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Assessment of the immunogenicity of residual host cell protein impurities of OsrHSA

Human serum albumin (HSA) is the most abundant protein in human plasma and is widely used at high doses for treating various diseases. Recombinant HSA is an alternative approach to plasma-derived HSA, providing increased safety and an unlimited supply. However, the safety of the residual host cell p...

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Autores principales: Abiri, Naghmeh, Pang, Jianlei, Ou, Jiquan, Shi, Bo, Wang, Xianghong, Zhang, Sucai, Sun, Yunxia, Yang, Daichang
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Public Library of Science 2018
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5841786/
https://www.ncbi.nlm.nih.gov/pubmed/29513721
http://dx.doi.org/10.1371/journal.pone.0193339
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author Abiri, Naghmeh
Pang, Jianlei
Ou, Jiquan
Shi, Bo
Wang, Xianghong
Zhang, Sucai
Sun, Yunxia
Yang, Daichang
author_facet Abiri, Naghmeh
Pang, Jianlei
Ou, Jiquan
Shi, Bo
Wang, Xianghong
Zhang, Sucai
Sun, Yunxia
Yang, Daichang
author_sort Abiri, Naghmeh
collection PubMed
description Human serum albumin (HSA) is the most abundant protein in human plasma and is widely used at high doses for treating various diseases. Recombinant HSA is an alternative approach to plasma-derived HSA, providing increased safety and an unlimited supply. However, the safety of the residual host cell proteins (HCPs) co-purified with Oryza sativa HSA (OsrHSA) remains to be determined. An animal system was used to assess the immunogenicity of OsrHSA and its residual HCPs. Low immunogenicity and immunotoxicity of the residual HCPs at a dose of 25 μg/kg, equivalent to 25 times the clinical dosage of HSA, were observed. An anti-drug-antibody (ADA) analysis revealed that anti-HSA, anti-OsrHSA or anti-HCP antibodies developed with a low frequency in pHSA and OsrHSA treatments, but the titers were as low as 1.0–2.0. Furthermore, the titer and the incidence of the specific antibodies were not significantly different between the pHSA and OsrHSA groups, indicating that OsrHSA presents similar immunogenicity to that of pHSA. More importantly, no cytokines were stimulated after the administration of OsrHSA and the residual HCPs, suggesting that there was no risk of a cytokine storm. These results demonstrated that the residual HCPs from OsrHSA have low immunogenicity, indicating that the rice endosperm is one of the best hosts for plant molecular pharming.
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spelling pubmed-58417862018-03-23 Assessment of the immunogenicity of residual host cell protein impurities of OsrHSA Abiri, Naghmeh Pang, Jianlei Ou, Jiquan Shi, Bo Wang, Xianghong Zhang, Sucai Sun, Yunxia Yang, Daichang PLoS One Research Article Human serum albumin (HSA) is the most abundant protein in human plasma and is widely used at high doses for treating various diseases. Recombinant HSA is an alternative approach to plasma-derived HSA, providing increased safety and an unlimited supply. However, the safety of the residual host cell proteins (HCPs) co-purified with Oryza sativa HSA (OsrHSA) remains to be determined. An animal system was used to assess the immunogenicity of OsrHSA and its residual HCPs. Low immunogenicity and immunotoxicity of the residual HCPs at a dose of 25 μg/kg, equivalent to 25 times the clinical dosage of HSA, were observed. An anti-drug-antibody (ADA) analysis revealed that anti-HSA, anti-OsrHSA or anti-HCP antibodies developed with a low frequency in pHSA and OsrHSA treatments, but the titers were as low as 1.0–2.0. Furthermore, the titer and the incidence of the specific antibodies were not significantly different between the pHSA and OsrHSA groups, indicating that OsrHSA presents similar immunogenicity to that of pHSA. More importantly, no cytokines were stimulated after the administration of OsrHSA and the residual HCPs, suggesting that there was no risk of a cytokine storm. These results demonstrated that the residual HCPs from OsrHSA have low immunogenicity, indicating that the rice endosperm is one of the best hosts for plant molecular pharming. Public Library of Science 2018-03-07 /pmc/articles/PMC5841786/ /pubmed/29513721 http://dx.doi.org/10.1371/journal.pone.0193339 Text en © 2018 Abiri et al http://creativecommons.org/licenses/by/4.0/ This is an open access article distributed under the terms of the Creative Commons Attribution License (http://creativecommons.org/licenses/by/4.0/) , which permits unrestricted use, distribution, and reproduction in any medium, provided the original author and source are credited.
spellingShingle Research Article
Abiri, Naghmeh
Pang, Jianlei
Ou, Jiquan
Shi, Bo
Wang, Xianghong
Zhang, Sucai
Sun, Yunxia
Yang, Daichang
Assessment of the immunogenicity of residual host cell protein impurities of OsrHSA
title Assessment of the immunogenicity of residual host cell protein impurities of OsrHSA
title_full Assessment of the immunogenicity of residual host cell protein impurities of OsrHSA
title_fullStr Assessment of the immunogenicity of residual host cell protein impurities of OsrHSA
title_full_unstemmed Assessment of the immunogenicity of residual host cell protein impurities of OsrHSA
title_short Assessment of the immunogenicity of residual host cell protein impurities of OsrHSA
title_sort assessment of the immunogenicity of residual host cell protein impurities of osrhsa
topic Research Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5841786/
https://www.ncbi.nlm.nih.gov/pubmed/29513721
http://dx.doi.org/10.1371/journal.pone.0193339
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