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THE BODY

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chapter 43 the body s defense – PowerPoint PPT presentation

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Title: THE BODY


1
CHAPTER 43
  • THE BODYS DEFENSE

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I. Nonspecific mechanisms
  • Skin Mucous Membranes
  • physical chemical (skin 3-5 pH)
  • saliva, tears mucus perspiration
  • nostril hairs

3
  • Phagocytic White Cells Natural Killer Cells
  • neutrophils cells that become phagocytic in
    infected tissue
  • monocytes become macrophages (phagocytize
    microbes)
  • easinophils against larger invaders (like
    worms)

4
  • Antimicrobial Proteins
  • complement system cause lysis of microbes
  • interferons inhibit viral reproduction
    good against short term made with recombinant
    DNA

5
  • The Inflammatory Response
  • caused when damage to tissue
  • vasodilation increase blood flow redness
    (caused diffusion of fluid edema)
  • chemical signals initiate histamine
    (vasodilation) prostaglandins (increase blood
    flow)
  • migration of phagocytic cells
  • more widespread response can occur in severe
    case (appendicitis)
  • fever due to toxins or leukocytes

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II. Defense of specific invaders
  • Key Features of Immune System
  • Specificity
  • antigen foreign substance that elicits
    immune response
  • antibody antigen-binding proteins
  • Diversity responds to different invaders
  • Memory recognizes previously encountered
    antigens (acquired immunity)
  • Self/Non-Self Recognition

8
  • Active vs. Passive Acquired Immunity
  • active recovery from disease (artificial w/
    vaccine)
  • passive transferred from one individual to
    another (pregnant) temporary

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  • Humoral Immunity Cell-Mediated
  • humoral produce antibodies in response to
    toxins, free bacteria in body fluids
  • cell-mediated intracellular bacteria,
    cancer, transplants (depends on direct action of
    lymphocytes)

14
  • Cell of Immune System
  • 2 main classes of lymphocytes
  • 1. B cells humoral (antibodies)
  • 2. T cells cell-mediated
  • kept in lymph organs

15
III. The immune systems capacity to distinguish
self from nonself is critical in blood
transfusion transplants
  • Blood Groups
  • ABO blood groups nonself recognition
    (antigen present on surface of RBCs not
    antigenic to that person but may be foreign to
    another)
  • A has A antigen make anti-B antibodies

16
  • Blood group antibodies --- agglutinate
  • AB universal recipient
  • O universal donor
  • (not bad for fetus --- these antibodies cant
    cross)

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  • Rh factor
  • - problem when mother is negative baby is
    positive
  • mother makes antibodies when blood crosses
    usually only a problem in 2nd child
  • Rh antibodies can cross placenta destroy
    RBCs of fetus
  • receive anti-Rh antibodies which destroy
    positive red cells before mother develops memory

18
  • Tissue Grafts Organ Transplants
  • MHC (proteins embedded in plasma membranes of
    cells) biochemical fingerprint unique to each
    individual
  • - complicates tissue grafts organ
    transplants

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IV. Abnormal immune function leads to disease
states
  • Autoimmune disease immune system reacts against
    self
  • some cases immune reactions against
    components of own cells lupus
  • rheumatoid arthritis inflammation damages
    cartilage bones in joints
  • destruction of insulin-producing pancreas
    cells insulin-dependent diabetes

20
  • Allergy hypersensitivity of bodys defense to
    environmental antigens (allergen)
  • IgE antibodies recognize pollens as allergens
  • antihistamines used to treat (histamines
    cause dilation increased permeability of small
    blood vessels)

21
  • Anaphylactic shock life-threatening reaction to
    injected antigens (sudden dilation decrease
    blood pressure death in a few minutes)
    epinephrine may be injected

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  • Immunodeficiency
  • individual is inherently deficient in either
    humoral or cell-mediated immune defenses
  • not all inborn Hodgkins disease (cancer
    damages lymphatic) or physical emotional stress
    (adrenal hormones)
  • direct links between nervous immune system

23
  • Acquired Immunodeficiency Syndrome
  • infection from HIV
  • reduction of T cells causes secondary
    infection
  • may remain as a provirus before becoming
    active
  • not eliminated by antibodies because
  • latent provirus, mutate, no T-cells
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