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Recombinant Antibodies for Infectious Diseases

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Attention for Chapter 6: Monoclonal Antibodies and Antibody Like Fragments Derived from Immunised Phage Display Libraries
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Chapter title
Monoclonal Antibodies and Antibody Like Fragments Derived from Immunised Phage Display Libraries
Chapter number 6
Book title
Recombinant Antibodies for Infectious Diseases
Published in
Advances in experimental medicine and biology, January 2017
DOI 10.1007/978-3-319-72077-7_6
Pubmed ID
Book ISBNs
978-3-31-972076-0, 978-3-31-972077-7
Authors

Ubah, Obinna, Palliyil, Soumya

Abstract

Morbidity and mortality associated with infectious diseases are always on the rise, especially in poorer countries and in the aging population. The inevitable, but unpredictable emergence of new infectious diseases has become a global threat. HIV/AIDS, severe acute respiratory syndrome (SARS), and the more recent H1N1 influenza are only a few of the numerous examples of emerging infectious diseases in the modern era. However despite advances in diagnostics, therapeutics and vaccines, there is need for more specific, efficacious, cost-effective and less toxic treatment and preventive drugs. In this chapter, we discuss a powerful combinatorial technology in association with animal immunisation that is capable of generating biologic drugs with high affinity, efficacy and limited off-site toxicity, and diagnostic tools with great precision. Although time consuming, immunisation still remains the preferred route for the isolation of high-affinity antibodies and antibody-like fragments. Phage display is a molecular diversity technology that allows the presentation of large peptide and protein libraries on the surface of filamentous phage. The selection of binding fragments from phage display libraries has proven significant for routine isolation of invaluable peptides, antibodies, and antibody-like domains for diagnostic and therapeutic applications. Here we highlight the many benefits of combining immunisation with phage display in combating infectious diseases, and how our knowledge of antibody engineering has played a crucial role in fully exploiting these platforms in generating therapeutic and diagnostic biologics towards antigenic targets of infectious organisms.

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The data shown below were compiled from readership statistics for 35 Mendeley readers of this research output. Click here to see the associated Mendeley record.

Geographical breakdown

Country Count As %
Unknown 35 100%

Demographic breakdown

Readers by professional status Count As %
Student > Bachelor 9 26%
Student > Master 4 11%
Researcher 4 11%
Other 3 9%
Student > Ph. D. Student 3 9%
Other 3 9%
Unknown 9 26%
Readers by discipline Count As %
Biochemistry, Genetics and Molecular Biology 9 26%
Medicine and Dentistry 3 9%
Agricultural and Biological Sciences 2 6%
Veterinary Science and Veterinary Medicine 2 6%
Immunology and Microbiology 2 6%
Other 5 14%
Unknown 12 34%