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Therapeutic use of specific tumour necrosis factor inhibitors in inflammatory diseases including COVID-19

Biomedicine & pharmacotherapy, 2021-08, Vol.140, p.111785-111785, Article 111785

2021

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Maintaining ‘standards’ for biosimilar monoclonal antibodies

Nature biotechnology, 2021-03, Vol.39 (3), p.276-280

2021

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Biosimilars: what clinicians should know

Blood, 2012-12, Vol.120 (26), p.5111-5117

2012

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The First WHO International Standard for Adalimumab: Dual Role in Bioactivity and Therapeutic Drug Monitoring

Frontiers in immunology, 2021-04, Vol.12, p.636420-636420

2021

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"Cytokine Storm" in the Phase I Trial of Monoclonal Antibody TGN1412: Better Understanding the Causes to Improve PreClinical Testing of Immunotherapeutics

Journal of Immunology, 2007-09, Vol.179 (5), p.3325-3331

2007

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The First WHO International Standard for Harmonizing the Biological Activity of Bevacizumab

Biomolecules (Basel, Switzerland), 2021-10, Vol.11 (11), p.1610

2021

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Haematopoietic growth factors and their therapeutic use

Thrombosis and haemostasis, 2008-05, Vol.99 (5), p.863-873

2008

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Impact of Formulation Choices on the Freeze-Drying of an Interleukin-6 Reference Material

Frontiers in molecular biosciences, 2022-07, Vol.9, p.868460-868460

2022

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Surrogate CD16-expressing effector cell lines for determining the bioactivity of therapeutic monoclonal antibodies

Journal of pharmaceutical and biomedical analysis, 2017-09, Vol.143, p.188-198

2017

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Editor's Highlight: Subvisible Aggregates of Immunogenic Proteins Promote a Th1-Type Response

Toxicological sciences, 2016-10, Vol.153 (2), p.258-270

2016

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Detection of neutralizing antibodies to erythropoietin by inhibition of rHuEPO-stimulated EGR1 gene expression in the UT-7/EPO cell line

Journal of immunological methods, 2013-01, Vol.387 (1-2), p.191-198

2013

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Harmonization and standardization of immunogenicity assessment of biotherapeutic products

Bioanalysis, 2019-09, Vol.11 (17), p.1593-1604

2019

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Bioanalytical strategies in determining immunogenicity

Bioanalysis, 2019-09, Vol.11 (17), p.1535-1537

2019

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WHO International Standards and reference preparations for cytokines and growth factors

Cytokine (Philadelphia, Pa.), 2019-11, Vol.123, p.154797-154797, Article 154797

2019

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Unwanted Immunogenicity: Implications for Follow-on Biologicals

Drug information journal, 2007-01, Vol.41 (1), p.1-9

2007

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The importance of World Health Organization international reference standards in the product life cycle of biosimilars

Annals of the New York Academy of Sciences, 2024-10, Vol.1540 (1), p.225-234

2024

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Immunogenicity assessment of biotherapeutic products: An overview of assays and their utility

Biologicals, 2015-09, Vol.43 (5), p.298-306

2015

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WHO guidelines on biosimilars: Toward improved access to safe and effective products

Annals of the New York Academy of Sciences, 2023-03, Vol.1521 (1), p.96-103

2023

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Endothelial cell functions impaired by interferon in vitro: Insights into the molecular mechanism of thrombotic microangiopathy associated with interferon therapy

Thrombosis research, 2018-03, Vol.163, p.105-116

2018

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Detection of anti-cytokine antibodies and their clinical relevance

Expert review of clinical immunology, 2014-08, Vol.10 (8), p.1029-1047

2014

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IL-27 Promotes Proliferation of Human Leukemic Cell Lines Through the MAPK/ERK Signaling Pathway and Suppresses Sensitivity to Chemotherapeutic Drugs

Journal of interferon & cytokine research, 2016-05, Vol.36 (5), p.302-316

2016

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Anti-therapeutic antibodies and their clinical impact in patients treated with the TNF antagonist adalimumab

Cytokine (Philadelphia, Pa.), 2017-08, Vol.96, p.16-23

2017

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WHO International Standards and Reference Preparations for Cytokines and Growth Factors

Journal of leukocyte biology, 2020-01, Vol.107 (1), p.159-160

2020

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Biosimilars—why terminology matters

Nature biotechnology, 2011-08, Vol.29 (8), p.690-693

2011

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Unwanted immunogenicity: lessons learned and future challenges

Bioanalysis, 2010-06, Vol.2 (6), p.1073-1084

2010

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Therapeutic use of specific tumour necrosis factor inhibitors in inflammatory diseases including COVID-19

Maintaining ‘standards’ for biosimilar monoclonal antibodies

Biosimilars: what clinicians should know

The First WHO International Standard for Adalimumab: Dual Role in Bioactivity and Therapeutic Drug Monitoring

"Cytokine Storm" in the Phase I Trial of Monoclonal Antibody TGN1412: Better Understanding the Causes to Improve PreClinical Testing of Immunotherapeutics

The First WHO International Standard for Harmonizing the Biological Activity of Bevacizumab

Haematopoietic growth factors and their therapeutic use

Impact of Formulation Choices on the Freeze-Drying of an Interleukin-6 Reference Material

Surrogate CD16-expressing effector cell lines for determining the bioactivity of therapeutic monoclonal antibodies

Editor's Highlight: Subvisible Aggregates of Immunogenic Proteins Promote a Th1-Type Response

Detection of neutralizing antibodies to erythropoietin by inhibition of rHuEPO-stimulated EGR1 gene expression in the UT-7/EPO cell line

Harmonization and standardization of immunogenicity assessment of biotherapeutic products

Bioanalytical strategies in determining immunogenicity

WHO International Standards and reference preparations for cytokines and growth factors

Unwanted Immunogenicity: Implications for Follow-on Biologicals

The importance of World Health Organization international reference standards in the product life cycle of biosimilars

Immunogenicity assessment of biotherapeutic products: An overview of assays and their utility

WHO guidelines on biosimilars: Toward improved access to safe and effective products

Endothelial cell functions impaired by interferon in vitro: Insights into the molecular mechanism of thrombotic microangiopathy associated with interferon therapy

Detection of anti-cytokine antibodies and their clinical relevance

IL-27 Promotes Proliferation of Human Leukemic Cell Lines Through the MAPK/ERK Signaling Pathway and Suppresses Sensitivity to Chemotherapeutic Drugs

Anti-therapeutic antibodies and their clinical impact in patients treated with the TNF antagonist adalimumab

WHO International Standards and Reference Preparations for Cytokines and Growth Factors

Biosimilars—why terminology matters

Unwanted immunogenicity: lessons learned and future challenges

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