w) was found most effective for AdV partitioning, producing up to 97+3% yield of high-titre virus that was devoid of aggregates both effective in vitro and in vivo with no observable cytotoxicity. Importantly, AdV preparations stored at -20 °C or 4 °C show negligible loss of titre and are suitable for downstream processing to clinical grade to support the need for AdV vaccines.
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Full text: Available Collection: International databases Database: MEDLINE Main subject: COVID-19 Vaccines / COVID-19 Type of study: Prognostic study Topics: Vaccines Limits: Humans Language: English Journal: J Virol Methods Year: 2022 Document Type: Article Affiliation country: J.jviromet.2021.114305

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Full text: Available Collection: International databases Database: MEDLINE Main subject: COVID-19 Vaccines / COVID-19 Type of study: Prognostic study Topics: Vaccines Limits: Humans Language: English Journal: J Virol Methods Year: 2022 Document Type: Article Affiliation country: J.jviromet.2021.114305