New Cell Lines Produce an Antibody Key for Biologic Drug Production
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When the National Institute of Standards and Technology (NIST) issued the world’s first standardized monoclonal antibody (mAb) in July 2016, the exhaustively analyzed protein known as NISTmAb (NIST Reference Material 8671) was intended as a valuable tool for biopharmaceutical companies.
Its purpose: to help ensure the quality of measurement techniques used in the development and manufacture of biologic drug therapies for a wide range of health conditions, including cancers, autoimmune disorders and infectious diseases.
Although the molecule has been precisely characterized, the current proprietary method for its production has not.
In a new paper in the journal mAbs, researchers at the Institute for Bioscience and Biotechnology Research (IBBR), a joint institute of NIST and the University of Maryland, describe how they have taken the first step to solve this dilemma: engineering three mouse cell lines to produce nonproprietary versions of NISTmAb that closely resemble the characteristics of the original reference material.
“By creating the means to produce our already well-characterized monoclonal antibody, the NISTmAb, we can now make the measurements that will define the production process as well as the product,” said NIST research biologist Zvi Kelman who co-authored the mAbs paper. “From that, we can develop a standardized model for monoclonal antibody biomanufacturing that will give researchers and manufacturers a second valuable reference tool.”
Monoclonal antibodies are proteins manufactured in the laboratory that can target specific disease cells, viruses and other antigens (agents that trigger an immune response) for removal from the body or can be used to deliver therapeutic chemicals or radiation to select sites. Since the first commercial mAb was approved in 1986, their impact on medicine has been astounding. Today, five of the 10 top-selling drugs are mAbs with annual sales currently at $100 billion and expected to rise to $150 billion within three years.
As the patents on the original mAb biologics expire or near expiration over the next few years, many biopharmaceutical companies will seek to enter the market with generic versions known as biosimilars.
“Both the manufacturers seeking legal and public approval for their biosimilars and regulators at the Food and Drug Administration must verify that the new drugs match the originals with regard to efficacy, quality and safety,” said John Marino, leader of the Biomolecular Structure and Function Group in NIST’s Material Measurement Laboratory and another author on the mAbs paper. “Having a rigorously characterized mAb production process, along with our standard NISTmAb protein, will serve as powerful benchmarking tools that should help manufacturers and regulators release new mAb therapeutics and biosimilars with greater confidence.”
Quality control is not the only way that the NISTmAb cell lines will make a difference, Marino added.
“Understanding how the NISTmAb is derived will enable investigators to look for ways to optimize the production of other mAbs or overcome commonly shared problems such as contamination or aggregation [protein clumping],” he said.
Equally important, Kelman said, the knowledge and benefits gained from study of the nonproprietary NISTmAb bioprocessing system will be freely available and widely shared.
“Researchers will be able to look at the broad issues currently facing manufacturers of mAb therapeutics with a system that is not proprietary; the NIST cell lines will encourage innovation and exploration that isn’t related to specific product development,” he explained.
This article has been republished from materials provided by the National Institute of Standards and Technology (USA). Note: material may have been edited for length and content. For further information, please contact the cited source.
Kashi, L., Yandrofski, K., Preston, R. J., Arbogast, L. W., Giddens, J. P., Marino, J. P., . . . Kelman, Z. (2018). Heterologous recombinant expression of non-originator NISTmAb. MAbs, 1-12. doi:10.1080/19420862.2018.1486355