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UNIT 6 Immunity (Chapter 21)

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UNIT 6 Immunity (Chapter 21) Immune System Overview Innate Host Defenses Adaptive Defenses (7th edition) NOTE: The following information is based on the Immune System ... – PowerPoint PPT presentation

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Title: UNIT 6 Immunity (Chapter 21)


1
UNIT 6 Immunity (Chapter 21)
  • Immune System Overview
  • Innate Host Defenses
  • Adaptive Defenses

2
NOTE The following information is based on the
Immune System Interactive Physiology tutorials I
highly recommend that you view the interactive
tutorials along with the lecture outline (at the
same time) the following outline is a blending
of the textbook and Interactive Physiology
tutorials
3
Immune System Overview (view the Interactive
Physiology tutorial Immune System Immune System
Overview)
  • There are two major functions of the immune
    system
  • destroy pathogens
  • detect and kill abnormal cells, such as cancerous
    cells
  • Pathogens are classified according to their size
    and where they are located in the body there are
    5 types of pathogens
  • 1. parasitic worms
  • 2. fungi
  • 3. protozoa
  • 4. bacteria
  • 5. viruses
  • viruses are always intracellular (must
    reproduce inside cells), whereas the others are
    usually extracellular parasitic worms are
    macroscopic organisms, whereas the others are
    microorganisms, meaning that they can only be
    seen with a microscope

4
Immune System Overview
  • Line of Defense (fig. 21.1)
  • INNATE DEFENSES (nonspecific defenses)
  • innate external defenses - these are surface
    barriers, such as the skin and mucous membranes
    if the innate external defenses are penetrated
    then the next line of defense is the innate
    internal defenses
  • innate internal defenses - these include cells
    and chemicals in body fluids (e.g. phagocytes and
    NK cells), fever, and inflammation internal
    defenses identify enemies by recognizing markers
    that are unique to the pathogens when they are
    overwhelmed, they secrete chemical messengers to
    mobilize adaptive defenses

5
Immune System Overview
  • Line of Defense (fig. 21.1)
  • ADAPTIVE DEFENSES (specific defenses)
  • differ from innate defenses
  • they are specific (directed against an
    identifiable enemy)
  • they involve B and T lymphocytes
  • they have memory they will recognize an enemy if
    it attacks the body again in the future
  • they are systemic (can act anywhere in the body)
  • B and T lymphocytes recognize pathogens by
    binding to them they recognize antigens of the
    pathogen by shape, also known as the antigenic
    determinant
  • specific B cells called plasma cells secrete
    antibodies, which bind to the antigens

6
Immune System Overview
  • Humoral (antibody-mediated) vs. Cellular
    (cell-mediated) Immunity
  • humoral, or antibody-mediated, immunity is
    directed against pathogens in extracellular
    fluid this immunity involves B lymphocytes and
    antibodies
  • cellular, or cell-mediated, immunity is directed
    against pathogens within the cells this immunity
    involves T lymphocytes for example T cells would
    be activated if a cell has become cancerous or
    attacked by a virus, or if a cell has been
    transplanted from another individual

7
Innate Host Defenses (view the Interactive
Physiology tutorial Immune System Innate Host
Defenses) innate defenses are present at birth
and are genetically determined
  • Innate External Defense System - first line of
    defense
  • surface barriers include the skin and mucous
    membranes of the respiratory, digestive, urinary,
    and reproductive tracts
  • characteristics of skin that help it to resist
    invasion
  • water-resistant and tough keratin outer layer
  • intercellular junctions hold skin cells tightly
    together
  • skin secrections are acidic and have chemicals
    that make the skin inhospitable to pathogens
    e.g. lysozyme destroys cell walls of certain
    bacteria
  • mucous membranes not only provide a barrier, but
    also produce a variety of protective chemicals
    (e.g. lysozyme) and acidic secretions
  • the stomach secretes digestive enzymes and has a
    very low pH
  • the digestive and respiratory pathways are lined
    with sticky mucous that traps pathogens

8
Innate Host Defenses
  • Innate Internal Defense System - second line of
    defense attempts to limit the spread of
    pathogens this system is fast-acting and
    nonspecific
  • the internal defense system has 5 components
  • phagocytic cells (e.g. neutrophils and
    monocytes/macrophages)
  • NK cells (natural killer cells)
  • antimicrobial proteins (complement and
    interferon)
  • inflammation
  • fever

9
Innate Host Defenses
  • Innate Internal Defense System - second line of
    defense attempts to limit the spread of
    pathogens this system is fast-acting and
    nonspecific
  • phagocytes (fig. 21.2)
  • neutrophils are the first cells to leave the
    blood and enter tissues at the sites of infection
    or trauma these cells are short-lived
  • monocytes follow the influx of neutrophils into
    the affected tissue once in the tissue, they
    transform into macrophages they phagocytize many
    more pathogens than neutrophils
  • phagocytes use special membrane receptors to
    recognize and bind molecules that are found on
    pathogens, but not on normal body cells
  • when a phagocyte recognizes a pathogen it
  • - ingests the pathogen
  • - releases chemical alarm signals that mobilize
    other cells of innate and adaptive immunity
  • OPSONIZATION - some bacteria have capsules that
    make it difficult for phagocytes to grab them
    the immune system makes molecules that coat the
    bacteria and enhance phagocytosis this is called
    opsonization both complement and antibodies can
    act as opsonins

10
Innate Host Defenses
  • Innate Internal Defense System - second line of
    defense attempts to limit the spread of
    pathogens this system is fast-acting and
    nonspecific
  • NK cells (natural killer cells)
  • type of lymphocyte involved in innate immunity
  • attack body cells that have been invaded by
    pathogens (e.g. viruses) or cancer they will
    also attack the cells of transplanted tissues
  • NK cells are larger than B and T cells, and
    unlike B and T cells, do not have antigen
    receptors
  • both NK cells and T cells are involved in IMMUNE
    SURVEILLANCE (they continually scan our cells for
    abnormalities)

11
Innate Host Defenses
  • Innate Internal Defense System - second line of
    defense attempts to limit the spread of
    pathogens this system is fast-acting and
    nonspecific
  • antimicrobial proteins
  • interferons (fig. 21.5)- interfere with viral
    replication and activate immune cells cells that
    have been attacked by a virus release interferon
    to help protect neighboring cells that have not
    yet been affected
  • complement (complement system) (fig. 21.6) - it
    complements or enhances other components of
    both innate and adaptive defenses it can mark
    cells for phagocytosis, promote inflammation, and
    kill some bacteria

12
Innate Host Defenses
  • Innate Internal Defense System - second line of
    defense attempts to limit the spread of
    pathogens this system is fast-acting and
    nonspecific
  • inflammation
  • when the body is injured (e.g. a cut, abrasion,
    or bruise) a sequence of events called
    inflammation is initiated
  • tonsillitis, tendonitis, and laryngitis are
    examples of short-lived, or acute, inflammation
    arthritis is an example of long-term, or chronic,
    inflammation
  • there are 4 cardinal signs of inflammation pain,
    swelling, redness, and heat
  • the purpose of inflammation is to bring white
    blood cells and plasma proteins into an injured
    area inflammatory mediators (e.g. histamine from
    basophils and mast cells) cause vasodilation
    (increasing blood flow to the area) and an
    increase in vascular permeability (allowing
    phagocytes and plasma proteins to enter the
    tissue)
  • plasma proteins and more fluid than usual leak
    into the injured area causing EDEMA (increased
    interstitial fluid) edema causes swelling, which
    can contribute to the sensation of pain

13
Innate Host Defenses
  • Innate Internal Defense System - second line of
    defense attempts to limit the spread of
    pathogens this system is fast-acting and
    nonspecific
  • fever
  • generalized increase in body temperature
  • PYROGENS - chemicals secreted by leukocytes and
    macrophages that have been exposed to foreign
    substances in the body they cause the bodys
    thermostat (located in the hypothalamus) to set
    its temperature higher
  • higher body temperatures enhance phagocytosis and
    cause the liver and spleen to sequester iron and
    zinc (making these essential elements less
    available to bacteria) pathogens also do not
    grow very well at higher temperatures

14
Adaptive Defenses - the bodys third line of
defense (view the Interactive Physiology tutorial
Immune System Common Characteristics of B and T
Lymphocytes)
  • Adaptive Defenses are Specific, Systemic, and
    have Memory they include Humoral Immunity
    (antibody-mediated) and Cellular Immunity
    (cell-meditated)
  • B and T Lymphocytes are key players in adaptive
    immunity
  • Antigens (fig. 21.7)
  • have multiple antigenic determinants (based on
    shapes)
  • self-antigens are the shapes that lymphocytes
    expect to find in the body (thus lymphocytes do
    not normally attack them)
  • antigen receptors are specific and diverse

15
Adaptive Defenses
  • Education of Lymphocytes
  • immunocompetence - the lymphocyte is able to
    recognize its one specific antigen by binding to
    it
  • self-tolerance - the lymphocyte is unresponsive
    to self-antigens, so that it does not attack the
    bodys own cells
  • T cells become immunocompetent and self-tolerant
    in the thymus, whereas for B cells this occurs in
    the bone marrow
  • Autoimmune Diseases - lymphocytes attack the
    bodys own cells e.g. Type 1 Diabetes mellitus,
    Graves disease, and Multiple sclerosis
  • Memory Cells - are created in large numbers
    during a primary immune response (exposed to
    antigen for first time) memory cells create a
    larger number of effector cells during a
    secondary immune response (exposed to antigen
    again) thus, the response to the second attack
    will be much greater

16
This concludes the current lecture topic
  • (close the current window to exit the PowerPoint
    and return to the Unit 6 Startpage)
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