Literature DB >> 29855993

A new CHO (Chinese hamster ovary)-derived cell line expressing anti-TNFα monoclonal antibody with biosimilar potential.

Mateus Dalcin Luchese1, Mariana Lopes Dos Santos1, Angelica Garbuio1, Roselaine Campos Targino1, Carla Ploeger Mansueli1, Lilian Rumi Tsuruta1, Wagner Quintilio1, Ana Maria Moro2.   

Abstract

Tumor necrosis factor alpha (TNFα) 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-TNFα 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-TNFα 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 TNFα and FcRγ did not differ statistically when compared to reference adalimumab. One functional activity assay demonstrated the antibody neutralization capacity of the cytotoxicity induced by TNFα in L929 murine fibroblasts. A second assay confirmed adabut as an antagonist of the TNFα 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.

Entities:  

Keywords:  Autoimmunity; Biosimilar; CHO cells; Clone selection; ClonePix-FL; Monoclonal antibody; SPR; TNFα

Mesh:

Substances:

Year:  2018        PMID: 29855993     DOI: 10.1007/s12026-018-8997-4

Source DB:  PubMed          Journal:  Immunol Res        ISSN: 0257-277X            Impact factor:   2.829


  55 in total

1.  Comparison of humanized IgG and FvFc anti-CD3 monoclonal antibodies expressed in CHO cells.

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Journal:  Mol Biotechnol       Date:  2010-07       Impact factor: 2.695

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3.  Screening and subcloning of high producer transfectomas using semisolid media and automated colony picker.

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Journal:  Appl Microbiol Biotechnol       Date:  2016-09-27       Impact factor: 4.813

Review 5.  Anti-TNF therapy: past, present and future.

Authors:  Claudia Monaco; Jagdeep Nanchahal; Peter Taylor; Marc Feldmann
Journal:  Int Immunol       Date:  2014-11-19       Impact factor: 4.823

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7.  Dysregulated Fc receptor function in active rheumatoid arthritis.

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Journal:  Immunol Lett       Date:  2014-09-04       Impact factor: 3.685

8.  Transgenic mice expressing human tumour necrosis factor: a predictive genetic model of arthritis.

Authors:  J Keffer; L Probert; H Cazlaris; S Georgopoulos; E Kaslaris; D Kioussis; G Kollias
Journal:  EMBO J       Date:  1991-12       Impact factor: 11.598

9.  Cryopreservation of human vascular umbilical cord cells under good manufacturing practice conditions for future cell banks.

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Journal:  J Transl Med       Date:  2012-05-16       Impact factor: 5.531

Review 10.  Biosimilars advancements: Moving on to the future.

Authors:  Lilian Rumi Tsuruta; Mariana Lopes dos Santos; Ana Maria Moro
Journal:  Biotechnol Prog       Date:  2015-03-16
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2.  Functional production of human antibody by the filamentous fungus Aspergillus oryzae.

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