First Line of Defense external barriers to invaders; skin and mucosal membranes

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The immune system is comprised of two systems working together where anything determined to be foreign is deemed harmful - both can work either independently or in concert with one another Innate (nonspecific system) Always on guard, responds within minutes Two branches to this system First Line of Defense external barriers to invaders; skin and mucosal membranes Second Line of Defense if barrier is broken cells and chemicals are called in to attack invaders key aspect to this line of defense is the inflammatory response 1

Adaptive (specific) defense system More like elite fighting core; highly specialized with special weapons specific to the invader Makes up the body s third line of defense Takes considerably longer to respond Works in conjunction with the innate response 2

Innate (Non-specific) Immunity The Immune System First Line of Defense Skin and Mucous Membranes Intact epidermis of the skin and mucous membranes - Skin produces sebum (low ph), lactic acid Lacrimal apparatus, tears mechanically flush the area and contain lyzozyme Saliva mechanical flushing also contains lysozyme Sticky mucous Cilia Flow of urine Defecation and vomiting Gastric juice Vaginal secretions slightly acidic 3

Second Line of Defense Internal Defenses internal antimicrobial proteins, phagocytes, natural killer cells, inflammation, and fever Phagocytes two major types neutrophils and macrophages Five (5) phases of phagocytosis 4

Natural Killer (NK) Cells and Phagocytosis have the ability to kill a wide variety of infectious microbes plus certain spontaneous arising tumor cells Natural Killer Cells 5-10% all lymphocytes in blood (also in spleen, lymph nodes, and red bone marrow Kill cells in two ways» Perforins cause cytolysis» Virus infected or tumor cells, kill by releasing chemicals that cause apoptosis, and phagocytosis of particles 5

Inflammation occurs when cells are damaged in any way Typically characterized by four (4) cardinal signs: Redness Pain Heat Swelling Sometimes loss of function depending upon the site and extent of injury Serves as a protective and defensive mechamism Eliminates microbes, toxins or foreign material from the site Prevents their spread to other organs Prepares the site for tissue repair 6

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Stages of the Inflammatory Response Vasodilation and increased premeability of blood vessels Phagocytic migration Reprair 8

Mediators of Inflammation The Immune System» Histamine vasodilation and increased permeability» Kinins polypeptides - produced from kininogens vasodilation, increased permeability, and chemotaxis» Prostaglandins lipids released by damaged cells enhance histamine and kinins, also aid in emigration» Leukotriens from basophils and mast cells increase permeability, aid adherence of phagocytes and pathogens, and chemotaxis» Complement enhance histamine, neutrophilic chemotaxis, promote phagocytosis, and in some cases can kill bacteria directly After phagocytosis the phagocytes die and along with damaged tissue and fluid form pus if the pus accumulates and abcess forms 9

Antimicrobial Proteins Interferons» produced by virus infected cells, diffuse to uninfected neighboring cells prevents viral replication in those cells by blocking protein synthesis» Enhance the activity of phagocytes and natural killer (NK) cells» Inhibit cell growth» Suppress tumor formation 10

Complement System a group of blood proteins that when activated enhance certain immune, allergic and inflammatory reactions 11

» Classical Pathway requires an antibody and antigen to form a complex to initiate the path» Alternate Pathway requires certain polysacharrides on the surface of some microbes to initiate the path» Both pathways lead to the formation of membrane attack complex (MAC) that opens a channel in the microbe and kills it Transferrins proteins that bind with iron, inhibiting the amount of iron needed by some bacteria 12

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Fever usually caused by an infection from bacteria and their toxins or viruses Inhibits microbial growth by sequestering iron, and zinc needed by bacteria Speeds up metabolism for repair Adaptive Defenses (Specific Resistance : Immunity) involves the production of specific lymphocytes or antibodies against a specific antigen Three important aspects Specificity Systemic Possesses memory 14

Types of Immune Responses The Immune System Cell-Mediated Immunity (CMI) the destruction of antigens by T cells, always involves cells attacking cells particularly effective against: Fungi Parasites Viruses Some cancer cells Foreign tissue transplants Antibody-Mediated (Humoral) Immunity (AMI) refers to the destruction of antigens by antibodies - works against: Antigens dissolved in body fluids Extracellular pathogens * Often a pathogen can provoke both types of immune response 15

Antigens chemical substances that are recognized as foreign (nonself) by antigen receptors when introduced into the body Made up of large, complex molecules Most often proteins Nucleoproteins Lipoproteins Glycoproteins Certain large polysaccharides Partial antigens (haptens) are only reactive if attached to larger molecules 16

Complete Antigens and Haptens Complete antigens possess two important properties» Immunogenicity» Reactivity Hapten (Incomplete Antigen)» Not immunogenic by themselves» Bind with larger molecules and can become immunogenic» Posses the property of reactivity but lack immunogenicity 17

Antigenic Determinants The Immune System 18

Self-Antigens: MHC Proteins The Immune System Major Histocompatability Complex (MHC) Antigens are unique to each persons cells Are associated with self-antigens, aid in the detection of foreign invaders All cells except RBC s display MHC class I antigens Some cells also display MHC class II antigens More in a bit 19

Cells of the Adaptive Immune System Lymphocytes T and B Cells Both are derived from the bone marrow T cells complete their maturation in the thymus gland, where they become immunocompetent B cell gain the immunocompetence in the red bone marrow Before leaving either the bone marrow or thymus gland B and T cells acquire distinctive surface antigen receptors 20

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Antigen-Presenting Cells (APCs) Present exogenous antigens together with MHC II molecules to T cells; antigen presenting cells include: Dendritic Cells connective tissues Langerhan s Cells - skin Macrophages B cells 22

Antibody-Mediated (Humoral) Immunity (AMI) involves B cells and the production of antibodies 23

Immunological Memory The Immune System 24

Active and Passive Immunity The Immune System 25

Antibodies Proteins that can combine specifically with antigenic determinants on the antigen that caused their production Are composed of heavy (H) and light (L) chains, each of which has a variable and constant portion 26

Antibody Classes 27

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Cell-Mediated Immunity involves T cells, which can be of varying types: Helper T (T4) cells Display CD4 protein Recognize foreign fragments associated with MHC II molecules Secrete several cytokines, especially interleukin-2 that is a costimulator of helper T cells, cytotoxic T cells and B Cells Cytotoxic T ([Killer], [Tc], [T8]) cells Display CD8 protein Recognize antigen fragments associated with MHC I molecules Suppressor T cells (T s ) Gamma delta T cells (T gd ) bind with MHC I type antigens found typically on tumor cells 29

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"From Goldberg, S., 'Clinical Physiology Made Ridiculously Simple'; MedMaster, 2004" 35

Elimination of Invaders two methods Production of perforin, results in destruction of cell via cytolysis Production of lymphotoxin cell s DNA is disrupted resulting in cell s death 36

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Organ Transplants and Prevention of Rejection Autographs Isographs Allographs Xenographs Immunosuppressive Therapy Corticosteroids Antiproliferative Drugs Immunosuppressant drugs 38

Be sure to look over Homeostatic Imbalances of Immunity pages 818 822 and A Closer Look pages 822-823 There will not be many questions on the exam If you understand the material presented in chapter 21 you should be able to understand the explanations of these disorders I suggest that you review them on your own and if you have any questions be sure to ask me to help explain the conditions presented 39