Literature DB >> 19963283

Immunological mechanism underlying the immune response to recombinant human protein therapeutics.

Melody Sauerborn1, Vera Brinks, Wim Jiskoot, Huub Schellekens.   

Abstract

Recombinant human (rhu) protein therapeutics are powerful tools to treat several severe diseases such as multiple sclerosis and diabetes mellitus, among others. A major drawback of these proteins is the production of anti-drug antibodies (ADAs). In some cases, these ADAs have neutralizing capacity and can interfere with the efficacy and safety of the drug. Little is known about the immunological mechanisms underlying the unwanted immune response against human homolog protein therapeutics. This article aims to provide current insights into recent immunological developments and to link this with regard to production of ADAs. A particular focus is given to aggregates being present in a rhu protein formulation and their impact on the immune system, subsequently leading to breakage of tolerance and formation of ADAs. Aggregation is one of the key factors in immunogenicity and by reducing aggregation one can reduce immunogenicity and make drugs safer and more efficient. Copyright 2009 Elsevier Ltd. All rights reserved.

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Year:  2009        PMID: 19963283     DOI: 10.1016/j.tips.2009.11.001

Source DB:  PubMed          Journal:  Trends Pharmacol Sci        ISSN: 0165-6147            Impact factor:   14.819


  56 in total

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4.  Coupling of aggregation and immunogenicity in biotherapeutics: T- and B-cell immune epitopes may contain aggregation-prone regions.

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Journal:  Pharm Res       Date:  2011-03-25       Impact factor: 4.200

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Authors:  Moin Vera; Thomas Lester; Bin Zhao; Pascale Tiger; Scott Clarke; Brigette L Tippin; Merry B Passage; Steven Q Le; Javier Femenia; Jeffrey F Lemontt; Emil D Kakkis; Patricia I Dickson
Journal:  JIMD Rep       Date:  2012-07-06

6.  Computational tools help improve protein stability but with a solubility tradeoff.

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Journal:  J Biol Chem       Date:  2017-07-14       Impact factor: 5.157

Review 7.  Absorption, distribution, metabolism, and excretion (ADME) studies of biotherapeutics for autoimmune and inflammatory conditions.

Authors:  Yulia Vugmeyster; John Harrold; Xin Xu
Journal:  AAPS J       Date:  2012-07-14       Impact factor: 4.009

Review 8.  Preclinical models used for immunogenicity prediction of therapeutic proteins.

Authors:  Vera Brinks; Daniel Weinbuch; Matthew Baker; Yann Dean; Philippe Stas; Stefan Kostense; Bonita Rup; Wim Jiskoot
Journal:  Pharm Res       Date:  2013-05-07       Impact factor: 4.200

Review 9.  Immunogenicity Risk Assessment for an Engineered Human Cytokine Analogue Expressed in Different Cell Substrates.

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Journal:  AAPS J       Date:  2020-04-14       Impact factor: 4.009

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Journal:  JCI Insight       Date:  2016-02-25
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