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The Concept of Immunity. Immunity : Latin immunis , exempt Susceptibility : Lack of resistance to a disease, also known as Vulnerability Innate immunity : Inborn Adaptive immunity : Acquired, resistance to a specific pathogen. An Overview of the Body’s Defenses.
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The Concept of Immunity • Immunity: Latin immunis, exempt • Susceptibility: Lack of resistance to a disease, also known as Vulnerability • Innate immunity: Inborn • Adaptive immunity: Acquired, resistance to a specific pathogen
An Overview of the Body’s Defenses ANIMATION Host Defenses: The Big Picture Figure 16.1
First Line of Defense: I. Skin & Mucous Membranes • Skin • Keratin, a protective protein • Mucous membranes • Hairs • Cilia • Tears, Saliva, Urine, Vaginal secretions • Lysozyme
Ciliary Escalator Figure 24.7
II. Normal Microbiota • Normal microbiota compete with pathogens for nutrients • Keep pH unfavorable for disease microbes
Differential White Cell Count • Percentage of each type of white cell in a sample of 100 white blood cells • Early and late in infection: Neutrophil then Macrophage
II. Lymphatic SystemTissue + Fluid Figure 16.5a
III. Phagocytosis • Neutrophils • Macrophage • Presents Ag • Secret cytokines (lymphokines + interleukins) Figure 16.6
IV. Inflammation • Releasing histamine • Vasodilation (histamine, kinins, prostaglandins, and leukotrienes) • Redness • Swelling • Pain • Heat • Tissue repair and wall-off
Fever • Abnormally high body temperature • Body’s defensive mechanism • Increase enzyme activity and cytokine activity • Increase blood flow • Some bacteria can not survive at higher temperature • Disadvantage: • Tachycardia • Acidosis • Dehydration • 44–46°C fatal
V. Antimicrobial Substances • Complements C3a + C5a cause inflammation C5b + C6 + C7 + C8 + C9 cause cell lysis
V. Antimicrobial Substances • Interferons • a- and b- interferon: Virus infected cells to produce AVPs • g- interferon: Neutrophils and macrophages • Limitations: • Side effects • Short lived • Only prevents, not stop viral synthesis • No effect on a number of cancers • Ion-binding Proteins • AMPs: Natural antibiotics
Types of Adaptive Immunity • Naturally acquired active immunity • Resulting from infection • Naturally acquired passive immunity • Transplacental or via colostrum • Artificially acquired active immunity • Injection of Ag (vaccination) • Artificially acquired passive immunity • Injection of Ab
Dual Nature of Adaptive Immunity Figure 17.8
Dual Nature of Adaptive Immunity • Humoral immunity: • B-cells • Ag-Ab • Cellular immunity • T-cells • Cytokines ANIMATION Humoral Immunity: Overview
I. Antigens • It has to be large • Ag determinants = epitopes • Haptenand Carrier
Antigens Figure 17.1
Haptens Figure 17.2
II. Antibodies • They are immunoglobulins (Ig) • The antigen-binding sitesrecognize epitope and determine valence • Constant Region / Variable Region • Heavy Chain / Light Chain
Antibodies Figure 17.3a,b
IgG Antibodies • Monomer • Most common and abundant (80%) • Fix complement • Cross placenta • Enhance phagocytosis; neutralize toxins and viruses; protects fetus and newborn • Half-life = 23 days
IgM Antibodies • Pentamer • Agglutination • Fix complement • Agglutinates microbes; first Ab produced in response to infection • Half-life = 5 days
IgA Antibodies • Dimer • 10–15% of serum Abs • In secretions • Mucosal protection • Half-life = 6 days
IgD Antibodies • Monomer • In blood, in lymph, and on B cells • On B cells, initiate immune response • Half-life = 3 days
IgE Antibodies • Monomer • Allergic reactions; lysis of parasitic worms • Half-life = 2 days
III. B Cells • Diversity • Self – non-self discrimination • Memory
1st exposure to Ag First Clones 2nd exposure to Ag
T-independent Activation of B Cells Figure 17.6
T-dependent Activation of B Cells Figure 17.4
Clonal Selection ANIMATION Humoral Immunity: Clonal Selection and Expansion Figure 17.5
Immune Responses to an Antigen Figure 17.16
The Results of Ag-Ab Binding Destroy Made unavailable Figure 17.7
IV. Cellular Immunity • T cells mature in the thymus • Thymic selection eliminates many immature T cells • T cells respond to Ag by T-cell receptors (TCRs) • T cells require antigen-presenting cells (APCs)
T Helper Cells • CD4+ or TH cells (When activated) • Produce cytokines • Help in B cell and Tc cell activation
T Cytotoxic Cells • CD8+or TC cells • Target cells are self carrying endogenous antigens • Activated into cytotoxic T lymphocytes (CTLs) • CTL causes apoptosis
T Cytotoxic Cells Figure 17.11
T Regulatory Cells • Treg cells • CD4 and CD25 on surface • Suppress T cells against self
Antigen-Presenting Cells • Digest antigen • Ag fragments on APC surface with MHC • B cells • Dendritic cells • Activated macrophages ANIMATION Antigen Processing and Presentation: MHC
A Dendritic Cell Figure 17.13
Activated Macrophages Figure 17.14
Natural Killer (NK) Cells • Granular leukocytes destroy cells that don’t express MHC I • Kill virus-infected and tumor cells • Attack parasites