LAPSE:2023.1104
Published Article

LAPSE:2023.1104
Identification of Cell Culture Factors Influencing Afucosylation Levels in Monoclonal Antibodies by Partial Least-Squares Regression and Variable Importance Metrics
February 21, 2023
Abstract
Retrospective analysis of historic data for cell culture processes is a powerful tool to develop further process understanding. In particular, deploying retrospective analyses can identify important cell culture process parameters for controlling critical quality attributes, e.g., afucosylation, for the production of monoclonal antibodies (mAbs). However, a challenge of analyzing large cell culture data is the high correlation between regressors (particularly media composition), which makes traditional analyses, such as analysis of variance and multivariate linear regression, inappropriate. Instead, partial least-squares regression (PLSR) models, in combination with machine learning techniques such as variable importance metrics, are an orthogonal or alternative approach to identifying important regressors and overcoming the challenge of a highly covariant data structure. A specific workflow for the retrospective analysis of cell culture data is proposed that covers data curation, PLS regression, model analysis, and further steps. In this study, the proposed workflow was applied to data from four mAb products in an industrial cell culture process to identify significant process parameters that influence the afucosylation levels. The PLSR workflow successfully identified several significant parameters, such as temperature and media composition, to enhance process understanding of the relationship between cell culture processes and afucosylation levels.
Retrospective analysis of historic data for cell culture processes is a powerful tool to develop further process understanding. In particular, deploying retrospective analyses can identify important cell culture process parameters for controlling critical quality attributes, e.g., afucosylation, for the production of monoclonal antibodies (mAbs). However, a challenge of analyzing large cell culture data is the high correlation between regressors (particularly media composition), which makes traditional analyses, such as analysis of variance and multivariate linear regression, inappropriate. Instead, partial least-squares regression (PLSR) models, in combination with machine learning techniques such as variable importance metrics, are an orthogonal or alternative approach to identifying important regressors and overcoming the challenge of a highly covariant data structure. A specific workflow for the retrospective analysis of cell culture data is proposed that covers data curation, PLS regression, model analysis, and further steps. In this study, the proposed workflow was applied to data from four mAb products in an industrial cell culture process to identify significant process parameters that influence the afucosylation levels. The PLSR workflow successfully identified several significant parameters, such as temperature and media composition, to enhance process understanding of the relationship between cell culture processes and afucosylation levels.
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Keywords
afucosylation, cell culture, monoclonal antibodies, partial least-squares regression (PLSR), selectivity ratio (SR), significance multivariate correlation (sMC), variable importance in projection (VIP) scores, variable importance metric
Subject
Suggested Citation
Rish AJ, Huang Z, Siddiquee K, Xu J, Anderson CA, Borys MC, Khetan A. Identification of Cell Culture Factors Influencing Afucosylation Levels in Monoclonal Antibodies by Partial Least-Squares Regression and Variable Importance Metrics. (2023). LAPSE:2023.1104
Author Affiliations
Rish AJ: Biologics Development, Global Product Development and Supply, Bristol Myers Squibb, Devens, MA 01434, USA; Graduate School for Pharmaceutical Sciences, Duquesne University, Pittsburgh, PA 15282, USA
Huang Z: Biologics Development, Global Product Development and Supply, Bristol Myers Squibb, Devens, MA 01434, USA [ORCID]
Siddiquee K: Biologics Development, Global Product Development and Supply, Bristol Myers Squibb, Devens, MA 01434, USA
Xu J: Biologics Development, Global Product Development and Supply, Bristol Myers Squibb, Devens, MA 01434, USA [ORCID]
Anderson CA: Graduate School for Pharmaceutical Sciences, Duquesne University, Pittsburgh, PA 15282, USA; Duquesne Center for Pharmaceutical Technology, Duquesne University, Pittsburgh, PA 15282, USA
Borys MC: Biologics Development, Global Product Development and Supply, Bristol Myers Squibb, Devens, MA 01434, USA
Khetan A: Biologics Development, Global Product Development and Supply, Bristol Myers Squibb, Devens, MA 01434, USA
Huang Z: Biologics Development, Global Product Development and Supply, Bristol Myers Squibb, Devens, MA 01434, USA [ORCID]
Siddiquee K: Biologics Development, Global Product Development and Supply, Bristol Myers Squibb, Devens, MA 01434, USA
Xu J: Biologics Development, Global Product Development and Supply, Bristol Myers Squibb, Devens, MA 01434, USA [ORCID]
Anderson CA: Graduate School for Pharmaceutical Sciences, Duquesne University, Pittsburgh, PA 15282, USA; Duquesne Center for Pharmaceutical Technology, Duquesne University, Pittsburgh, PA 15282, USA
Borys MC: Biologics Development, Global Product Development and Supply, Bristol Myers Squibb, Devens, MA 01434, USA
Khetan A: Biologics Development, Global Product Development and Supply, Bristol Myers Squibb, Devens, MA 01434, USA
Journal Name
Processes
Volume
11
Issue
1
First Page
223
Year
2023
Publication Date
2023-01-10
ISSN
2227-9717
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Original Submission
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PII: pr11010223, Publication Type: Journal Article
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LAPSE:2023.1104
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https://doi.org/10.3390/pr11010223
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Feb 21, 2023
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