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In vitro and in vivo studies of plant-produced Atezolizumab as a potential immunotherapeutic antibody

Immune checkpoint inhibitors are a well-known class of immunotherapeutic drugs that have been used for effective treatment of several cancers. Atezolizumab (Tecentriq) was the first antibody to target immune checkpoint PD-L1 and is now among the most commonly used anticancer therapies. However, this...

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Autores principales: Rattanapisit, Kaewta, Bulaon, Christine Joy I., Strasser, Richard, Sun, Hongyan, Phoolcharoen, Waranyoo
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Nature Publishing Group UK 2023
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10465495/
https://www.ncbi.nlm.nih.gov/pubmed/37644118
http://dx.doi.org/10.1038/s41598-023-41510-w
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author Rattanapisit, Kaewta
Bulaon, Christine Joy I.
Strasser, Richard
Sun, Hongyan
Phoolcharoen, Waranyoo
author_facet Rattanapisit, Kaewta
Bulaon, Christine Joy I.
Strasser, Richard
Sun, Hongyan
Phoolcharoen, Waranyoo
author_sort Rattanapisit, Kaewta
collection PubMed
description Immune checkpoint inhibitors are a well-known class of immunotherapeutic drugs that have been used for effective treatment of several cancers. Atezolizumab (Tecentriq) was the first antibody to target immune checkpoint PD-L1 and is now among the most commonly used anticancer therapies. However, this anti-PD-L1 antibody is produced in mammalian cells with high manufacturing costs, limiting cancer patients’ access to the antibody treatment. Plant expression system is another platform that can be utilized, as they can synthesize complex glycoproteins, are rapidly scalable, and relatively cost-efficient. Herein, Atezolizumab was transiently produced in Nicotiana benthamiana and demonstrated high expression level within 4–6 days post-infiltration. After purification by affinity chromatography, the purified plant-produced Atezolizumab was compared to Tecentriq and showed the absence of glycosylation. Furthermore, the plant-produced Atezolizumab could bind to PD-L1 with comparable affinity to Tecentriq in ELISA. The tumor growth inhibitory activity of plant-produced Atezolizumab in mice was also found to be similar to that of Tecentriq. These findings confirm the plant’s capability to serve as an efficient production platform for immunotherapeutic antibodies and suggest that it could be used to alleviate the cost of existing anticancer products.
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spelling pubmed-104654952023-08-31 In vitro and in vivo studies of plant-produced Atezolizumab as a potential immunotherapeutic antibody Rattanapisit, Kaewta Bulaon, Christine Joy I. Strasser, Richard Sun, Hongyan Phoolcharoen, Waranyoo Sci Rep Article Immune checkpoint inhibitors are a well-known class of immunotherapeutic drugs that have been used for effective treatment of several cancers. Atezolizumab (Tecentriq) was the first antibody to target immune checkpoint PD-L1 and is now among the most commonly used anticancer therapies. However, this anti-PD-L1 antibody is produced in mammalian cells with high manufacturing costs, limiting cancer patients’ access to the antibody treatment. Plant expression system is another platform that can be utilized, as they can synthesize complex glycoproteins, are rapidly scalable, and relatively cost-efficient. Herein, Atezolizumab was transiently produced in Nicotiana benthamiana and demonstrated high expression level within 4–6 days post-infiltration. After purification by affinity chromatography, the purified plant-produced Atezolizumab was compared to Tecentriq and showed the absence of glycosylation. Furthermore, the plant-produced Atezolizumab could bind to PD-L1 with comparable affinity to Tecentriq in ELISA. The tumor growth inhibitory activity of plant-produced Atezolizumab in mice was also found to be similar to that of Tecentriq. These findings confirm the plant’s capability to serve as an efficient production platform for immunotherapeutic antibodies and suggest that it could be used to alleviate the cost of existing anticancer products. Nature Publishing Group UK 2023-08-29 /pmc/articles/PMC10465495/ /pubmed/37644118 http://dx.doi.org/10.1038/s41598-023-41510-w Text en © The Author(s) 2023 https://creativecommons.org/licenses/by/4.0/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 licence, and indicate if changes were made. The images or other third party material in this article are included in the article's Creative Commons licence, unless indicated otherwise in a credit line to the material. If material is not included in the article's Creative Commons licence 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 licence, visit http://creativecommons.org/licenses/by/4.0/ (https://creativecommons.org/licenses/by/4.0/) .
spellingShingle Article
Rattanapisit, Kaewta
Bulaon, Christine Joy I.
Strasser, Richard
Sun, Hongyan
Phoolcharoen, Waranyoo
In vitro and in vivo studies of plant-produced Atezolizumab as a potential immunotherapeutic antibody
title In vitro and in vivo studies of plant-produced Atezolizumab as a potential immunotherapeutic antibody
title_full In vitro and in vivo studies of plant-produced Atezolizumab as a potential immunotherapeutic antibody
title_fullStr In vitro and in vivo studies of plant-produced Atezolizumab as a potential immunotherapeutic antibody
title_full_unstemmed In vitro and in vivo studies of plant-produced Atezolizumab as a potential immunotherapeutic antibody
title_short In vitro and in vivo studies of plant-produced Atezolizumab as a potential immunotherapeutic antibody
title_sort in vitro and in vivo studies of plant-produced atezolizumab as a potential immunotherapeutic antibody
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10465495/
https://www.ncbi.nlm.nih.gov/pubmed/37644118
http://dx.doi.org/10.1038/s41598-023-41510-w
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