Lippincott® Illustrated Reviews: Immunology

Höfundar: Thao Doan; Fabio Lievano; Michelle Swanson-Mungerson; Susan Viselli (Útgáfa: 3)
Lippincott® Illustrated Reviews: Immunology

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Lippincott® Illustrated Reviews: Immunology, 3rd Edition, offers an engaging, vividly illustrated presentation and all of the popular learning features of the Lippincott® Illustrated Review series to reinforce essential immunology concepts and connect basic science to real-life clinical situations. Like other titles in this series, this dynamic resource follows an intuitive outline organization and boasts a wealth of vibrant illustrations and study aids that clarify complex information and ensure retention.

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Útgefandi
Wolters Kluwer Health
ISBN
9781975284015
Print ISBN
9781975172602
Format
ePub
Útgáfa
3
Höfundar
Thao Doan; Fabio Lievano; Michelle Swanson-Mungerson; Susan Viselli
Tungumál
English
Útgefið
2021-04-12
Prent takmörkun á líftíma
10
Prent takmörkun
2
Afritunar takmörkun
2

Kaflar

  • Cover
  • Title Page
  • Copyright
  • Dedication
  • Acknowledgments
  • Reviewers
  • Preface
  • Contents
  • Abbreviations
  • Animations
  • Video 1: B-Cell Activation
  • Video 2: Cytotoxic T-Cell Killing
  • Video 3: Isotype Switch
  • Video 4: T-Cell Activation
  • Video 5: VDJ Light and Heavy
  • Video 6: Type 1 Hypersensitivity
  • Video 7: Type III Hypersensitivity
  • Unit I: Sense of Being: The Concept of Self and Self/Nonself Recognition
  • Chapter 1: The Need for Self-Recognition
  • I. OVERVIEW
  • II. THE IMMUNOLOGIC CONCEPT OF SELF
  • A. Recognizing self
  • B. Recognizing the absence of self
  • C. Recognizing nonself
  • III. IMMUNOLOGIC MEMORY
  • IV. DEFENSE MECHANISMS
  • Study Questions
  • Chapter 2: Antigens and Receptors
  • I. OVERVIEW
  • II. ANTIGENS
  • A. Epitopes: The basic recognition unit
  • B. Immunogens
  • C. Haptens
  • D. Tolerogens
  • E. Immunogenicity
  • III. RECEPTORS
  • A. Preformed receptors
  • B. Somatically generated receptors
  • Study Questions
  • Unit II: The Innate Immune System
  • Chapter 3: Barriers to Infection
  • I. OVERVIEW
  • II. PHYSICAL BARRIERS
  • A. Skin
  • B. Mucous membranes
  • C. Respiratory tract
  • D. Urinary tract
  • III. CHEMICAL AND ENVIRONMENTAL BARRIERS
  • A. pH
  • B. Microcidal action of secreted molecules
  • IV. BIOLOGIC BARRIERS: COMMENSAL MICROBES
  • Study Questions
  • Chapter 4: Cells of the Innate Immune System
  • I. OVERVIEW
  • II. AGRANULAR LEUKOCYTES
  • A. Lymphoid lineage cells
  • B. Monocytic lineage cells
  • III. GRANULAR LEUKOCYTES
  • A. Neutrophils
  • B. Basophils and mast cells
  • C. Eosinophils
  • Study Questions
  • Chapter 5: Innate Immune Function
  • I. OVERVIEW
  • II. RECOGNITION
  • A. Pathogen-associated molecular patterns
  • B. Pattern recognition receptors
  • C. Markers of abnormal self
  • III. SOLUBLE DEFENSE MECHANISMS
  • A. Type I interferons
  • B. Microcidal molecules
  • C. Complement
  • D. Cytokines and chemokines
  • IV. CELLULAR DEFENSE MECHANISMS
  • A. Phagocytosis
  • B. Natural killer cell responses
  • V. INFLAMMATION
  • Study Questions
  • Unit III: The Adaptive Immune System
  • Chapter 6: Molecules of Adaptive Immunity
  • I. OVERVIEW
  • II. IMMUNOGLOBULINS
  • A. Basic structure
  • B. Isotypes
  • III. CLASSICAL PATHWAY OF COMPLEMENT ACTIVATION
  • A. Activation of C1
  • B. Production of C3 convertase
  • C. Production of C5 convertase
  • IV. MAJOR HISTOCOMPATIBILITY MOLECULES
  • A. MHC class I molecules
  • B. MHC class II molecules
  • V. T CELL RECEPTORS
  • A. Basic structure
  • B. Variable and constant regions
  • VI. MOLECULES OF CELLULAR INTERACTION
  • A. Cytokines
  • B. Chemokines
  • C. Adhesion molecules
  • D. Cluster of differentiation molecules
  • E. Signal transduction molecules
  • Study Questions
  • Chapter 7: Cells and Organs
  • I. OVERVIEW
  • II. LYMPHOCYTES
  • A. Thymus-derived cells
  • B. Bone marrow–derived cells
  • C. Natural killer cells
  • III. LYMPHOID TISSUES AND ORGANS
  • A. Primary organs
  • B. Secondary lymphoid tissues and organs
  • C. Lymphatic circulatory system
  • Study Questions
  • Chapter 8: Generation of Immune Diversity: Lymphocyte Antigen Receptors
  • I. OVERVIEW
  • II. PROPERTIES OF LYMPHOCYTE ANTIGEN RECEPTORS
  • III. DNA REARRANGEMENT
  • IV. T CELL RECEPTORS
  • A. Gene clusters encoding T cell receptors
  • B. Variable regions: Rearrangement of V, D, and J genes
  • C. Uniting variable and constant regions
  • D. Random combinations of light and heavy chains
  • V. B CELL RECEPTORS
  • A. Gene clusters encoding B cell receptors
  • B. Light chains
  • C. Heavy chains
  • D. Heavy and light chain combinations
  • E. Isotype switch: Mechanism
  • F. Isotype switch: Consequence
  • G. Somatic hypermutation
  • Study Questions
  • Chapter 9: Lymphocyte Development
  • I. OVERVIEW
  • II. T CELL LINEAGE
  • A. Thymus structure
  • B. αβ T cell development
  • C. γδ T cell development
  • D. NKT cell origin
  • III. B CELL LINEAGE
  • A. Bone marrow
  • B. B cell development
  • C. B-1 and B-2 B cells
  • Study Questions
  • Chapter 10: Lymphocyte Activation
  • I. OVERVIEW
  • II. ANTIGEN PRESENTATION
  • A. Presentation by MHC class II
  • B. Presentation by MHC class I
  • III. T CELL ACTIVATION
  • A. Immunologic synapse
  • B. T cell–signal transduction
  • C. CD41 T cell maturation
  • D. CD8+ T cell maturation
  • E. Control of T cell responses and memory T cell generation
  • IV. B CELL ACTIVATION
  • A. T-independent activation
  • B. T-dependent activation
  • C. Plasma cells and memory B cells
  • Study Questions
  • Chapter 11: Lymphocyte Effector Functions
  • I. OVERVIEW
  • II. HUMORAL IMMUNITY
  • A. Antigen–antibody reactions
  • B. Agglutination
  • C. Neutralization
  • D. Opsonization
  • E. Antibody-dependent cell-mediated cytotoxicity
  • F. Complement activation
  • G. Immediate hypersensitivity
  • III. CELL-MEDIATED IMMUNITY
  • A. Delayed (-type) hypersensitivity: Role of CD41 T cells
  • B. Cytotoxic T lymphocytes: Role of CD8+ T cells
  • IV. IMMUNOLOGIC MEMORY
  • Study Questions
  • Chapter 12: Regulation of Adaptive Responses
  • I. OVERVIEW
  • II. TOLERANCE
  • A. Mechanisms of immunologic nonresponsiveness
  • B. Regulatory T cells
  • C. The role of coinhibitors in immune regulation
  • III. REGULATION OF THE ADAPTIVE IMMUNE RESPONSE BY TH-CELL SUBSETS
  • IV. REGULATORY CYTOKINES
  • Study Questions
  • Unit IV: Clinical Aspects of Immunity
  • Chapter 13: The Well Patient: How Innate and Adaptive Immune Responses Maintain Health
  • I. OVERVIEW
  • II. CELLULAR RECIRCULATION AND HOMING
  • A. Cell adhesion molecules
  • B. Proinflammatory cytokines
  • C. Extravasation
  • III. RESPONSES TO INFECTIOUS AGENTS
  • A. Humoral responses
  • B. Cell-mediated responses
  • C. Effective responses to pathogens
  • D. Microbial evasion of immune responses
  • IV. INFLAMMATION
  • V. MUCOSAL IMMUNITY
  • A. Epithelial layer
  • B. Lamina propria
  • C. Mechanisms of mucosal immunity
  • VI. VACCINATION
  • A. Characteristics of vaccines
  • B. Types of vaccines
  • C. Adjuvants
  • Study Questions
  • Chapter 14: Hypersensitivity Reactions
  • I. OVERVIEW
  • II. TYPE I HYPERSENSITIVITY
  • A. Localized reactions
  • B. Systemic reactions
  • III. TYPE II HYPERSENSITIVITY
  • A. Interaction of antibody with cells
  • B. Interaction of antibody with the extracellular matrix
  • C. Antibody-mediated disruption of cellular function
  • IV. TYPE III HYPERSENSITIVITY
  • A. Localized reactions
  • B. Systemic reactions
  • V. TYPE IV HYPERSENSITIVITY
  • A. Contact dermatitis
  • B. Delayed (-type) hypersensitivity
  • C. T cell–mediated cytotoxicity
  • Study Questions
  • Chapter 15: Immune Deficiency
  • I. OVERVIEW
  • II. PRIMARY (CONGENITAL) IMMUNE DEFICIENCIES
  • A. Defects in stem cells
  • B. Defects in T cells
  • C. Defects in B cells
  • D. Defects in phagocytes and natural killer cells
  • E. Defects in the complement system
  • III. SECONDARY (ACQUIRED) IMMUNE DEFICIENCIES
  • A. Physiologic sequelae
  • B. Therapeutic treatment
  • C. Infection
  • D. Cancer
  • IV. TREATMENT OF IMMUNE DEFICIENCIES
  • A. Passive supplementation
  • B. Bone marrow transplantation
  • C. Genetic engineering
  • Study Questions
  • Chapter 16: Autoimmunity
  • I. OVERVIEW
  • II. SELF-TOLERANCE
  • A. Central tolerance
  • B. Peripheral tolerance
  • III. LOSS OF SELF-TOLERANCE
  • A. Molecular mimicry
  • B. Epitope spreading
  • C. Loss of suppression
  • D. Sequestered antigens
  • E. Neoantigens
  • IV. AUTOIMMUNE DISEASES
  • A. Humoral-associated autoimmune diseases
  • B. Cell-mediated autoimmune diseases
  • V. HLA ASSOCIATION WITH AUTOIMMUNE DISEASES
  • Study Questions
  • Chapter 17: Transplantation
  • I. OVERVIEW
  • II. GENETIC BASIS OF TRANSPLANTATION
  • A. Histocompatibility genes and antigens
  • B. Types of grafts
  • C. The laws of transplantation
  • III. TISSUE REJECTION
  • A. Types of rejection
  • B. Immune responses involved in rejection
  • C. Therapeutic intervention
  • IV. TISSUE-SPECIFIC CONSIDERATIONS
  • A. Transfusion
  • B. Bone marrow
  • C. Immune-privileged sites
  • V. TISSUE SOURCES
  • A. Human tissues and organs
  • B. Nonhuman (xeno-) tissues and organs
  • Study Questions
  • Chapter 18: Immune Pharmacotherapy
  • I. OVERVIEW
  • II. MEASURES THAT ENHANCE THE IMMUNE RESPONSE
  • A. Adjuvant therapy
  • B. Cytokine therapy
  • C. Antibody replacement therapy
  • III. MEASURES THAT DIMINISH THE IMMUNE RESPONSE
  • A. Anti-inflammatory agents
  • B. Immunosuppressive measures
  • IV. THERAPIES USED TO ALTER THE IMMUNE RESPONSE
  • A. Preemptive measures
  • B. Modification of ongoing disease
  • Study Questions
  • Chapter 19: Tumor Immunity
  • I. OVERVIEW
  • II. CANCER
  • A. Terminology and definitions
  • B. Malignant transformation
  • C. Tumors of the immune system
  • D. Oncogenes and cell growth
  • E. Tumor antigens
  • III. IMMUNE SURVEILLANCE
  • A. Innate
  • B. Adaptive
  • IV. IMMUNE EVASION
  • A. Evasion strategies by the tumor
  • B. Tumor immune evasion due to manipulated functions of immune cells
  • V. CANCER IMMUNOTHERAPY
  • A. Use of monoclonal antibodies to target tumor cells
  • B. Immunomodulatory molecules to increase an individual’s inherent antitumor immune response
  • C. Adoptive T cell transfer
  • D. Cancer vaccines
  • E. Alternative approaches to use the immune system to kill tumor cells
  • Study Questions
  • Chapter 20: Measurement of Immune Function
  • I. OVERVIEW
  • II. EPITOPE DETECTION BY ANTIBODIES
  • A. Particulate antigens
  • B. Soluble antigens
  • III. EPITOPE QUANTITATION BY ANTIBODIES
  • A. Radioimmunoassay
  • B. Enzyme-linked immunosorbent assay
  • C. Fluorescent immunosorbent assay
  • IV. EPITOPE DETECTION IN AND ON CELLS
  • A. Immunofluorescence
  • B. Flow cytometry
  • V. ASSESSMENT OF IMMUNE FUNCTION
  • A. Phagocyte function
  • B. Proliferation
  • C. Cytotoxic T-lymphocyte assay
  • VI. ASSESSMENT OF HYPERSENSITIVITY
  • A. Allergy skin testing (type I hypersensitivity)
  • B. Testing for types II and III hypersensitivity
  • C. Contact dermatitis and delayed (-type) hypersensitivity (type IV)
  • Study Questions
  • Review Questions
  • Glossary
  • Index