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  • 1
    Online Resource
    Online Resource
    Cham :Springer International Publishing AG,
    Keywords: Immunoglobulins. ; Electronic books.
    Type of Medium: Online Resource
    Pages: 1 online resource (316 pages)
    Edition: 1st ed.
    ISBN: 9783030726881
    Language: English
    Note: Intro -- Preface -- Acknowledgements -- Funding Acknowledgements -- Contents -- Contributors -- Part I: Biological Basis of IgY Technology -- 1: Development of IgY Technology: A Historical Perspective -- 1.1 Introduction -- 1.2 Development of IgY Technology -- 1.3 Application of IgY Products at a Glance -- 1.4 Application of the IgY Technology Driven by Legal Regulations in Favour of Animal Protection -- 1.5 Advantages and Limitations Driving IgY Technology -- References -- 2: The Domestic Hen -- 2.1 Introduction -- 2.2 Genetic Selection for Domestic Breeds of Chicken -- 2.3 Breeds of Chicken -- 2.4 Physiology of Chickens -- 2.4.1 Body Temperature -- 2.4.2 Anatomical Structures -- 2.4.3 Crop -- 2.4.4 Cloacal Chamber -- 2.4.5 Medullary Bone -- 2.5 Immune System of the Hen -- 2.5.1 Immune Tissues -- 2.5.1.1 Thymus and Bursa of Fabricius -- 2.5.1.2 Spleen -- 2.5.1.3 Defence System in the Reproductive Organs -- 2.5.1.4 Immune Response -- 2.6 Development of the Reproductive System and Egg Laying -- 2.6.1 Embryology of the Chicken -- 2.6.2 The Ovary -- 2.6.2.1 Follicular Development and Oocyte Maturation -- 2.6.3 Initiation of Laying -- 2.6.4 Reproductive System of the Hen -- 2.6.4.1 Egg Laying and the Oviduct -- 2.7 The Egg -- 2.7.1 Structure of Eggs -- 2.7.2 Composition of Egg Yolk -- 2.8 Concluding Remarks -- References -- 3: Immune Response in Mammals and Chickens -- 3.1 Evolutionary Context -- 3.2 Innate and Adaptive Immune Response -- 3.3 Innate Immune Response in Mammals and Chickens -- 3.3.1 Toll Like Receptors (TLRs) -- 3.3.2 Cytokine Production and Host Defence Peptides -- 3.4 Adaptive Immune Response -- 3.4.1 Lymphoid Tissues in Mammals and Chickens -- 3.4.2 B Cells, T Cells and MHC Class II Proteins -- 3.4.3 Antibody Secretion by B Cells -- 3.5 Genetic Basis for Diversity in Mammalian TCR and Immunoglobulins. , 3.6 Genetic Basis for Diversity in Chicken TCR and Immunoglobulins -- 3.7 Structure of IgG and IgY -- References -- 4: Evolution of Immunoglobulins in Vertebrates -- 4.1 Introduction to Evolution -- 4.2 Immunoglobulin Classes in Vertebrates -- 4.3 Central Position of IgY in Antibody Evolution -- 4.4 Gene Organisation Related to Ig Evolution -- 4.5 Recombination-Activating Gene (RAG)-Mediated Rearrangement -- 4.6 Patterns of V(D)J Rearrangement -- References -- 5: Biology and Molecular Structure of Avian IgY Antibody -- 5.1 The Biology of IgY Production Compared to IgG -- 5.2 Molecular Structure of IgY -- 5.3 Generation of Immunoglobulin Diversity -- 5.4 Differential Expression of IgY Across Species -- 5.5 Generation of IgY(DeltaFc) -- References -- 6: IgY Cell Receptors and Immunity Transfer -- 6.1 Constant Region of Immunoglobulins (Ig) -- 6.2 Transfer of Maternal Immunoglobulins -- 6.3 Transfer of IgY -- 6.3.1 Transfer from the Maternal Circulation to the Yolk of the Oocytes -- 6.3.2 Transfer from the Embryonic Yolk Sac to the Embryonic Blood Stream -- 6.4 IgY Receptor Family -- 6.5 Prospective -- References -- 7: Biorhythms of Hens -- 7.1 Introduction -- 7.2 Observed Rhythms in Hens -- 7.3 Impact of Ageing -- References -- Part II: Core Methods of IgY Technology -- 8: Keeping Laying Hens to Obtain Antibodies -- 8.1 General Introduction -- 8.2 Legislation -- 8.3 Climate, Air Quality, Light and Noise -- 8.4 Enrichment and Nourishment -- 8.4.1 Nest Box -- 8.4.2 Perches -- 8.4.3 Flooring -- 8.4.4 Food and Water -- 8.5 Factors Impacting on IgY Production -- 8.6 Example of a Conventional Housing System -- 8.7 Specific Pathogen Free (SPF) Hens -- 8.8 Specific Pathogen Free (SPF) Avian Facility -- References -- 9: Other Avian Species: Ostrich, Quail, Turkey, Duck and Goose -- 9.1 Introduction -- 9.2 Ostrich Struthio camelus. , 9.3 Japanese Quail Coturnix japonica -- 9.4 Turkey Meleagris gallopavo -- 9.5 Duck Anas platyrhynchos -- 9.6 Goose Anser anser -- 9.7 Summary -- References -- 10: Immunization of Hens -- 10.1 Maintenance of Hens -- 10.2 Source of Antigens -- 10.2.1 Whole Virus or Bacteria -- 10.2.2 Recombinant Proteins -- 10.2.3 Haptens -- 10.2.4 Virus-Like Particles -- 10.2.5 Bacterial Ghosts -- 10.2.6 Virosomes -- 10.2.7 Nucleic Acid Vaccines as Immunogens -- 10.2.8 Vaccine Products as Antigens -- 10.3 Routes of Administration -- 10.4 Amount of Antigen -- 10.5 Adjuvant -- 10.6 Immunization Intervals -- 10.7 Monitoring the IgY Titre -- 10.8 Immunization for the Generation of IgY-scFv -- 10.9 Discussion -- References -- 11: Extraction and Purification of IgY -- 11.1 Introduction -- 11.1.1 Properties of IgY -- 11.1.2 General Considerations for the Extraction of IgY -- 11.2 Egg Collection and Separation of Yolk from Egg White -- 11.3 Delipidation of Egg Yolk -- 11.3.1 Water Dilution -- 11.3.2 Polyethylene Glycol Precipitation -- 11.3.3 Anionic Polysaccharides -- 11.3.4 Organic Solvents -- 11.3.5 Specific Chemicals -- 11.4 Extraction of IgY Following Delipidation -- 11.4.1 Salt Precipitation -- 11.4.2 PEG Precipitation -- 11.4.3 Filtration -- 11.4.4 Aqueous Biphasic Systems (ABS) -- 11.5 Purification of IgY -- 11.5.1 Cation Exchange Chromatography -- 11.5.2 Hydrophobic Charge-Induction Chromatography -- 11.5.3 Affinity Chromatography -- 11.6 Comparison of Methods Used for Delipidation and Extraction of IgY -- 11.7 Commercially Available IgY Extraction Kits -- 11.8 Methods Used to Confirm Purity and Activity of IgY -- 11.8.1 Molecular Weight and Structure -- 11.8.2 Biological Activity of IgY -- 11.9 Purification and Characterization of Monoclonal IgY -- 11.10 The Storage and Stability of IgY Product -- References -- 12: IgY Delivery and Dosage Form -- 12.1 Introduction. , 12.2 Oral Administrations -- 12.3 Parenteral Administrations -- 12.4 IgY in Food and Feed Use -- 12.5 Perspective -- References -- 13: Monoclonal IgY Antibodies -- 13.1 Introduction -- 13.1.1 Monoclonal Antibody and Functional Antibody Fragments -- 13.2 Genetically Engineered Chicken Antibodies -- 13.2.1 Recombinant IgY Fragments -- 13.2.2 Chimeric Antibodies -- 13.2.3 Humanized Antibody -- 13.3 Biomolecular Methods for Monoclonal IgY Generation -- 13.3.1 Hybridoma Technology -- 13.3.2 DT40 Cell Line -- 13.3.3 Antibody Display Technologies -- 13.3.3.1 Phage Display -- 13.3.3.2 Yeast Surface Display -- 13.3.3.3 Ribosomal Display -- 13.3.4 Gel Encapsulated Microenvironment (GEM) Screening Technology -- 13.4 Amino-Acid Synthetic for Monoclonal IgY Generation Antibody Mimetics -- 13.5 Conclusion and Future Prospect -- References -- 14: Protein Production in Transgenic Chickens -- 14.1 Introduction -- 14.2 Protein Production Methods -- 14.3 Advantages of Protein Production in Chicken Egg White -- 14.4 Overview of Chicken Transgenesis -- 14.4.1 Evolution of Delivery Methods and Germline Transmission Frequencies -- 14.4.2 The Effects of Promoters in Protein Expression -- 14.5 Closing Remarks -- References -- Part III: Applications of IgY Technology -- 15: Applications of IgY in Veterinary Medicine -- 15.1 Introduction -- 15.2 Cattle -- 15.2.1 Diarrhoea in Calves -- 15.2.2 Bovine Viral Diarrhoea Virus (BVDV): Prevention and Treatment -- 15.2.3 Mastitis -- 15.3 Pigs -- 15.3.1 Diarrhoea in Pigs -- 15.4 Poultry -- 15.4.1 IgY Treatment of Bacterial Infections of Poultry -- 15.4.2 IgY Treatment of Viral Infections of Poultry -- 15.4.3 IgY Treatment of Protozoan Infections of Poultry -- 15.5 Applications of IgY in Aquaculture -- 15.6 Dogs -- 15.6.1 Canine Parvovirus -- 15.6.2 Canine Morbillivirus -- 15.7 Applications of IgY to Treat Other Animals. , 15.8 Application of IgY Antibodies in Detection and Immunoassay -- 15.8.1 Igy Based Diagnostics of Animal Diseases -- 15.8.2 IgY for Detection of Microbial Contamination in Sea Food -- 15.9 Conclusion and Perspectives -- References -- 16: Applications of IgY in Human Medicine -- 16.1 Introduction -- 16.2 Human Respiratory Infections -- 16.2.1 Severe Acute Respiratory Syndrome Coronaviruses (SARS-CoV) -- 16.2.2 Influenza -- 16.2.3 Hantavirus Pulmonary Syndrome -- 16.2.4 Pseudomonas aeruginosa -- 16.3 Other Human Viral Infections -- 16.3.1 Rabies Virus -- 16.3.2 Emerging Viral Threats -- 16.4 Helicobacter pylori and Gastric Pathogenesis -- 16.5 Mutans Streptococci and Dental Caries -- 16.5.1 Introduction -- 16.5.2 Vaccination Against Dental Caries -- 16.5.3 Passive Immunization -- 16.6 Antitoxin IgY Therapies and Approaches -- 16.6.1 Introduction -- 16.6.2 Escherichia coli -- 16.6.3 Clostridium tetani -- 16.6.4 Clostridium botulinum -- 16.6.5 Clostridium difficile -- 16.6.6 Clostridium perfringens -- 16.6.7 Staphylococcus aureus -- 16.7 Antivenoms -- 16.7.1 Snake Venom -- 16.7.2 Clinical Manifestations of Envenoming -- 16.7.3 IgY Antivenoms: the Key Therapy for Snakebite Envenoming -- 16.7.4 Pharmacological Characterization and Neutralization of Venoms -- References -- 17: IgY Industries and Markets -- 17.1 Introduction -- 17.2 Case-studies of IgY Companies -- 17.2.1 Gentian AS (Moss, Norway) -- 17.2.2 Immunsystem AB (Uppsala, Sweden) -- 17.2.3 Bioinnovo (Castelar, Argentina) -- 17.2.4 Crystal Biosciences (California, USA) -- 17.2.5 Ovagen Group Ltd. -- 17.2.6 ADBioTech (South Korea) -- 17.3 Brief Profiles of Other IgY Companies -- 17.3.1 EW Nutrition (Visbek, Germany) -- 17.3.2 Avianax (North Dakota, USA) -- 17.3.3 IGY Life Sciences (Ontario, Canada) -- 17.3.4 Ostrich Pharma Corp (Kyoto, Japan) -- 17.4 Intellectual Property of IgY. , 17.4.1 IgY: Patenting a Product Already Existing in Nature.
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    Publication Date: 2015-05-15
    Description: A two-dimensional (2D) particle-in-cell simulation is carried out to study the collective effects on the wakefield and stopping power for a hydrogen ion beam pulse propagation in hydrogen plasmas. The dependence of collective effects on the beam velocity and density is obtained and discussed. For the beam velocity, it is found that the collective effects have the strongest impact on the wakefield as well as the stopping power in the case of the intermediate beam velocities, in which the stopping power is also the largest. For the beam density, it is found that at low beam densities, the collective contribution to the stopping power increase linearly with the increase of the beam density, which corresponds well to the results calculated using the dielectric theory. However, at high beam densities, our results show that after reaching a maximum value, the collective contribution to the stopping power starts to decrease significantly with the increase of the beam density. Besides, at high beam densities, the wakefield loses typical V-shaped cone structures, and the wavelength of the oscillation wakefield increases as the beam density increases.
    Print ISSN: 1070-664X
    Electronic ISSN: 1089-7674
    Topics: Physics
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    Publication Date: 2014-09-13
    Description: The plasma screening effects of dense quantum plasmas on charge exchange processes of a fully stripped ion colliding with a hydrogen atom are studied by the classical trajectory Monte Carlo method. The inter-particle interactions are described by the exponential cosine-screened Coulomb potentials. It is found that in weak screening conditions, cross sections increase with the increase of the ionic charge Z . However, in strong screening conditions, the dependence of cross sections on the ionic charge is related to the incident particle energy. At high energies, cross sections show a linear increase with the increase of Z , whereas at low energies, cross sections for Z ≥ 4 become approximately the same. The H e 2 + and C 6 + impacting charge exchange cross sections in dense quantum plasmas are also compared with those in weakly coupled plasmas. The interactions are described by the static screened Coulomb potential. It is found that for both H e 2 + and C 6 + , the oscillatory screening effects of dense quantum plasmas are almost negligible in weak screening conditions. However, in strong screening conditions, the oscillatory screening effects enhance the screening effects of dense quantum plasmas, and the enhancement becomes more and more significant with the increase of the screening parameter and the ionic charge.
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    Topics: Physics
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    Publication Date: 2015-11-20
    Description: The Journal of Organic Chemistry DOI: 10.1021/acs.joc.5b02253
    Print ISSN: 0022-3263
    Electronic ISSN: 1520-6904
    Topics: Chemistry and Pharmacology
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    Publication Date: 2016-04-10
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    Publication Date: 2018-05-01
    Description: The Journal of Organic Chemistry DOI: 10.1021/acs.joc.8b00171
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    Publication Date: 2017-08-17
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