Abstract

Therapeutic protein drugs are an important class of medicines serving patients most in need of novel therapies. Recently approved recombinant protein therapeutics have been developed to treat a wide variety of clinical indications, including cancers, autoimmunity/inflammation, exposure to infectious agents, and genetic disorders. The latest advances in protein-engineering technologies have allowed drug developers and manufacturers to fine-tune and exploit desirable functional characteristics of proteins of interest while maintaining (and in some cases enhancing) product safety or efficacy or both. In this review, we highlight the emerging trends and approaches in protein drug development by using examples of therapeutic proteins approved by the U.S. Food and Drug Administration over the previous five years (2011–2016, namely January 1, 2011, through August 31, 2016).

Highlights

  • Therapeutic protein drugs are an important class of medicines serving patients most in need of novel therapies

  • Protein therapeutics cannot be completely synthesized by chemical processes and have to be manufactured in living cells or organisms; the choices of the cell line, species origin, and culture conditions all affect the final product characteristics[5,6,7]

  • Given the complexity of therapeutic proteins with respect to their large molecular size, post-translational modifications, and the variety of biological materials involved in their manufacturing process, the ability to enhance particular functional attributes while maintaining product safety and efficacy achieved through protein-engineering strategies is highly desirable

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Summary

Schellekens H

Biosimilar therapeutics-what do we need to consider? NDT Plus. 2009; 2(Suppl_1): i27–i36. Biosimilar therapeutics-what do we need to consider? 5. Bandaranayake AD, Almo SC: Recent advances in mammalian protein production. 6. Butler M, Meneses-Acosta A: Recent advances in technology supporting biopharmaceutical production from mammalian cells. 7. Zhu J: Mammalian cell protein expression for biopharmaceutical production. Cipriano D, Burnham M, Hughes JV: Effectiveness of various processing steps for viral clearance of therapeutic proteins: database analyses of commonly used steps. 9. Chirino AJ, Mire-Sluis A: Characterizing biological products and assessing comparability following manufacturing changes.

12. Lutz S
17. Strohl WR
20. Jefferis R
38. Food and Drug Administration
46. Houdebine LM
50. Fox JL
61. Food and Drug Administration
68. Pescovitz MD
PubMed Abstract
Findings
72. Beck A
Full Text
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