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Assessment of immunogenicity of romiplostim in clinical studies with ITP subjects

Romiplostim is an Fc-peptide fusion protein that activates intracellular transcriptional pathways via the thrombopoietin (TPO) receptor leading to increased platelet production. Romiplostim has been engineered to have no amino acid sequence homology to endogenous TPO. Recombinant protein therapeutic...

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Autores principales: Jawa, Vibha, Hokom, Martha, Hu, Zheng, El-Abaadi, Naglaa, Zhuang, Yao, Berger, Dietmar, Gupta, Shalini, Swanson, Steven J., Chirmule, Narendra
Formato: Texto
Lenguaje:English
Publicado: Springer-Verlag 2010
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2900600/
https://www.ncbi.nlm.nih.gov/pubmed/20155267
http://dx.doi.org/10.1007/s00277-010-0908-2
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author Jawa, Vibha
Hokom, Martha
Hu, Zheng
El-Abaadi, Naglaa
Zhuang, Yao
Berger, Dietmar
Gupta, Shalini
Swanson, Steven J.
Chirmule, Narendra
author_facet Jawa, Vibha
Hokom, Martha
Hu, Zheng
El-Abaadi, Naglaa
Zhuang, Yao
Berger, Dietmar
Gupta, Shalini
Swanson, Steven J.
Chirmule, Narendra
author_sort Jawa, Vibha
collection PubMed
description Romiplostim is an Fc-peptide fusion protein that activates intracellular transcriptional pathways via the thrombopoietin (TPO) receptor leading to increased platelet production. Romiplostim has been engineered to have no amino acid sequence homology to endogenous TPO. Recombinant protein therapeutics can be at a risk of development of an antibody response that can impact efficacy and safety. Hence, a strategy to detect potential antibody formation to the drug and to related endogenous molecules can be useful. The immunogenicity assessment strategy involved both the detection and characterization of binding and neutralizing antibodies. The method for detection was based on a surface plasmon resonance biosensor platform using the Biacore 3000. Samples that tested positive for binding antibodies in the Biacore immunoassay were then tested in a neutralization assay. Serum samples from 225 subjects with immune thrombocytopenic purpura (ITP) dosed with romiplostim and 45 ITP subjects dosed with placebo were tested for romiplostim and TPO antibodies. Prior to romiplostim treatment, 17 subjects (7%) tested romiplostim antibody positive and 12 subjects (5%) tested TPO antibody positive for pre-existing binding antibodies. After romiplostim exposure, 11% of the subjects exhibited binding antibodies against romiplostim and 5% of the subjects with ITP showed binding antibodies against TPO. The antibodies against romiplostim did not cross-react with TPO and vice versa. No cases of anti-TPO neutralizing antibodies were detected in romiplostim-treated subjects. The incidence of anti-romiplostim neutralizing antibodies to romiplostim was 0.4% (one subject); this subject tested negative at the time of follow-up 4 months later. No impact on platelet profiles were apparent in subjects that had antibodies to romiplostim to date. In summary, administration of romiplostim in ITP subjects resulted in the development of a binding antibody response against romiplostim and TPO ligand. One subject developed a neutralizing antibody response to romiplostim that impacted the platelet counts of this subject. No neutralizing antibodies to endogenous TPO were observed.
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spelling pubmed-29006002010-07-30 Assessment of immunogenicity of romiplostim in clinical studies with ITP subjects Jawa, Vibha Hokom, Martha Hu, Zheng El-Abaadi, Naglaa Zhuang, Yao Berger, Dietmar Gupta, Shalini Swanson, Steven J. Chirmule, Narendra Ann Hematol Original Article Romiplostim is an Fc-peptide fusion protein that activates intracellular transcriptional pathways via the thrombopoietin (TPO) receptor leading to increased platelet production. Romiplostim has been engineered to have no amino acid sequence homology to endogenous TPO. Recombinant protein therapeutics can be at a risk of development of an antibody response that can impact efficacy and safety. Hence, a strategy to detect potential antibody formation to the drug and to related endogenous molecules can be useful. The immunogenicity assessment strategy involved both the detection and characterization of binding and neutralizing antibodies. The method for detection was based on a surface plasmon resonance biosensor platform using the Biacore 3000. Samples that tested positive for binding antibodies in the Biacore immunoassay were then tested in a neutralization assay. Serum samples from 225 subjects with immune thrombocytopenic purpura (ITP) dosed with romiplostim and 45 ITP subjects dosed with placebo were tested for romiplostim and TPO antibodies. Prior to romiplostim treatment, 17 subjects (7%) tested romiplostim antibody positive and 12 subjects (5%) tested TPO antibody positive for pre-existing binding antibodies. After romiplostim exposure, 11% of the subjects exhibited binding antibodies against romiplostim and 5% of the subjects with ITP showed binding antibodies against TPO. The antibodies against romiplostim did not cross-react with TPO and vice versa. No cases of anti-TPO neutralizing antibodies were detected in romiplostim-treated subjects. The incidence of anti-romiplostim neutralizing antibodies to romiplostim was 0.4% (one subject); this subject tested negative at the time of follow-up 4 months later. No impact on platelet profiles were apparent in subjects that had antibodies to romiplostim to date. In summary, administration of romiplostim in ITP subjects resulted in the development of a binding antibody response against romiplostim and TPO ligand. One subject developed a neutralizing antibody response to romiplostim that impacted the platelet counts of this subject. No neutralizing antibodies to endogenous TPO were observed. Springer-Verlag 2010-02-13 2010 /pmc/articles/PMC2900600/ /pubmed/20155267 http://dx.doi.org/10.1007/s00277-010-0908-2 Text en © The Author(s) 2010 https://creativecommons.org/licenses/by-nc/4.0/ This article is distributed under the terms of the Creative Commons Attribution Noncommercial License which permits any noncommercial use, distribution, and reproduction in any medium, provided the original author(s) and source are credited.
spellingShingle Original Article
Jawa, Vibha
Hokom, Martha
Hu, Zheng
El-Abaadi, Naglaa
Zhuang, Yao
Berger, Dietmar
Gupta, Shalini
Swanson, Steven J.
Chirmule, Narendra
Assessment of immunogenicity of romiplostim in clinical studies with ITP subjects
title Assessment of immunogenicity of romiplostim in clinical studies with ITP subjects
title_full Assessment of immunogenicity of romiplostim in clinical studies with ITP subjects
title_fullStr Assessment of immunogenicity of romiplostim in clinical studies with ITP subjects
title_full_unstemmed Assessment of immunogenicity of romiplostim in clinical studies with ITP subjects
title_short Assessment of immunogenicity of romiplostim in clinical studies with ITP subjects
title_sort assessment of immunogenicity of romiplostim in clinical studies with itp subjects
topic Original Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2900600/
https://www.ncbi.nlm.nih.gov/pubmed/20155267
http://dx.doi.org/10.1007/s00277-010-0908-2
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