Effect of adenosine and cordycepin on recombinant antibody production yields in two different Chinease hamster ovary cell lines

  • Salinthip Jarusintanakorn
  • , Kuntalee Rangnoi
  • , Montarop Yamabhai*
  • , Enrico Mastrobattista*
  • *Corresponding author for this work

Research output: Contribution to journalArticleAcademicpeer-review

Abstract

In this study, we investigated the effect of adenosine and its derivative cordycepin on the production yield of a recombinant human monoclonal antibody (adalimumab) in two commonly used Chinese Hamster ovary (CHO) cell lines that have different gene amplification systems, namely CHO-DHFR - and GS-CHO knockout (GS-KO CHO) cells and that were grown in batch culture, with and without glucose feeding. The results showed that adenosine suppressed the cell growth rate and increased the fraction of cells in S phase of the cell cycle for both CHO cell lines. Different concentrations and exposure times of adenosine feeding were tested. The optimal yield of adalimumab production was achieved with the addition of 1 mM adenosine on day 2 after start of the batch culture. Adenosine could significantly improve antibody titers and productivity in both CHO cell lines in cultures without glucose feeding. However, upon glucose feeding, adenosine did not improve antibody titers in CHO-DHFR - cells but extended culture duration and significantly increased antibody titers in GS-KO CHO cells. Therefore, adenosine supplementation might be useful for antibody production in GS-KO CHO cells in medium- to large-scale batches. In case of cordycepin, a derivative of adenosine, CHO-DHFR - cells required higher concentration of cordycepin than GS-KO CHO cells around 10 times to display the changes in cell growth and cell cycle. Moreover, cordycepin could significantly increase antibody titers only in CHO-DHFR - cell cultures without glucose feeding.

Original languageEnglish
Article numbere3403
JournalBiotechnology Progress
Volume40
Issue number1
Early online date20 Nov 2023
DOIs
Publication statusPublished - Jan 2024

Bibliographical note

Publisher Copyright:
© 2023 The Authors. Biotechnology Progress published by Wiley Periodicals LLC on behalf of American Institute of Chemical Engineers.

Funding

SJ was financially supported by Mahidol University's Academic Development Scholarship. Cell culture experiments were financially supported by BIOTEC, National Science and Technology Development Agency (NSTDA) (grant number P-18-50127) and Ministry of Higher Education, Science, Research, and Innovation (MHESI) (grant number 256101A3040017) as well as Thailand Science Research and Innovation (TSRI) (TRF Senior Research grant number RTA6180012). MY was also supported by the Distinguished Research Professor Grant (NRCT 808/2563) of the National Research Council of Thailand.

FundersFunder number
Mahidol University
National Science and Technology Development AgencyP-18-50127
Thailand Research FundNRCT 808/2563, RTA6180012
National Research Council of Thailand
National Center for Genetic Engineering and Biotechnology
Ministry of Higher Education, Science, Research and Innovation, Thailand256101A3040017
Thailand Science Research and Innovation

    Keywords

    • CHO
    • adenosine
    • antibody titer
    • cell cycle arrest
    • cordycepin
    • productivity

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