Literature DB >> 25090369

Shark variable new antigen receptor biologics - a novel technology platform for therapeutic drug development.

Marina Kovaleva1, Laura Ferguson, John Steven, Andrew Porter, Caroline Barelle.   

Abstract

INTRODUCTION: Biologics drugs have succeeded in achieving a commercial dominance in the global market for new therapies and large pharmaceutical companies' interest remains strong through a continued commitment to pipeline development. It is not surprising, therefore, that next-generation biologics, particularly antibody-like scaffolds that offer many of the advantages of the original biologic drugs but in simplified formats, have entered the clinic as competing substitute therapeutic products, to capture market share. AREAS COVERED: Specifically, this paper will position shark-derived variable new antigen receptors (VNARs) within an overview of the existing biologics landscape including the growth, diversity and success to date of alternative scaffolds. The intention is not to provide a comprehensive review of biologics as a whole but to discuss the main competing single-domain technologies and the exciting therapeutic potential of VNAR domains as clinical candidates within this context. EXPERT OPINION: The inherent ability to specifically bind target and intervene in disease-related biological processes, while reducing off-site toxicity, makes mAbs an effective, potent and now proven class of therapeutics. There are, however, limitations to these 'magic bullets'. Their size and complexity can restrict their utility in certain diseases types and disease locations. In contrast, a number of so-called alternative scaffolds, derived from both immunoglobulin- and non-immunoglobulin-based sources have been developed with real potential to overcome many of the shortcomings documented for mAb treatments. Unlike competing approaches such as Darpins and Affibodies, we now know that shark VNAR domains (like camel VHH nanobody domains), are an integral part of the adaptive immune system of these animals and have evolved naturally (but from very different starting molecules) to exhibit high affinity and selectivity for target. In addition, and again influenced by the environment in which they have evolved naturally, their small size, simple architecture, high solubility and stability, deliver additional flexibility compared to classical antibodies (and many non-natural alternative scaffolds), thereby providing an attractive basis for particular clinical indications where these attributes may offer advantages.

Entities:  

Keywords:  binding domains; biologics; drug development; mAb; novel scaffolds; shark; variable new antigen receptor

Mesh:

Substances:

Year:  2014        PMID: 25090369     DOI: 10.1517/14712598.2014.937701

Source DB:  PubMed          Journal:  Expert Opin Biol Ther        ISSN: 1471-2598            Impact factor:   4.388


  31 in total

1.  Molecular Origin of the Stability Difference in Four Shark IgNAR Constant Domains.

Authors:  Hong Zhou; Shengtang Liu; Xiuhua Yin; Zengpeng Li; Zaixing Yang; Ruhong Zhou
Journal:  Biophys J       Date:  2019-04-22       Impact factor: 4.033

Review 2.  Structural and genetic diversity in antibody repertoires from diverse species.

Authors:  Miguel de los Rios; Michael F Criscitiello; Vaughn V Smider
Journal:  Curr Opin Struct Biol       Date:  2015-07-17       Impact factor: 6.809

Review 3.  Peptide aptamers: development and applications.

Authors:  Sergey Reverdatto; David S Burz; Alexander Shekhtman
Journal:  Curr Top Med Chem       Date:  2015       Impact factor: 3.295

4.  Overview, Generation, and Significance of Variable New Antigen Receptors (VNARs) as a Platform for Drug and Diagnostic Development.

Authors:  Samata S Pandey; Marina Kovaleva; Caroline J Barelle; Obinna C Ubah
Journal:  Methods Mol Biol       Date:  2022

5.  Structural insights and biomedical potential of IgNAR scaffolds from sharks.

Authors:  Stefan Zielonka; Martin Empting; Julius Grzeschik; Doreen Könning; Caroline J Barelle; Harald Kolmar
Journal:  MAbs       Date:  2015       Impact factor: 5.857

Review 6.  An update on antibody-based immunotherapies for Clostridium difficile infection.

Authors:  Greg Hussack; Jamshid Tanha
Journal:  Clin Exp Gastroenterol       Date:  2016-08-01

Review 7.  Fish Immunoglobulins.

Authors:  Sara Mashoof; Michael F Criscitiello
Journal:  Biology (Basel)       Date:  2016-11-21

Review 8.  Shark New Antigen Receptor (IgNAR): Structure, Characteristics and Potential Biomedical Applications.

Authors:  Salma Nassor Juma; Xiaoxia Gong; Sujie Hu; Zhengbing Lv; Jianzhong Shao; Lili Liu; Guiqian Chen
Journal:  Cells       Date:  2021-05-08       Impact factor: 6.600

9.  Importance of Hypervariable Region 2 for Stability and Affinity of a Shark Single-Domain Antibody Specific for Ebola Virus Nucleoprotein.

Authors:  George P Anderson; Daniel D Teichler; Dan Zabetakis; Lisa C Shriver-Lake; Jinny L Liu; Stephen G Lonsdale; Sarah A Goodchild; Ellen R Goldman
Journal:  PLoS One       Date:  2016-08-05       Impact factor: 3.240

10.  Semi-synthetic vNAR libraries screened against therapeutic antibodies primarily deliver anti-idiotypic binders.

Authors:  Doreen Könning; Laura Rhiel; Martin Empting; Julius Grzeschik; Carolin Sellmann; Christian Schröter; Stefan Zielonka; Stephan Dickgießer; Thomas Pirzer; Desislava Yanakieva; Stefan Becker; Harald Kolmar
Journal:  Sci Rep       Date:  2017-08-29       Impact factor: 4.379

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