Cargando…

New Alternatives for Autoimmune Disease Treatments: Physicochemical and Clinical Comparability of Biosimilar Etanercept

Etanercept is a recombinant fusion protein approved for the treatment of TNF-α mediated diseases such as rheumatoid arthritis (RA), psoriasis, psoriatic arthritis, and ankylosing spondylitis. Herein, we present an evaluation of the physicochemical and biological properties of a biosimilar etanercept...

Descripción completa

Detalles Bibliográficos
Autores principales: Miranda-Hernández, Mariana P., López-Morales, Carlos A., Perdomo-Abúndez, Francisco C., Salazar-Flores, Rodolfo D., Ramírez-Ibanez, Nancy D., Pérez, Nestor O., Molina-Pérez, Aarón, Revilla-Beltri, Jorge, Flores-Ortiz, Luis F., Medina-Rivero, Emilio
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Hindawi Publishing Corporation 2016
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4921158/
https://www.ncbi.nlm.nih.gov/pubmed/27382576
http://dx.doi.org/10.1155/2016/9697080
_version_ 1782439485772922880
author Miranda-Hernández, Mariana P.
López-Morales, Carlos A.
Perdomo-Abúndez, Francisco C.
Salazar-Flores, Rodolfo D.
Ramírez-Ibanez, Nancy D.
Pérez, Nestor O.
Molina-Pérez, Aarón
Revilla-Beltri, Jorge
Flores-Ortiz, Luis F.
Medina-Rivero, Emilio
author_facet Miranda-Hernández, Mariana P.
López-Morales, Carlos A.
Perdomo-Abúndez, Francisco C.
Salazar-Flores, Rodolfo D.
Ramírez-Ibanez, Nancy D.
Pérez, Nestor O.
Molina-Pérez, Aarón
Revilla-Beltri, Jorge
Flores-Ortiz, Luis F.
Medina-Rivero, Emilio
author_sort Miranda-Hernández, Mariana P.
collection PubMed
description Etanercept is a recombinant fusion protein approved for the treatment of TNF-α mediated diseases such as rheumatoid arthritis (RA), psoriasis, psoriatic arthritis, and ankylosing spondylitis. Herein, we present an evaluation of the physicochemical and biological properties of a biosimilar etanercept and its reference product followed by a clinical study in patients diagnosed with RA intended to demonstrate comparability of their immunomodulatory activity. Identity analyses showed a total correspondence of the primary and higher-order structure between the two products. In regard to intrinsic heterogeneity, both products showed to be highly heterogenous; however the biosimilar etanercept exhibited similar charge and glycan heterogeneity intervals compared to the reference product. Apoptosis inhibition assay also showed that, despite the high degree of heterogeneity exhibited by both products, no significant differences exist in their in vitro activity. Finally, the clinical assessment conducted in RA-diagnosed patients did not show significant differences in the evaluated pharmacodynamic markers of both products. Collectively, the results from the comparability exercise provide convincing evidence that the evaluated biosimilar etanercept can be considered an effective alternative for the treatment of RA.
format Online
Article
Text
id pubmed-4921158
institution National Center for Biotechnology Information
language English
publishDate 2016
publisher Hindawi Publishing Corporation
record_format MEDLINE/PubMed
spelling pubmed-49211582016-07-05 New Alternatives for Autoimmune Disease Treatments: Physicochemical and Clinical Comparability of Biosimilar Etanercept Miranda-Hernández, Mariana P. López-Morales, Carlos A. Perdomo-Abúndez, Francisco C. Salazar-Flores, Rodolfo D. Ramírez-Ibanez, Nancy D. Pérez, Nestor O. Molina-Pérez, Aarón Revilla-Beltri, Jorge Flores-Ortiz, Luis F. Medina-Rivero, Emilio J Immunol Res Clinical Study Etanercept is a recombinant fusion protein approved for the treatment of TNF-α mediated diseases such as rheumatoid arthritis (RA), psoriasis, psoriatic arthritis, and ankylosing spondylitis. Herein, we present an evaluation of the physicochemical and biological properties of a biosimilar etanercept and its reference product followed by a clinical study in patients diagnosed with RA intended to demonstrate comparability of their immunomodulatory activity. Identity analyses showed a total correspondence of the primary and higher-order structure between the two products. In regard to intrinsic heterogeneity, both products showed to be highly heterogenous; however the biosimilar etanercept exhibited similar charge and glycan heterogeneity intervals compared to the reference product. Apoptosis inhibition assay also showed that, despite the high degree of heterogeneity exhibited by both products, no significant differences exist in their in vitro activity. Finally, the clinical assessment conducted in RA-diagnosed patients did not show significant differences in the evaluated pharmacodynamic markers of both products. Collectively, the results from the comparability exercise provide convincing evidence that the evaluated biosimilar etanercept can be considered an effective alternative for the treatment of RA. Hindawi Publishing Corporation 2016 2016-06-12 /pmc/articles/PMC4921158/ /pubmed/27382576 http://dx.doi.org/10.1155/2016/9697080 Text en Copyright © 2016 Mariana P. Miranda-Hernández et al. https://creativecommons.org/licenses/by/4.0/ This is an open access article distributed under the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited.
spellingShingle Clinical Study
Miranda-Hernández, Mariana P.
López-Morales, Carlos A.
Perdomo-Abúndez, Francisco C.
Salazar-Flores, Rodolfo D.
Ramírez-Ibanez, Nancy D.
Pérez, Nestor O.
Molina-Pérez, Aarón
Revilla-Beltri, Jorge
Flores-Ortiz, Luis F.
Medina-Rivero, Emilio
New Alternatives for Autoimmune Disease Treatments: Physicochemical and Clinical Comparability of Biosimilar Etanercept
title New Alternatives for Autoimmune Disease Treatments: Physicochemical and Clinical Comparability of Biosimilar Etanercept
title_full New Alternatives for Autoimmune Disease Treatments: Physicochemical and Clinical Comparability of Biosimilar Etanercept
title_fullStr New Alternatives for Autoimmune Disease Treatments: Physicochemical and Clinical Comparability of Biosimilar Etanercept
title_full_unstemmed New Alternatives for Autoimmune Disease Treatments: Physicochemical and Clinical Comparability of Biosimilar Etanercept
title_short New Alternatives for Autoimmune Disease Treatments: Physicochemical and Clinical Comparability of Biosimilar Etanercept
title_sort new alternatives for autoimmune disease treatments: physicochemical and clinical comparability of biosimilar etanercept
topic Clinical Study
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4921158/
https://www.ncbi.nlm.nih.gov/pubmed/27382576
http://dx.doi.org/10.1155/2016/9697080
work_keys_str_mv AT mirandahernandezmarianap newalternativesforautoimmunediseasetreatmentsphysicochemicalandclinicalcomparabilityofbiosimilaretanercept
AT lopezmoralescarlosa newalternativesforautoimmunediseasetreatmentsphysicochemicalandclinicalcomparabilityofbiosimilaretanercept
AT perdomoabundezfranciscoc newalternativesforautoimmunediseasetreatmentsphysicochemicalandclinicalcomparabilityofbiosimilaretanercept
AT salazarfloresrodolfod newalternativesforautoimmunediseasetreatmentsphysicochemicalandclinicalcomparabilityofbiosimilaretanercept
AT ramirezibaneznancyd newalternativesforautoimmunediseasetreatmentsphysicochemicalandclinicalcomparabilityofbiosimilaretanercept
AT pereznestoro newalternativesforautoimmunediseasetreatmentsphysicochemicalandclinicalcomparabilityofbiosimilaretanercept
AT molinaperezaaron newalternativesforautoimmunediseasetreatmentsphysicochemicalandclinicalcomparabilityofbiosimilaretanercept
AT revillabeltrijorge newalternativesforautoimmunediseasetreatmentsphysicochemicalandclinicalcomparabilityofbiosimilaretanercept
AT floresortizluisf newalternativesforautoimmunediseasetreatmentsphysicochemicalandclinicalcomparabilityofbiosimilaretanercept
AT medinariveroemilio newalternativesforautoimmunediseasetreatmentsphysicochemicalandclinicalcomparabilityofbiosimilaretanercept