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Immunogenicity of glycans on biotherapeutic drugs produced in plant expression systems—The taliglucerase alfa story
Plants are a promising alternative for the production of biotherapeutics. Manufacturing in-planta adds plant specific glycans. To understand immunogenic potential of these glycans, we developed a validated method to detect plant specific glycan antibodies in human serum. Using this assay, low preval...
Autores principales: | , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Public Library of Science
2017
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5663370/ https://www.ncbi.nlm.nih.gov/pubmed/29088235 http://dx.doi.org/10.1371/journal.pone.0186211 |
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author | Rup, Bonita Alon, Sari Amit-Cohen, Bat-Chen Brill Almon, Einat Chertkoff, Raul Tekoah, Yoram Rudd, Pauline M. |
author_facet | Rup, Bonita Alon, Sari Amit-Cohen, Bat-Chen Brill Almon, Einat Chertkoff, Raul Tekoah, Yoram Rudd, Pauline M. |
author_sort | Rup, Bonita |
collection | PubMed |
description | Plants are a promising alternative for the production of biotherapeutics. Manufacturing in-planta adds plant specific glycans. To understand immunogenic potential of these glycans, we developed a validated method to detect plant specific glycan antibodies in human serum. Using this assay, low prevalence of pre-existing anti-plant glycan antibodies was found in healthy humans (13.5%) and in glucocerebrosidase-deficient Gaucher disease (GD) patients (5%). A low incidence (9% in naïve patient and none in treatment experienced patients) of induced anti-plant glycan antibodies was observed in GD patients after up to 30 months replacement therapy treatment with taliglucerase alfa, a version of human glucocerebrosidase produced in plant cells. Detailed evaluation of clinical safety and efficacy endpoints indicated that anti-plant glycan antibodies did not affect the safety or efficacy of taliglucerase alfa in patients. This study shows the benefit of using large scale human trials to evaluate the immunogenicity risk of plant derived glycans, and indicates no apparent risk related to anti-plant glycan antibodies. |
format | Online Article Text |
id | pubmed-5663370 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2017 |
publisher | Public Library of Science |
record_format | MEDLINE/PubMed |
spelling | pubmed-56633702017-11-09 Immunogenicity of glycans on biotherapeutic drugs produced in plant expression systems—The taliglucerase alfa story Rup, Bonita Alon, Sari Amit-Cohen, Bat-Chen Brill Almon, Einat Chertkoff, Raul Tekoah, Yoram Rudd, Pauline M. PLoS One Research Article Plants are a promising alternative for the production of biotherapeutics. Manufacturing in-planta adds plant specific glycans. To understand immunogenic potential of these glycans, we developed a validated method to detect plant specific glycan antibodies in human serum. Using this assay, low prevalence of pre-existing anti-plant glycan antibodies was found in healthy humans (13.5%) and in glucocerebrosidase-deficient Gaucher disease (GD) patients (5%). A low incidence (9% in naïve patient and none in treatment experienced patients) of induced anti-plant glycan antibodies was observed in GD patients after up to 30 months replacement therapy treatment with taliglucerase alfa, a version of human glucocerebrosidase produced in plant cells. Detailed evaluation of clinical safety and efficacy endpoints indicated that anti-plant glycan antibodies did not affect the safety or efficacy of taliglucerase alfa in patients. This study shows the benefit of using large scale human trials to evaluate the immunogenicity risk of plant derived glycans, and indicates no apparent risk related to anti-plant glycan antibodies. Public Library of Science 2017-10-31 /pmc/articles/PMC5663370/ /pubmed/29088235 http://dx.doi.org/10.1371/journal.pone.0186211 Text en © 2017 Rup 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 Rup, Bonita Alon, Sari Amit-Cohen, Bat-Chen Brill Almon, Einat Chertkoff, Raul Tekoah, Yoram Rudd, Pauline M. Immunogenicity of glycans on biotherapeutic drugs produced in plant expression systems—The taliglucerase alfa story |
title | Immunogenicity of glycans on biotherapeutic drugs produced in plant expression systems—The taliglucerase alfa story |
title_full | Immunogenicity of glycans on biotherapeutic drugs produced in plant expression systems—The taliglucerase alfa story |
title_fullStr | Immunogenicity of glycans on biotherapeutic drugs produced in plant expression systems—The taliglucerase alfa story |
title_full_unstemmed | Immunogenicity of glycans on biotherapeutic drugs produced in plant expression systems—The taliglucerase alfa story |
title_short | Immunogenicity of glycans on biotherapeutic drugs produced in plant expression systems—The taliglucerase alfa story |
title_sort | immunogenicity of glycans on biotherapeutic drugs produced in plant expression systems—the taliglucerase alfa story |
topic | Research Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5663370/ https://www.ncbi.nlm.nih.gov/pubmed/29088235 http://dx.doi.org/10.1371/journal.pone.0186211 |
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