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A nanowell platform to identify, sort and expand high antibody-producing cells.
Abali, Fikri; Schasfoort, Richard; Nijland, Sanne; Wittenberns, Jelle; Tibbe, Arjan G J; den Hartog, Marcel; Boon, Louis; Terstappen, Leon W M M.
Afiliação
  • Abali F; Department of Medical Cell BioPhysics, Faculty of Science and Technology, University of Twente, PO Box 217, 7500AE, Enschede, The Netherlands.
  • Schasfoort R; Department of Medical Cell BioPhysics, Faculty of Science and Technology, University of Twente, PO Box 217, 7500AE, Enschede, The Netherlands.
  • Nijland S; VYCAP, Capitool 41, 7521PL, Enschede, The Netherlands.
  • Wittenberns J; Polpharma Biologics Utrecht B.V., Yalelaan 46, 3584 CM, Utrecht, The Netherlands.
  • Tibbe AGJ; VYCAP, Capitool 41, 7521PL, Enschede, The Netherlands.
  • den Hartog M; Polpharma Biologics Utrecht B.V., Yalelaan 46, 3584 CM, Utrecht, The Netherlands.
  • Boon L; JJP Biologics, Bobrowiecka 6, 00-728, Warsaw, Poland.
  • Terstappen LWMM; Department of Medical Cell BioPhysics, Faculty of Science and Technology, University of Twente, PO Box 217, 7500AE, Enschede, The Netherlands. l.w.m.m.terstappen@utwente.nl.
Sci Rep ; 14(1): 9457, 2024 04 24.
Article em En | MEDLINE | ID: mdl-38658627
ABSTRACT
Increased use of therapeutic monoclonal antibodies and the relatively high manufacturing costs fuel the need for more efficient production methods. Here we introduce a novel, fast, robust, and safe isolation platform for screening and isolating antibody-producing cell lines using a nanowell chip and an innovative single-cell isolation method. An anti-Her2 antibody producing CHO cell pool was used as a model. The platform; (1) Assures the single-cell origin of the production clone, (2) Detects the antibody production of individual cells and (3) Isolates and expands the individual cells based on their antibody production. Using the nanowell platform we demonstrated an 1.8-4.5 increase in anti-Her2 production by CHO cells that were screened and isolated with the nanowell platform compared to CHO cells that were not screened. This increase was also shown in Fed-Batch cultures where selected high production clones showed titers of 19-100 mg/L on harvest day, while the low producer cells did not show any detectable anti-Her2 IgG production. The screening of thousands of single cells is performed under sterile conditions and the individual cells were cultured in buffers and reagents without animal components. The time required from seeding a single cell and measuring the antibody production to fully expanded clones with increased Her-2 production was 4-6 weeks.
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Texto completo: 1 Base de dados: MEDLINE Assunto principal: Cricetulus / Receptor ErbB-2 / Anticorpos Monoclonais Limite: Animals / Humans Idioma: En Ano de publicação: 2024 Tipo de documento: Article

Texto completo: 1 Base de dados: MEDLINE Assunto principal: Cricetulus / Receptor ErbB-2 / Anticorpos Monoclonais Limite: Animals / Humans Idioma: En Ano de publicação: 2024 Tipo de documento: Article