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Related Experiment Videos

Antibody production.

John R Birch1, Andrew J Racher

  • 1Lonza Biologics plc, 228 Bath Road, Slough, Berkshire, SL1 4DX, UK. john.birch@lonza.com

Advanced Drug Delivery Reviews
|July 11, 2006
PubMed
Summary
This summary is machine-generated.

Monoclonal antibody production in mammalian cell culture has seen a 100-fold productivity increase due to improved expression and fed-batch processes. Future trends focus on faster cell line development for quicker clinical material production.

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Area of Science:

  • Biotechnology
  • Biopharmaceutical Manufacturing
  • Cell Culture Technology

Background:

  • The widespread clinical and commercial success of monoclonal antibodies necessitates large-scale production.
  • This has driven significant global expansion in manufacturing capacity, including larger bioreactors (up to 20,000 L).
  • There is a continuous effort to enhance process efficiency and reduce manufacturing costs.

Purpose of the Study:

  • To review current technologies for monoclonal antibody production, focusing on mammalian cell culture.
  • To discuss advancements in upstream processing, including expression technology and fed-batch cultures.
  • To explore future trends in monoclonal antibody manufacturing, particularly in accelerating process development and cell line creation.

Main Methods:

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  • Review of existing literature and industry practices in mammalian cell culture for monoclonal antibody production.
  • Analysis of improvements in expression technology and process optimization strategies.
  • Discussion of cell line development timelines and potential future innovations.
  • Main Results:

    • Upstream processing productivity has improved 100-fold over the last 15 years.
    • Improvements stem from enhanced expression systems and optimized fed-batch culture techniques.
    • Cell line creation remains a critical bottleneck in reducing overall process development time.

    Conclusions:

    • Mammalian cell culture is a cornerstone of modern monoclonal antibody manufacturing.
    • Significant progress has been made in upstream productivity, but cell line development requires further acceleration.
    • Future efforts will likely focus on streamlining early-stage development to expedite the availability of therapeutic materials.