Literature DB >> 17337334

Immunogenicity of therapeutic proteins. Part 3: impact of manufacturing changes.

Basant Sharma1.   

Abstract

Immunogenicity of biopharmaceuticals relates to the intrinsic complexity of proteins as well as the complexities of the manufacturing process. The manufacture of biopharmaceuticals involves a number of complex processing steps designed to create a highly pure, stable, safe, and effective product. The process often lasts many months and can be divided into seven stages - host cell development, master cell bank establishment, protein production, purification, analysis, formulation, and storage and handling. Even minor variations at any of these stages can lead to clinically relevant changes in efficacy and/or safety of the end product. Due to the complexity of the process and the inherently unstable nature of proteins outside the body, compositional changes can occur, leading to decreased biological activity, alteration of molecular structure, and possible increased risk of host immune responses following administration. Examples are discussed whereby immunogenicity associated with some of these changes has occurred with potentially serious clinical consequences.

Mesh:

Substances:

Year:  2007        PMID: 17337334     DOI: 10.1016/j.biotechadv.2007.01.007

Source DB:  PubMed          Journal:  Biotechnol Adv        ISSN: 0734-9750            Impact factor:   14.227


  19 in total

Review 1.  Fabry disease, enzyme replacement therapy and the significance of antibody responses.

Authors:  Patrick B Deegan
Journal:  J Inherit Metab Dis       Date:  2011-10-25       Impact factor: 4.982

2.  Traceability of biopharmaceuticals in spontaneous reporting systems: a cross-sectional study in the FDA Adverse Event Reporting System (FAERS) and EudraVigilance databases.

Authors:  Niels S Vermeer; Sabine M J M Straus; Aukje K Mantel-Teeuwisse; Francois Domergue; Toine C G Egberts; Hubert G M Leufkens; Marie L De Bruin
Journal:  Drug Saf       Date:  2013-08       Impact factor: 5.606

3.  Biosimilars 2.0: guiding principles for a global "patients first" standard.

Authors:  Joseph Miletich; Geoffrey Eich; Gustavo Grampp; Barbara Mounho
Journal:  MAbs       Date:  2011-05-01       Impact factor: 5.857

Review 4.  Biosimilar: what it is not.

Authors:  Fernando de Mora
Journal:  Br J Clin Pharmacol       Date:  2015-06-04       Impact factor: 4.335

Review 5.  Safety of Biologics, Including Biosimilars: Perspectives on Current Status and Future Direction.

Authors:  Ylenia Ingrasciotta; Paola M Cutroneo; Ilaria Marcianò; Thijs Giezen; Fabiola Atzeni; Gianluca Trifirò
Journal:  Drug Saf       Date:  2018-11       Impact factor: 5.606

6.  Risk-Based Comparability Assessment for Monoclonal Antibodies During Drug Development: A Clinical Pharmacology Perspective.

Authors:  Yanli Zhuang; Di Chen; Amarnath Sharma; Zhenhua Xu
Journal:  AAPS J       Date:  2018-10-15       Impact factor: 4.009

7.  Evaluating Immunogenicity Risk Due to Host Cell Protein Impurities in Antibody-Based Biotherapeutics.

Authors:  Vibha Jawa; Marisa K Joubert; Qingchun Zhang; Meghana Deshpande; Suminda Hapuarachchi; Michael P Hall; Gregory C Flynn
Journal:  AAPS J       Date:  2016-07-22       Impact factor: 4.009

8.  Tungsten-induced denaturation and aggregation of epoetin alfa during primary packaging as a cause of immunogenicity.

Authors:  Andreas Seidl; Otmar Hainzl; Marleen Richter; Robert Fischer; Stephan Böhm; Britta Deutel; Martin Hartinger; Jörg Windisch; Nicole Casadevall; Gerard Michel London; Iain Macdougall
Journal:  Pharm Res       Date:  2011-11-18       Impact factor: 4.200

9.  Characterization of Aggregation Propensity of a Human Fc-Fusion Protein Therapeutic by Hydrogen/Deuterium Exchange Mass Spectrometry.

Authors:  Richard Y-C Huang; Roxana E Iacob; Stanley R Krystek; Mi Jin; Hui Wei; Li Tao; Tapan K Das; Adrienne A Tymiak; John R Engen; Guodong Chen
Journal:  J Am Soc Mass Spectrom       Date:  2016-08-15       Impact factor: 3.109

Review 10.  Analytical tools for characterizing biopharmaceuticals and the implications for biosimilars.

Authors:  Steven A Berkowitz; John R Engen; Jeffrey R Mazzeo; Graham B Jones
Journal:  Nat Rev Drug Discov       Date:  2012-06-29       Impact factor: 84.694

View more

北京卡尤迪生物科技股份有限公司 © 2022-2023.