• Fri frakt över 249 kr
  • •
  • Snabba leveranser
  • •
  • Billiga böcker
Kundservice

Du är på sajten för privatpersoner.

Företag, bibliotek eller offentlig verksamhet?

Du handlar på classic.bokus.com, där alla dina funktioner finns intakta.
Till classic.bokus.com
Bokus logotyp. Gå till startsidan.
  • Erbjudanden
  • Nyheter
  • Student
  • Topplistor
  • Barn & ungdom
  • Bokus Play
  • E-böcker
  • Pocketböcker
  • Spel & pussel

10% rabatt på allt med kod: NYSTART10 →

Sidfot

Mina sidor

    Hjälp

    • Kundservice
    • Vanliga frågor och svar
    • Frakt och leverans
    • Retur vid ångerrätt
    • Reklamera vara
    • Betalning
    • Köpvillkor
    • Allmänna villkor
    • Information om webbplatsens tillgänglighet

    Om Bokus

    • Om oss
    • Pressrum
    • För studenter
    • För företag
    • För bibliotek och offentlig verksamhet
    • För leverantörer
    • Hållbarhet

    Populärt

    • Aktuella erbjudanden
    • Presentkort
    • Studentlitteratur
    • Nya böcker
    • Topplistor
    • Signerade böcker
    • Engelska böcker

    Inspiration

    • Boktips
    • BookTok
    • Populära bokserier
    • Barnbokskaraktärer
    • Populära författare
    Logotyp för Bokus
    Följ oss på Facebook (extern länk)Följ oss på Instagram (extern länk)Följ oss på YouTube (extern länk)Följ oss på TikTok (extern länk)
    bokus @ CookiesAnpassa cookiesIntegritetspolicyKöpvillkor
    Till Citymail hemsida (extern länk)Till Budbee hemsida (extern länk)Till Postnord hemsida (extern länk)Till Schenker hemsida (extern länk)Till Early Bird hemsida (extern länk)Till Walleys hemsida (extern länk)
    1. Naturvetenskap och teknik
    2. Teknik och industri
    3. Biokemisk teknik

    Therapeutic Antibody Engineering

    Current and Future Advances Driving the Strongest Growth Area in the Pharmaceutical Industry

    AvWilliam R Strohl,Lila M Strohl

    Inbunden, Engelska, 2012

    Del i serien Woodhead Publishing Series in Biomedicine

    2 741 kr

    Beställningsvara. Skickas inom 10-15 vardagar. Fri frakt över 249 kr.

    Beskrivning

    The field of antibody engineering has become a vital and integral part of making new, improved next generation therapeutic monoclonal antibodies, of which there are currently more than 300 in clinical trials across several therapeutic areas. Therapeutic antibody engineering examines all aspects of engineering monoclonal antibodies and analyses the effect that various genetic engineering approaches will have on future candidates. Chapters in the first part of the book provide an introduction to monoclonal antibodies, their discovery and development and the fundamental technologies used in their production. Following chapters cover a number of specific issues relating to different aspects of antibody engineering, including variable chain engineering, targets and mechanisms of action, classes of antibody and the use of antibody fragments, among many other topics. The last part of the book examines development issues, the interaction of human IgGs with non-human systems, and cell line development, before a conclusion looking at future issues affecting the field of therapeutic antibody engineering.

    • Goes beyond the standard engineering issues covered by most books and delves into structure-function relationships
    • Integration of knowledge across all areas of antibody engineering, development, and marketing
    • Discusses how current and future genetic engineering of cell lines will pave the way for much higher productivity

    Produktinformation

    • Utgivningsdatum:2012-10-16
    • Mått:156 x 234 x undefined mm
    • Vikt:1 190 g
    • Format:Inbunden
    • Språk:Engelska
    • Serie:Woodhead Publishing Series in Biomedicine
    • Antal sidor:696
    • Förlag:Elsevier Science
    • ISBN:9781907568374

    Utforska kategorier

    • Biokemisk teknik inom Naturvetenskap och teknik
    • Biologi inom Naturvetenskap och teknik

    Mer om författaren

    Dr William R. Strohl is Vice President of Biologics Research at Janssen R&D Biotechnology Center of Excellence, and was previously a leader in Merck’s efforts to discover therapeutic monoclonal antibodies, as well as in-licensing of therapeutic targets and technologies associated with monoclonal antibodies. He has over 100 publications and several patents to his credit, and has edited two books.

    Recensioner i media

    "An excellent balance between readability and depth of material.... The book is well referenced and provides plentiful opportunities to continue subject-specific learing." --mAbs Journal"An excellent book describing many aspects of therapeutic antibody generation and the current market share of these drugs. It is an up-to-date evaluation of their production and clinical utility." --Doody's Reviews

    Innehållsförteckning

    • List of figuresList of tablesList of acronyms, abbreviations, and definitionsForewordPrefaceAbout the authorsChapter 1: Introduction to biologics and monoclonal antibodiesAbstract:1.1 Introduction1.2 Definitions of biologies1.3 Recombinant protein therapeutics1.4 MAbs and Fc fusion proteins (FcFPs)1.5 General anatomy of a therapeutic IgG MAb1.6 Naming convention for antibodies from different sourcesChapter 2: Value proposition for therapeutic monoclonal antibodies and Fc fusion proteinsAbstract:2.1 Overview of discovery and development of therapeutic MAbs and FcFPs2.2 Market for MAbs and FcFPs2.3 Currently and recently approved MAbs and FcFPsChapter 3: Antibody structure–function relationshipsAbstract:3.1 Introduction3.2 Constant region structure/function3.3 FAb structure/functionChapter 4: Fundamental technologies for antibody engineeringAbstract:4.1 Introduction4.2 Hybridoma technology – the gateway for therapeutic monoclonal antibodies4.3 Key recombinant DNA technologies4.4 Generation of chimeric antibodies4.5 Display technologies4.6 Maturity timelines for biologies technologiesChapter 5: Sources of antibody variable chainsAbstract:5.1 Human antibody gene organization5.2 Antibody gene rearrangement and diversity in vivo5.3 Sources of antibody diversity5.4 Class-switch recombination5.5 Human variable gene usage5.6 Variable region selection5.7 Variable genes from non-human species5.8 Use of variable genes from humansChapter 6: Variable chain engineering – humanization and optimization approachesAbstract:6.1 Introduction6.2 Chimerization6.3 Humanization6.4 Affinity optimizationChapter 7: Antibody interactions with the immune systemAbstract:7.1 Introduction7.2 Human Fcγ receptors7.3 FcRn and its effect on MAb and FcFP half-life7.4 Other Fc receptors of importance7.5 Complement activationChapter 8: Monoclonal antibody targets and mechanisms of actionAbstract:8.1 Properties of antibody targets8.2 Antibody mechanisms of action8.3 CD20 – example of a target for which multiple MOAs applyChapter 9: Therapeutic antibody classesAbstract:9.1 Human antibody overview9.2 Human IgG isotypes9.3 IgM9.4 IgAChapter 10: Antibody Fc engineering for optimal antibody performanceAbstract:10.1 Antibody engineering for decreased or increased effector function10.2 Current marketed MAbs and clinical candidates with modified Fc10.3 The effect of human Fc polymorphisms on disease and therapeutic index10.4 Fc engineering of IgGs to increase effector function10.5 Fc engineering for silenced effector function10.6 FcγRIIb-dependent suppression of immune response10.7 Antibody engineering for modulation of pharmacokinetics10.8 Tissue targetingChapter 11: IgG glycans and glyco-engineeringAbstract:11.1 Introduction to Fc glycosylation11.2 Non-glycosylated IgGs for lowered effector function11.3 Low- or non-fucosylated oligosaccharides result in higher ADCC11.4 Non-sialylated IgG glycans result in increased ADCC11.5 Sialylated IgG glycans may result in immunosuppressive effects11.6 High-mannose glycoforms11.7 FAb glycosylationChapter 12: Antibody fragments as therapeuticsAbstract:12.1 Introduction to antibody fragments and alternative formats12.2 FAb and scFv antibody fragments12.3 Domain antibodies, including nanobodies, IgNARs, and nanoantibodies12.4 Antibody size and tissue distribution12.5 Strategies for half-life extension of antibody fragments12.5.2 PEGylationChapter 13: Multiple antibody and multi-specificity approachesAbstract:13.1 Introduction13.2 Serum therapy13.3 IVIG13.4 Multi-antibody approaches13.5 Bispecific antibodies based on IgGs13.6 Bispecific antibody fragmentsChapter 14: FcFPs and similar constructs using FcAbstract:14.1 Introduction14.2 Receptor-FcFPs14.3 Traps: multi-ligand binding domains of different receptor chains fused to Fc region14.4 Soluble protein FcFPs14.5 Antibody fragment – Fc fusion proteins14.6 Fc peptide fusions as receptor agonist therapeutics14.7 Other FcFP structures14.8 Issues to consider with FcFPsChapter 15: Antibody-drug conjugatesAbstract:15.1 Introduction to antibody-drug conjugates15.2 Overview and anatomy of a typical ADC15.3 ADC antibodies and targets15.4 ADC chemical “warheads”15.5 ADC linkers15.6 Issues, limitations, and design of ADCs15.7 Radioimmunoconjugates15.8 Protein immunotoxins15.9 ADEPT15.10 Other ADC-like approachesChapter 16: Development issues: antibody stability, developability, immunogenicity, and comparabilityAbstract:16.1 Introduction16.2 Aggregation16.3 Lack of desired solubility16.4 Fragmentation16.5 Post-translational amino acid residue modifications16.6 Instability and isomerization of disulfide bonds16.7 Stability at low pH16.8 Glycosylation issues16.9 Immunogenicity16.10 BiocomparabilityChapter 17: Interactions of human IgGs with non-human systemsAbstract:17.1 Introduction17.2 Non-human primate IgGs and Fcγ receptors17.3 Mouse IgGs and Fcγ receptorsChapter 18: Cell line developmentAbstract:18.1 Introduction18.2 Process summary18.3 Key issues in cell line development18.4 Choice of cell line18.5 Mammalian cell lines18.6 Microbial cells18.7 Multiple cell lines in single batches18.8 Gene and vector optimization and selectable markers18.9 Other industry trendsChapter 19: Issues facing therapeutic monoclonal antibodiesfor the futureAbstract:19.1 Introduction to the future state19.2 Commoditization of the core underlying technologies19.3 Impact of follow-on MAbs and FcFPs19.4 Competition19.5 The continued need for, and limitation of, novel pre-clinically validated targets19.6 Payor pressure19.7 Pipeline in a product concept19.8 Companion diagnostics and patient segmentation19.9 Treatment with multiple antibodies and bispecific antibodies19.10 MAb and FcFP conjugates19.11 Biopharma in 2020 – the focus on BRIC19.12 SWOT analysis of therapeutic MAbs and FcFPs19.13 EpilogueUseful public websites related to antibody engineeringReferencesIndex