When will we have a clone? An industry perspective on the typical CLD timeline.

CHO CLD Chinese hamster ovary biologics cell line development risk timeline

Journal

Biotechnology progress
ISSN: 1520-6033
Titre abrégé: Biotechnol Prog
Pays: United States
ID NLM: 8506292

Informations de publication

Date de publication:
13 Mar 2024
Historique:
revised: 07 02 2024
received: 01 12 2023
accepted: 14 02 2024
medline: 13 3 2024
pubmed: 13 3 2024
entrez: 13 3 2024
Statut: aheadofprint

Résumé

Cell line development (CLD) represents a complex but highly critical process during the development of a biological drug. To shed light on this crucial workflow, a team of BioPhorum members (authors) has developed and executed surveys focused on the activities and effort involved in a typical CLD campaign. An average of 27 members from different companies that participate in the BioPhorum CLD working group answered surveys covering three distinguishable stages of a standard CLD process: (1) Pre-transfection, including vector design and construction; (2) Transfection, spanning the initial introduction of vector into cells and subsequent selection and analysis of the pools; and (3) Single Cell Cloning and Lead Clone Selection, comprising methods of isolating single cells and confirming clonal origin, subsequent expansion and screening processes, and methods for identifying and banking lead clones. The surveys were very extensive, including a total of 341 questions split between antibody and complex molecule CLD processes. In this survey review, the authors interpret and highlight responses for antibody development and, where relevant, contrast complex molecule development challenges to provide a comprehensive industry perspective on the typical time and effort required to develop a CHO production cell line.

Identifiants

pubmed: 38477447
doi: 10.1002/btpr.3449
doi:

Types de publication

Journal Article Review

Langues

eng

Sous-ensembles de citation

IM

Pagination

e3449

Informations de copyright

© 2024 The Authors. Biotechnology Progress published by Wiley Periodicals LLC on behalf of American Institute of Chemical Engineers.

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Auteurs

Howard Clarke (H)

Seagen Inc., Cell Line Development, Bothell, Washington, USA.

Anke Mayer-Bartschmid (A)

Bayer AG, Biologics Development, Wuppertal, Germany.

Chenxing Zheng (C)

Incyte Corporation, Cell Line Development, Wilmington, Delaware, USA.

Elizabeth Masterjohn (E)

Sanofi, Cell Line Development, Framingham, Massachusetts, USA.

Falguni Patel (F)

AbbVie Inc., S&T Biologics Development & Launch, Worcester, Massachusetts, USA.

Mark Moffat (M)

Pfizer, Cell Line Development, Chesterfield, Missouri, USA.

Qingxiang Wei (Q)

Incyte Corporation, Cell Line Development, Wilmington, Delaware, USA.

Ren Liu (R)

Merck & Co., Inc., Process Cell Sciences, Rahway, New Jersey, USA.

Robyn Emmins (R)

GSK Medicines and Research Centre, Cell Line Development, Stevenage, UK.

Simon Fischer (S)

Boehringer Ingelheim Pharma GmbH & Co. KG, Cell Line Development, Biberach, Germany.

Stephanie Rieder (S)

AbbVie Inc., S&T Biologics Development & Launch, Worcester, Massachusetts, USA.

Thomas Kelly (T)

Janssen R&D, Cell Engineering & Analytical Sciences, Spring House, Pennsylvania, USA.

Classifications MeSH