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A new CHO (Chinese hamster ovary)-derived cell line expressing anti-TNFa monoclonal antibody with biosimilar potential
Luchese, Mateus Dalcin; Lopes dos Santos, Mariana; Garbuio, Angelica; Targino, Roselaine Campos; Mansueli, Carla Ploeger; Tsuruta, Lilian Rumi; Quintilio, Wagner; Moro, Ana Maria.
Affiliation
  • Luchese, Mateus Dalcin; Instituto Butantan. Laboratório Especial de Biofármacos em Células Animais.
  • Lopes dos Santos, Mariana; Instituto Butantan. Laboratório Especial de Biofármacos em Células Animais.
  • Garbuio, Angelica; Instituto Butantan. Laboratório Especial de Biofármacos em Células Animais.
  • Targino, Roselaine Campos; Instituto Butantan. Laboratório Especial de Biofármacos em Células Animais.
  • Mansueli, Carla Ploeger; Instituto Butantan. Laboratório Especial de Biofármacos em Células Animais.
  • Tsuruta, Lilian Rumi; Instituto Butantan. Laboratório Especial de Biofármacos em Células Animais.
  • Quintilio, Wagner; Instituto Butantan. Laboratório Especial de Biofármacos em Células Animais.
  • Moro, Ana Maria; Instituto Butantan. Laboratório Especial de Biofármacos em Células Animais.
Immunol. Res. ; 66(3): p. 392-405, 2018.
Article in English | Sec. Est. Saúde SP, SESSP-IBPROD, Sec. Est. Saúde SP | ID: but-ib15234
Responsible library: BR78.1
Localization: BR78.1
ABSTRACT
Tumor necrosis factor alpha (TNF alpha) is a pro-inflammatory cytokine that mediates the homeostasis of immune responses; its exacerbated production is associated with the pathogenesis of autoimmune and chronic inflammatory diseases. Anti-TNF alpha drugs have revolutionized the treatment of inflammatory conditions such as rheumatoid arthritis and Crohn's disease. Currently, a worldwide race is on stage for the production of biosimilars moved by patent expiration of monoclonal antibodies (mAbs), such as anti-TNF alpha adalimumab. Our goal was to develop the first stage of an adalimumab biosimilar candidate with potential for national production, through the generation of a productive and stable cell line and assess its functionality. The robotic system ClonePix was used for screening and isolation of colonies from transfected CHO-S stable pools plated in semisolid medium. Selected clones were expanded based on growth and productivity. Purified mAbs from different clones were tested for binding and functional activity. The binding affinity of the denominated adabut clones to TNF alpha and FcR gamma did not differ statistically when compared to reference adalimumab. One functional activity assay demonstrated the antibody neutralization capacity of the cytotoxicity induced by TNF alpha in L929 murine fibroblasts. A second assay confirmed adabut as an antagonist of the TNF alpha activity by the inhibition of the cell adhesion molecule expression in HUVEC cultures. The binding and functional activity analyses performed with selected adabut clones in comparison to reference adalimumab represent an important status of "non-inferiority," part of the process required for a biosimilar development. We generated and selected high-quality adabut clones which mAbs may be further developed as the first in-house made Brazilian biosimilar, demonstrating a success case for our incipient biotechnology industry, or also modified as biobetters, thus representing an innovative strategy for the patients' welfare.
Full text: Available Collection: National databases / Brazil Database: Sec. Est. Saúde SP / SESSP-IBPROD Language: English Journal: Immunol. Res. Year: 2018 Document type: Article
Full text: Available Collection: National databases / Brazil Database: Sec. Est. Saúde SP / SESSP-IBPROD Language: English Journal: Immunol. Res. Year: 2018 Document type: Article
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