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A novel glycosylated anti-CD20 monoclonal antibody from transgenic cattle
The monoclonal antibody (mAb) against CD20 known as Rituxan is widely used to treat autoimmune diseases and lymphomas. However, further application of Rituxan faces challenges of high production cost, which limits its availability in developing countries. Here, we report a new approach for large pro...
Autores principales: | , , , , , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Nature Publishing Group UK
2018
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6123398/ https://www.ncbi.nlm.nih.gov/pubmed/30181542 http://dx.doi.org/10.1038/s41598-018-31417-2 |
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author | Zhang, Ran Tang, Chenjun Guo, Huaizu Tang, Bo Hou, Sheng Zhao, Lei Wang, Jianwu Ding, Fangrong Zhao, Jianmin Wang, Haiping Chen, Zhongzhou Dai, Yunping Li, Ning |
author_facet | Zhang, Ran Tang, Chenjun Guo, Huaizu Tang, Bo Hou, Sheng Zhao, Lei Wang, Jianwu Ding, Fangrong Zhao, Jianmin Wang, Haiping Chen, Zhongzhou Dai, Yunping Li, Ning |
author_sort | Zhang, Ran |
collection | PubMed |
description | The monoclonal antibody (mAb) against CD20 known as Rituxan is widely used to treat autoimmune diseases and lymphomas. However, further application of Rituxan faces challenges of high production cost, which limits its availability in developing countries. Here, we report a new approach for large production of a recombinant anti-CD20 mAb in the milk of transgenic cattle (at a yield of up to ~6.8 mg/mL), with ~80% recovery rate and >99% purity. Crystallography study showed that our recombinant mAb is structurally nearly identical to Rituxan with only minor differences in N-linked glycosylation pattern. Functional study showed that, while our mAb shared similar target-cell binding capacities and complement-dependent cytotoxicity with Rituxan, our product exhibited a higher binding affinity for FcγRIIIα and a greater antibody-dependent cellular cytotoxicity. Accordingly, our recombinant mAb demonstrated a superior efficacy over Rituxan against B-cell lymphomas in severe combined immunodeficiency mice. Taken together, our data supports transgenic cattle as a novel model for cost-competitive, large-scale production of therapeutic antibodies. |
format | Online Article Text |
id | pubmed-6123398 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2018 |
publisher | Nature Publishing Group UK |
record_format | MEDLINE/PubMed |
spelling | pubmed-61233982018-09-10 A novel glycosylated anti-CD20 monoclonal antibody from transgenic cattle Zhang, Ran Tang, Chenjun Guo, Huaizu Tang, Bo Hou, Sheng Zhao, Lei Wang, Jianwu Ding, Fangrong Zhao, Jianmin Wang, Haiping Chen, Zhongzhou Dai, Yunping Li, Ning Sci Rep Article The monoclonal antibody (mAb) against CD20 known as Rituxan is widely used to treat autoimmune diseases and lymphomas. However, further application of Rituxan faces challenges of high production cost, which limits its availability in developing countries. Here, we report a new approach for large production of a recombinant anti-CD20 mAb in the milk of transgenic cattle (at a yield of up to ~6.8 mg/mL), with ~80% recovery rate and >99% purity. Crystallography study showed that our recombinant mAb is structurally nearly identical to Rituxan with only minor differences in N-linked glycosylation pattern. Functional study showed that, while our mAb shared similar target-cell binding capacities and complement-dependent cytotoxicity with Rituxan, our product exhibited a higher binding affinity for FcγRIIIα and a greater antibody-dependent cellular cytotoxicity. Accordingly, our recombinant mAb demonstrated a superior efficacy over Rituxan against B-cell lymphomas in severe combined immunodeficiency mice. Taken together, our data supports transgenic cattle as a novel model for cost-competitive, large-scale production of therapeutic antibodies. Nature Publishing Group UK 2018-09-04 /pmc/articles/PMC6123398/ /pubmed/30181542 http://dx.doi.org/10.1038/s41598-018-31417-2 Text en © The Author(s) 2018 Open Access This article is licensed under a Creative Commons Attribution 4.0 International License, which permits use, sharing, adaptation, distribution and reproduction in any medium or format, as long as you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons license, and indicate if changes were made. The images or other third party material in this article are included in the article’s Creative Commons license, unless indicated otherwise in a credit line to the material. If material is not included in the article’s Creative Commons license and your intended use is not permitted by statutory regulation or exceeds the permitted use, you will need to obtain permission directly from the copyright holder. To view a copy of this license, visit http://creativecommons.org/licenses/by/4.0/. |
spellingShingle | Article Zhang, Ran Tang, Chenjun Guo, Huaizu Tang, Bo Hou, Sheng Zhao, Lei Wang, Jianwu Ding, Fangrong Zhao, Jianmin Wang, Haiping Chen, Zhongzhou Dai, Yunping Li, Ning A novel glycosylated anti-CD20 monoclonal antibody from transgenic cattle |
title | A novel glycosylated anti-CD20 monoclonal antibody from transgenic cattle |
title_full | A novel glycosylated anti-CD20 monoclonal antibody from transgenic cattle |
title_fullStr | A novel glycosylated anti-CD20 monoclonal antibody from transgenic cattle |
title_full_unstemmed | A novel glycosylated anti-CD20 monoclonal antibody from transgenic cattle |
title_short | A novel glycosylated anti-CD20 monoclonal antibody from transgenic cattle |
title_sort | novel glycosylated anti-cd20 monoclonal antibody from transgenic cattle |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6123398/ https://www.ncbi.nlm.nih.gov/pubmed/30181542 http://dx.doi.org/10.1038/s41598-018-31417-2 |
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