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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...
Autores principales: | , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Public Library of Science
2018
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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. |
format | Online Article Text |
id | pubmed-5841786 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2018 |
publisher | Public Library of Science |
record_format | MEDLINE/PubMed |
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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