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Vaccine Design

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Cover of 'Vaccine Design'

Table of Contents

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    Book Overview
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    Chapter 1 Challenges in Veterinary Vaccine Development and Immunization.
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    Chapter 2 Development of Mycoplasma hyopneumoniae Recombinant Vaccines.
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    Chapter 3 Computational Prediction of Immunodominant Epitopes on Outer Membrane Protein (Omp) H of Pasteurella multocida Toward Designing of a Peptide Vaccine.
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    Chapter 4 DNA Vaccines Against Maedi-Visna Virus.
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    Chapter 5 Detection of Avian Antigen-Specific T Cells Induced by Viral Vaccines.
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    Chapter 6 Generation of Newcastle Disease Virus (NDV) Recombinants Expressing the Infectious Laryngotracheitis Virus (ILTV) Glycoprotein gB or gD as Dual Vaccines.
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    Chapter 7 Vaccine Design
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    Chapter 8 Development of Fasciola Vaccine in an Animal Model.
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    Chapter 9 Development of Experimental Vaccines Against Liver Flukes.
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    Chapter 10 Vaccine Design
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    Chapter 11 DNA Vaccination in Chickens.
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    Chapter 12 Selection of Vaccine Candidates for Fish Pasteurellosis Using Reverse Vaccinology and an In Vitro Screening Approach.
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    Chapter 13 Development of Vaccines Against Nocardiosis in Fishes.
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    Chapter 14 Design of an Immersion Vaccine Against Aeromonad Septicemia in Perch (Perca fluviatilis L.).
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    Chapter 15 Prokaryotic Production of Virus-Like Particle Vaccine of Betanodavirus.
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    Chapter 16 Design and Construction of Shrimp Antiviral DNA Vaccines Expressing Long and Short Hairpins for Protection by RNA Interference.
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    Chapter 17 Developing Anti-tick Vaccines.
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    Chapter 18 Host Immunization with Recombinant Proteins to Screen Antigens for Tick Control.
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    Chapter 19 Vaccinomics Approach to Tick Vaccine Development.
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    Chapter 20 Vaccine Design
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    Chapter 21 Vaccine Design
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    Chapter 22 Alphavirus-Based Vaccines.
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    Chapter 23 Vaccine Design: Replication-Defective Adenovirus Vectors.
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    Chapter 24 Generation of Lymphocytic Choriomeningitis Virus Based Vaccine Vectors.
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    Chapter 25 Production of Japanese Encephalitis Virus-Like Particles Using Insect Cell Expression Systems.
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    Chapter 26 Subunit Protein Vaccine Delivery System for Tuberculosis Based on Hepatitis B Virus Core VLP (HBc-VLP) Particles.
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    Chapter 27 Formulation Studies During Preclinical Development of Influenza Hemagglutinin and Virus-Like Particle Vaccine Candidates.
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    Chapter 28 Strategies for Vaccine Design Using Phage Display-Derived Peptides.
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    Chapter 29 Production of Well-Characterized Virus-like Particles in an Escherichia coli-Based Expression Platform for Preclinical Vaccine Assessments.
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    Chapter 30 Vaccine Design
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    Chapter 31 Vaccine Design
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    Chapter 32 Vaccine Design
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    Chapter 33 Facile Method for the Production of Recombinant Cholera Toxin B Subunit in E. coli.
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    Chapter 34 Immunoproteomic Approach for Screening Vaccine Candidates from Bacterial Outer Membrane Proteins.
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    Chapter 35 Vaccine Design
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    Chapter 36 Oral Rabies Vaccine Design for Expression in Plants.
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    Chapter 37 Purification of Virus-Like Particles (VLPs) from Plants.
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    Chapter 38 Transient Expression of Viral Proteins in Plants Using Agrobacterium tumefaciens.
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    Chapter 39 Vaccine Design
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    Chapter 40 Recombinant Botulinum Toxoids: A Practical Guide for Production.
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    Chapter 41 Preparation of Multifunctional Liposomes as a Stable Vaccine Delivery-Adjuvant System by Procedure of Emulsification-Lyophilization.
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    Chapter 42 Preparation of the Multifunctional Liposome-Containing Microneedle Arrays as an Oral Cavity Mucosal Vaccine Adjuvant-Delivery System.
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    Chapter 43 Preparation and Characterization of PLGA Encapsulated Protective Antigen Domain 4 Nanoformulation.
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    Chapter 44 Attenuated Salmonella sp. as a DNA Delivery System for Trypanosoma cruzi Antigens.
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    Chapter 45 Poly-ε-caprolactone/Chitosan and Chitosan Particles: Two Recombinant Antigen Delivery Systems for Intranasal Vaccination.
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    Chapter 46 Micro-fractional Epidermal Powder Delivery for Skin Vaccination.
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    Chapter 47 Vaccine Design
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    Chapter 48 The Web-Based DNA Vaccine Database DNAVaxDB and Its Usage for Rational DNA Vaccine Design.
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    Chapter 49 MetaMHCpan, A Meta Approach for Pan-Specific MHC Peptide Binding Prediction.
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    Chapter 50 A Cohesive and Integrated Platform for Immunogenicity Prediction.
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    Chapter 51 The Regulatory Evaluation of Vaccines for Human Use.
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    Chapter 52 Vaccines and IP Rights: A Multifaceted Relationship.
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    Chapter 53 From the Bench to the Pharmacy: Protecting Innovation During Vaccine Development and Commercialization.
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    Chapter 54 Intellectual Property in Vaccine Innovation: Impact of Recent Patent Developments.
Attention for Chapter 36: Oral Rabies Vaccine Design for Expression in Plants.
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Chapter title
Oral Rabies Vaccine Design for Expression in Plants.
Chapter number 36
Book title
Vaccine Design
Published in
Methods in molecular biology, January 2016
DOI 10.1007/978-1-4939-3389-1_36
Pubmed ID
Book ISBNs
978-1-4939-3388-4, 978-1-4939-3389-1
Authors

Ankit Singh, Gauri Saxena, Praveen C. Verma

Editors

Sunil Thomas

Abstract

Vaccination is the sensitization process of the immune system against any pathogen. Generally, recombinant subunit vaccines are considered safer than attenuated vaccines. As whole pathogenic organisms are used in the immunization process, the attenuated vaccines are considered more risky than subunit vaccines. Rabies is the oldest known zoonosis which spreads through a neurotropic Lyssavirus primarily mediated through infected canine bites. Rabies causes worldwide loss of more than 60,000 human lives every year. Animal vaccination is equally important to check the transmission of rabies into humans. Rabies oral vaccination can be a good alternative where multiple booster and priming regimens are required while the painful vaccination process can continue for long durations. Introduction of oral vaccines was made to ease the discomfort associated with the mode of introduction of conventional vaccines into the body. Although the rabies oral vaccine can substantially reduce the cost of vaccination in the developing countries, mass immunization programs need larger quantities of vaccines which should be delivered at nominal cost. Expression of recombinant antigen proteins in E. coli is often not viable because of lack of post-translational modifications and folding requirements. Though yeast and insect cell line expression systems have post-translational processing and modifications, significantly different immunological response against their post-translational modification pattern limits their deployment as an expression system. As an alternative, plants are emerging as a promising system to express and deliver wide range of functionally active biopharmaceutical product at lower cost for mass immunization programs. As generation of vaccine antigenic proteins in plant systems are cheaper, the strategy will benefit developing countries where this disease causes thousands of deaths every year. In this chapter, we will discuss about our efforts toward development of oral rabies vaccine and the methodological steps involved during this procedure in detail.

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Mendeley readers

The data shown below were compiled from readership statistics for 20 Mendeley readers of this research output. Click here to see the associated Mendeley record.

Geographical breakdown

Country Count As %
Unknown 20 100%

Demographic breakdown

Readers by professional status Count As %
Researcher 7 35%
Student > Master 4 20%
Lecturer 1 5%
Professor 1 5%
Student > Ph. D. Student 1 5%
Other 2 10%
Unknown 4 20%
Readers by discipline Count As %
Agricultural and Biological Sciences 5 25%
Veterinary Science and Veterinary Medicine 3 15%
Biochemistry, Genetics and Molecular Biology 2 10%
Nursing and Health Professions 2 10%
Medicine and Dentistry 2 10%
Other 2 10%
Unknown 4 20%