Chapter 9 – Biobetter Biologics

Technological advances in the discovery and development of biologics have led to significant product and process improvement, affording drugs that are better for the patient. Biobetters are a new class of biopharmaceutical molecules developed by changes in the molecular profile through chemical, molecular, or functional changes. These changes allow the modified biologic to have considerable enhancements that include, but are not limited to, increased half-life, reduced toxicity, reduced immunogenicity, and enhanced pharmacodynamic effects. Development strategies for the optimization and development of biobetters fall into two major categories: (1) formulation approaches, and (2) protein engineering. This review focuses on the most common approaches to modifying biopharmaceuticals such as PEGylation, recombinant fusions, antibody–drug conjugates, affinity maturation, and antibody engineering and will touch only briefly on formulation approaches.

[1]  J. Reichert Antibodies to watch in 2013 , 2013, mAbs.

[2]  C. Reichel Recent developments in doping testing for erythropoietin , 2011, Analytical and bioanalytical chemistry.

[3]  P. Devroey,et al.  A double-blind, non-inferiority RCT comparing corifollitropin alfa and recombinant FSH during the first seven days of ovarian stimulation using a GnRH antagonist protocol , 2009, Human reproduction.

[4]  K. Shitara,et al.  Engineered therapeutic antibodies with improved effector functions , 2009, Cancer science.

[5]  K. Lundstrom,et al.  Review on Medusa®:a polymer-based sustained release technology for protein and peptide drugs , 2007, Expert opinion on drug delivery.

[6]  Herren Wu,et al.  Structural characterization of a human Fc fragment engineered for extended serum half-life. , 2009, Molecular immunology.

[7]  T. Robak,et al.  New Anti-CD20 Monoclonal Antibodies for the Treatment of B-Cell Lymphoid Malignancies , 2011, BioDrugs.

[8]  Herren Wu,et al.  Properties of Human IgG1s Engineered for Enhanced Binding to the Neonatal Fc Receptor (FcRn)* , 2006, Journal of Biological Chemistry.

[9]  Simona Jevševar,et al.  PEGylation of therapeutic proteins , 2010, Biotechnology journal.

[10]  T. Igawa,et al.  Reduced elimination of IgG antibodies by engineering the variable region. , 2010, Protein engineering, design & selection : PEDS.

[11]  P. Carter Potent antibody therapeutics by design , 2006, Nature Reviews Immunology.

[12]  Gary Walsh,et al.  Biopharmaceutical benchmarks 2010 , 2010, Nature Biotechnology.

[13]  Andrew C. Chan,et al.  Therapeutic antibodies for autoimmunity and inflammation , 2010, Nature Reviews Immunology.

[14]  R. Minter,et al.  Harnessing phage and ribosome display for antibody optimisation. , 2006, Trends in biotechnology.

[15]  Christian Bailly,et al.  Strategies and challenges for the next generation of therapeutic antibodies , 2010, Nature Reviews Immunology.

[16]  M. Otagiri,et al.  Pharmaceutical aspects of the recombinant human serum albumin dimer: structural characteristics, biological properties, and medical applications. , 2012, Journal of pharmaceutical sciences.

[17]  R. Terkeltaub Update on gout: new therapeutic strategies and options , 2010, Nature Reviews Rheumatology.

[18]  Y. Byun,et al.  Synthesis, characterization, and pharmacokinetic studies of PEGylated glucagon-like peptide-1. , 2005, Bioconjugate chemistry.

[19]  R. Levy,et al.  Rituximab chimeric anti-CD20 monoclonal antibody therapy for relapsed indolent lymphoma: half of patients respond to a four-dose treatment program. , 1998, Journal of clinical oncology : official journal of the American Society of Clinical Oncology.

[20]  M. V. Oers CD20 antibodies: type II to tango? , 2012 .

[21]  U. M. Rose,et al.  Pharmacologic profiling of corifollitropin alfa, the first developed sustained follicle stimulant. , 2011, European journal of pharmacology.

[22]  Deirdre Murphy Piedmonte,et al.  Formulation of Neulasta (pegfilgrastim). , 2008, Advanced drug delivery reviews.

[23]  Alain Van Dorsselaer,et al.  Biosimilar, biobetter, and next generation antibody characterization by mass spectrometry. , 2012, Analytical chemistry.

[24]  R. Kontermann,et al.  Improved Pharmacokinetics of Recombinant Bispecific Antibody Molecules by Fusion to Human Serum Albumin* , 2007, Journal of Biological Chemistry.

[25]  J. Gerss,et al.  Anti-Escherichia coli asparaginase antibody levels determine the activity of second-line treatment with pegylated E coli asparaginase: a retrospective analysis within the ALL-BFM trials. , 2011, Blood.

[26]  A. Beck Biosimilar, biobetter and next generation therapeutic antibodies , 2011, mAbs.

[27]  J. Gasdaska,et al.  An afucosylated anti-CD20 monoclonal antibody with greater antibody-dependent cellular cytotoxicity and B-cell depletion and lower complement-dependent cytotoxicity than rituximab. , 2012, Molecular immunology.

[28]  P. V. Schouwenburg,et al.  Immunogenicity of anti-TNF biologic therapies for rheumatoid arthritis , 2013, Nature Reviews Rheumatology.

[29]  V. Launay-Vacher An appraisal of subcutaneous trastuzumab: a new formulation meeting clinical needs , 2013, Cancer Chemotherapy and Pharmacology.

[30]  W. Stemmer,et al.  GLP2-2G-XTEN: A Pharmaceutical Protein with Improved Serum Half-Life and Efficacy in a Rat Crohn’s Disease Model , 2012, PloS one.

[31]  K. Natarajan,et al.  Costimulation blockade with belatacept in renal transplantation. , 2005, The New England journal of medicine.

[32]  L. Rostaing,et al.  A Phase III Study of Belatacept‐based Immunosuppression Regimens versus Cyclosporine in Renal Transplant Recipients (BENEFIT Study) , 2010, American journal of transplantation : official journal of the American Society of Transplantation and the American Society of Transplant Surgeons.

[33]  Herren Wu,et al.  Development of motavizumab, an ultra-potent antibody for the prevention of respiratory syncytial virus infection in the upper and lower respiratory tract. , 2007, Journal of molecular biology.

[34]  S. Langermann,et al.  Increasing the Affinity of a Human IgG1 for the Neonatal Fc Receptor: Biological Consequences1 , 2002, The Journal of Immunology.

[35]  Willem P C Stemmer,et al.  A recombinant polypeptide extends the in vivo half-life of peptides and proteins in a tunable manner , 2009, Nature Biotechnology.

[36]  M. Scholle,et al.  Gcg-XTEN: An Improved Glucagon Capable of Preventing Hypoglycemia without Increasing Baseline Blood Glucose , 2010, PloS one.

[37]  J. Hubbell,et al.  Drug development: longer-lived proteins. , 2012, Chemical Society reviews.

[38]  Jennifer A. Getz,et al.  Site-specific targeting of antibody activity in vivo mediated by disease-associated proteases. , 2012, Journal of controlled release : official journal of the Controlled Release Society.

[39]  S. Walsh,et al.  Extended Nasal Residence Time of Lysostaphin and an Anti-Staphylococcal Monoclonal Antibody by Delivery in Semisolid or Polymeric Carriers , 2004, Pharmaceutical Research.

[40]  J. Meier GLP-1 receptor agonists for individualized treatment of type 2 diabetes mellitus , 2012, Nature Reviews Endocrinology.

[41]  Anna M Wu,et al.  Arming antibodies: prospects and challenges for immunoconjugates , 2005, Nature Biotechnology.

[42]  T. Fleming,et al.  Use of chemotherapy plus a monoclonal antibody against HER2 for metastatic breast cancer that overexpresses HER2. , 2001, The New England journal of medicine.

[43]  W. Stemmer,et al.  A Novel Long-Acting Human Growth Hormone Fusion Protein (VRS-317): Enhanced In Vivo Potency and Half-Life , 2012, Journal of pharmaceutical sciences.

[44]  G. A. Lazar,et al.  Enhanced antibody half-life improves in vivo activity , 2010, Nature Biotechnology.

[45]  Dieter Häussinger,et al.  Peginterferon alfa-2a plus ribavirin for chronic hepatitis C virus infection. , 2002, The New England journal of medicine.

[46]  B. Scallon,et al.  Construction and initial characterization of a mouse-human chimeric anti-TNF antibody. , 1993, Molecular immunology.

[47]  J. Campbell,et al.  Developing the next generation of monoclonal antibodies for the treatment of rheumatoid arthritis , 2011, British journal of pharmacology.

[48]  R. Fischer,et al.  With or Without Sugar? (A)glycosylation of Therapeutic Antibodies , 2013, Molecular Biotechnology.

[49]  G. Losonsky,et al.  Motavizumab for Prophylaxis of Respiratory Syncytial Virus in High-Risk Children: A Noninferiority Trial , 2010, Pediatrics.

[50]  I. Macdougall,et al.  Pharmacology of darbepoetin alfa. , 2007, Nephrology, dialysis, transplantation : official publication of the European Dialysis and Transplant Association - European Renal Association.

[51]  M. P. Griffin,et al.  A Novel Investigational Fc-Modified Humanized Monoclonal Antibody, Motavizumab-YTE, Has an Extended Half-Life in Healthy Adults , 2013, Antimicrobial Agents and Chemotherapy.

[52]  A. Reznick,et al.  Engineering a Potential Antagonist of Human Thyrotropin and Thyroid-stimulating Antibody* , 2001, The Journal of Biological Chemistry.

[53]  P. Carter,et al.  Introduction to current and future protein therapeutics: a protein engineering perspective. , 2011, Experimental cell research.

[54]  Armin Ruf,et al.  Unique carbohydrate–carbohydrate interactions are required for high affinity binding between FcγRIII and antibodies lacking core fucose , 2011, Proceedings of the National Academy of Sciences.

[55]  G. Pietersz,et al.  Fc receptor-targeted therapies for the treatment of inflammation, cancer and beyond , 2012, Nature Reviews Drug Discovery.

[56]  J. Bye,et al.  Isolation of high-affinity monomeric human anti-c-erbB-2 single chain Fv using affinity-driven selection. , 1996, Journal of molecular biology.

[57]  J. Baselga,et al.  Phase I pharmacokinetic and pharmacodynamic dose-escalation study of RG7160 (GA201), the first glycoengineered monoclonal antibody against the epidermal growth factor receptor, in patients with advanced solid tumors. , 2011, Journal of clinical oncology : official journal of the American Society of Clinical Oncology.

[58]  D. Guyer,et al.  Pegaptanib, a targeted anti-VEGF aptamer for ocular vascular disease , 2006, Nature Reviews Drug Discovery.

[59]  S. Kadono,et al.  Novel asymmetrically engineered antibody Fc variant with superior FcγR binding affinity and specificity compared with afucosylated Fc variant , 2013, mAbs.

[60]  M. Crispin,et al.  Engineering Hydrophobic Protein–Carbohydrate Interactions to Fine-Tune Monoclonal Antibodies , 2013, Journal of the American Chemical Society.

[61]  B. Bax,et al.  In vitro and in vivo studies with human carrier erythrocytes loaded with polyethylene glycol‐conjugated and native adenosine deaminase , 2000, British journal of haematology.

[62]  Mariana Henriques,et al.  Guidelines to cell engineering for monoclonal antibody production. , 2010, European journal of pharmaceutics and biopharmaceutics : official journal of Arbeitsgemeinschaft fur Pharmazeutische Verfahrenstechnik e.V.

[63]  M. Bardor,et al.  Minimizing immunogenicity of biopharmaceuticals by controlling critical quality attributes of proteins , 2012, Biotechnology journal.

[64]  P. Linsley,et al.  Rational Development of LEA29Y (belatacept), a High‐Affinity Variant of CTLA4‐Ig with Potent Immunosuppressive Properties , 2005, American journal of transplantation : official journal of the American Society of Transplantation and the American Society of Transplant Surgeons.

[65]  Kenneth Koury,et al.  For Personal Use. Only Reproduce with Permission from the Lancet Publishing Group , 2022 .

[66]  A. Nesbitt,et al.  Mechanism of action of certolizumab pegol (CDP870): In vitro comparison with other anti‐tumor necrosis factor &agr; agents , 2007, Inflammatory bowel diseases.

[67]  C. Ries,et al.  GA201 (RG7160): A Novel, Humanized, Glycoengineered Anti-EGFR Antibody with Enhanced ADCC and Superior In Vivo Efficacy Compared with Cetuximab , 2012, Clinical Cancer Research.

[68]  Thomayant Prueksaritanont,et al.  The impact of sialic acids on the pharmacokinetics of a PEGylated erythropoietin. , 2012, Journal of pharmaceutical sciences.

[69]  Teresa Mitchell,et al.  Optimization of erythropoietin production with controlled glycosylation-PEGylated erythropoietin produced in glycoengineered Pichia pastoris. , 2012, Journal of biotechnology.

[70]  Rachel M. Devay,et al.  Increasing Serum Half-life and Extending Cholesterol Lowering in Vivo by Engineering Antibody with pH-sensitive Binding to PCSK9* , 2012, The Journal of Biological Chemistry.

[71]  J. A. Scarlett,et al.  Long-term treatment of acromegaly with pegvisomant, a growth hormone receptor antagonist , 2001, The Lancet.

[72]  Youwei Jiang,et al.  Optimization of humanized IgGs in glycoengineered Pichia pastoris , 2006, Nature Biotechnology.

[73]  R. Pettengell,et al.  Use of Filgrastim and Pegfilgrastim to Support Delivery of Chemotherapy , 2012, BioDrugs.

[74]  Bruce Tidor,et al.  Aglycosylated immunoglobulin G1 variants productively engage activating Fc receptors , 2008, Proceedings of the National Academy of Sciences.

[75]  M. Sliwkowski,et al.  Superior in vivo efficacy of afucosylated trastuzumab in the treatment of HER2-amplified breast cancer. , 2010, Cancer research.

[76]  V. Tesar,et al.  Discovery and basic pharmacology of erythropoiesis-stimulating agents (ESAs), including the hyperglycosylated ESA, darbepoetin alfa: an update of the rationale and clinical impact , 2010, European Journal of Clinical Pharmacology.

[77]  W. Jusko,et al.  Pharmacokinetics and Antibody Responses to the CD3 Antibody Otelixizumab Used in the Treatment of Type 1 Diabetes , 2010, Journal of clinical pharmacology.

[78]  Bethan Hughes Gearing up for follow-on biologics , 2009, Nature reviews. Drug discovery.

[79]  Thomas H Pillow,et al.  Antibody‐Drug Conjugates for the Treatment of Cancer , 2013, Chemical biology & drug design.

[80]  Jill Crouse-Zeineddini,et al.  Biochemical assessment of erythropoietin products from Asia versus US Epoetin alfa manufactured by Amgen. , 2009, Journal of pharmaceutical sciences.

[81]  Jiandu Lei,et al.  Enhanced circulation half-life of site-specific PEGylated rhG-CSF: optimization of PEG molecular weight. , 2009, Journal of biotechnology.