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Animal Defense Systems

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Animal Defense Systems Animal defense systems are based on the distinction between self and nonself. There are two general types of defense mechanisms: – PowerPoint PPT presentation

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Title: Animal Defense Systems


1
Animal Defense Systems
  • Animal defense systems are based on the
    distinction between self and nonself.
  • There are two general types of defense
    mechanisms
  • Nonspecific defenses, or innate defenses, are
    inherited mechanisms that protect the body from
    many different pathogens.
  • Specific defenses are adaptive mechanisms that
    protect against specific targets.

2
Animal Defense Systems
  • White blood cells are important in defense.
  • All blood cells originate from stem cells in the
    bone marrow.
  • White blood cells (leukocytes) are clear and have
    a nucleus and organelles.
  • White blood cells can leave the circulatory
    system.
  • The number of white blood cells sometimes rises
    in response to invading pathogens.

3
Animal Defense Systems
  • There are two main groups of white blood cells
    phagocytes and lymphocytes.
  • Phagocytes engulf and digest foreign materials.
  • Lymphocytes are most abundant. There are two
    types B and T cells.
  • T cells migrate from the circulation to the
    thymus, where they mature.
  • B cells circulate and also collect in lymph
    vessels, and make antibodies.

4
Animal Defense Systems
  • Four groups of proteins play key roles in
    defending against disease
  • Antibodies, secreted by B cells, bind
    specifically to certain substances.
  • T cell receptors are cell surface receptors that
    bind nonself substances on the surface of other
    cells.
  • Major histocompatibility complex (MHC) proteins
    are exposed outside cells of mammals. These
    proteins help to distinguish self from nonself.
  • Cytokines are soluble signal proteins released by
    T cells. They bind and alter the behavior of
    their target cells.

5
Nonspecific Defenses
  • Vertebrate blood contains about 20 antimicrobial
    complement proteins.
  • Complement proteins provide three types of
    defenses
  • They attach to microbes, helping phagocytes
    recognize and destroy them.
  • They activate the inflammation response and
    attract phagocytes to the site of infection.
  • They kill invading cells.

6
Nonspecific Defenses
  • Phagocytes ingest pathogens. There are several
    types of phagocytes
  • Neutrophils attack pathogens in infected tissue.
  • Monocytes mature into macrophages. They live
    longer and consume larger numbers of pathogens
    than do neutrophils. Some roam and others are
    stationary in lymph nodes and lymphoid tissue.
  • Eosinophils kill parasites, such as worms, that
    have been coated with antibodies.
  • Dendritic cells have highly folded plasma
    membranes that can capture invading pathogens.

7
Nonspecific Defenses
  • Natural killer cells are a class of nonphagocytic
    white blood cells
  • They can initiate the lysis of virus-infected
    cells and some tumor cells.

8
Nonspecific Defenses
  • The inflammation response is used in dealing with
    infection or tissue damage.
  • Mast cells and white blood cells called basophils
    release histamine, which triggers inflammation.

9
Specific Defenses The Immune System
  • Four characteristics of the immune system
  • 1. Specificity Antigens are organisms or
    molecules that are specifically recognized by T
    cell receptors and antibodies.
  • The sites on antigens that the immune system
    recognizes are the antigenic determinants (or
    epitopes).
  • Each antigen typically has several different
    antigenic determinants.
  • The host creates T cells and/or antibodies that
    are specific to the antigenic determinants.

10
Specific Defenses The Immune System
  • 2. Diversity
  • It is estimated that the human immune system can
    distinguish and respond to 10 million different
    antigenic determinants.
  • 3. Distinguishing self from nonself
  • Each normal cell in the body bears a tremendous
    number of antigenic determinants. It is crucial
    that the immune system leave these alone.
  • 4. Immunological memory
  • Once exposed to a pathogen, the immune system
    remembers it and mounts future responses much
    more rapidly.

11
Specific Defenses The Immune System
  • The immune system has two responses against
    invaders The humoral immune response and the
    cellular immune response.
  • The two responses operate in concert and share
    mechanisms.

12
Specific Defenses The Immune System
  • The humoral immune response involves antibodies
    that recognize antigenic determinants by shape
    and composition.
  • The cellular immune response is able to detect
    antigens that reside within cells.
  • It destroys virus-infected or mutated cells.
  • Its main component consists of T cells.
  • T cells have T cell receptors that can recognize
    and bind specific antigenic determinants.

13
Specific Defenses The Immune System
  • When the body encounters an antigen for the first
    time, a primary immune response is activated.
  • When the antigen appears again, a secondary
    immune response occurs. This response is much
    more rapid, because of immunological memory.

14
Specific Defenses The Immune System
  • Artificial immunity is acquired by the
    introduction of antigenic determinants into the
    body.
  • Vaccination is inoculation with whole pathogens
    that have been modified so they cannot cause
    disease.
  • Immunization is inoculation with antigenic
    proteins, pathogen fragments, or other molecular
    antigens.
  • Immunization and vaccination initiate a primary
    immune response that generates memory cells
    without making the person ill.

15
B Cells The Humoral Immune Response
  • Antibody molecules are proteins called
    immunoglobulins.
  • Five Classes/Types of IG's.
  • G,M,D,A and E

16
Figure 18.10 Structure of Immunoglobulins (Part
1)
17
Figure 18.11 IgG Antibodies Promote Phagocytosis
18
T Cells The Cellular Immune Response
  • T cells, like B cells, possess specific surface
    receptors.
  • The genes that code for T cell receptors are
    similar to those for immunoglobulins.
  • T cell receptors also have constant and variable
    regions.
  • A major difference between antibodies and T cell
    receptors is that T cell receptors bind only to
    an antigenic determinant that is displayed on the
    surface of an antigen-presenting cell.

19
T Cells The Cellular Immune Response
  • Activated T cells give rise to two types of
    effector cells.
  • Cytotoxic cells, or TC, recognize virus-infected
    cells and kill them by causing them to lyse.
  • Helper T cells, or TH cells, assist both the
    cellular and humoral immune systems.
  • Activated helper T cells proliferate and
    stimulate both B and TC cells to divide.
  • HIV

20
Figure 18.16 The Interaction between T Cells and
Antigen-Presenting Cells (Part 3)
21
Figure 18.15 Macrophages Are Antigen-Presenting
Cells
22
Figure 18.17 (a) Phases of the Humoral and
Cellular Immune Responses (Part 1)
23
Figure 18.17 (a) Phases of the Humoral and
Cellular Immune Responses (Part 2)
24
Figure 18.17 (b) Phases of the Humoral and
Cellular Immune Responses (Part 1)
25
Figure 18.17 (b) Phases of the Humoral and
Cellular Immune Responses (Part 2)
26
T Cells The Cellular Immune Response
  • T cells developing in the thymus are tested to
    ensure that they will be functional and will not
    attack normal self antigens.
  • If the developing T cell binds to one of the
    bodys own normal antigens, it undergoes
    apoptosis.

27
T Cells The Cellular Immune Response
  • For organ transplants to be successful, MHC
    molecules must match otherwise, these same
    molecules will act as antigens.
  • The cellular immune system is responsible for
    rejection.
  • Rejection problems can be controlled somewhat by
    treating patients with immunosuppressing drugs.

28
Disorders of the Immune System
  • The human immune system can overreact to a dose
    of antigen and produce an inappropriate immune
    response. Allergies are the most familiar
    example.
  • Immediate hypersensitivity.
  • Delayed hypersensitivity.
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