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The Immune Response
Immunity: Ability of an organism to recognize
and defend itself against specific pathogens or
antigens.
Immune Response: Third line of defense.
Involves pr9oduction of antibodies and
generation of specialized lymphocytes against
specific antigens.
Antigen: Molecules from a pathogen or foreign
organism that provoke a specific immune
response.
The Immune System is the Third Line of
Defense Against Infection
Innate or Genetic Immunity: Immunity an
organism is born with.
Genetically determined.
May be due to lack of receptors or other
molecules required for infection.
 Immunity of mice to poliovirus.
Acquired Immunity:Immunity that an
organism develops during lifetime.
Not genetically determined.
May be acquired naturally or artificially.
 Development of immunity to measles in response to
infection or vaccination.
Types of Acquired Immunity
I. Naturally Acquired Immunity: Obtained in
the course of daily life.
A. Naturally Acquired Active Immunity:
 Antigens or pathogens enter body naturally.
Body generates an immune response to antigens.
Immunity may be lifelong (chickenpox or mumps)
or temporary (influenza or intestinal infections).
B. Naturally Acquired Passive Immunity:
Antibodies pass from mother to fetus via placenta
or breast feeding (colostrum).
No immune response to antigens.
Immunity is usually short-lived (weeks to months).
Protection until child’s immune system develops.
Types of Acquired Immunity (Continued)
II. Artificially Acquired Immunity: Obtained by
receiving a vaccine or immune serum.
A. Artificially Acquired Active Immunity:
 Antigens are introduced in vaccines (immunization).
 Body generates an immune response to antigens.
 Immunity can be lifelong (oral polio vaccine) or temporary
(tetanus toxoid).
B. Artificially Acquired Passive Immunity:
 Preformed antibodies (antiserum) are introduced into body
by injection.
 Snake antivenom injection from horses or rabbits.
 Immunity is short lived (half life three weeks).
 Host immune system does not respond to antigens.
Mechanism of immune responses
6
Active Immunity Passive Immunity
Natural clinical, sub-clinical
infection
via breast milk,
placenta
Artificial Vaccination:
Live, killed, purified
antigen vaccine
immune serum,
immune cells
Duality of Immune System
I. Humoral (Antibody-Mediated) Immunity
 Involves production of antibodies against foreign
antigens.
 Antibodies are produced by a subset of lymphocytes
called B cells.
 B cells that are stimulated will actively secrete
antibodies and are called plasma cells.
 Antibodies are found in extracellular fluids (blood
plasma, lymph, mucus, etc.) and the surface of B cells.
 Defense against bacteria, bacterial toxins, and viruses
that circulate freely in body fluids, before they enter
cells.
 Also cause certain reactions against transplanted
tissue.
Antibodies are Produced by B Lymphocytes
Duality of Immune System (Continued)
II. Cell Mediated Immunity
 Involves specialized set of lymphocytes called T cells
that recognize foreign antigens on the surface of cells,
organisms, or tissues:
 Helper T cells
 Cytotoxic T cells
 T cells regulate proliferation and activity of other cells
of the immune system: B cells, macrophages,
neutrophils, etc.
 Defense against:
 Bacteria and viruses that are inside host cells and are
inaccessible to antibodies.
 Fungi, protozoa, and helminths
 Cancer cells
 Transplanted tissue
Antigens
 Most are proteins or large polysaccharides from
a foreign organism.
 Microbes: Capsules, cell walls, toxins, viral capsids,
flagella, etc.
 Nonmicrobes: Pollen , red blood cell surface
molecules, serum proteins, and surface molecules
from transplanted tissue.
 Lipids and nucleic acids are only antigenic when
combined with proteins or polysaccharides.
 Molecular weight of 10,000 or higher.
Antigens
Epitope:
Small part of an antigen that interacts
with an antibody.
Any given antigen may have several
epitopes.
Each epitope is recognized by a different
antibody.
Epitopes: Antigen Regions that Interact
with Antibodies
Antibodies
 Proteins that recognize and bind to a particular
antigen with very high specificity.
 Made in response to exposure to the antigen.
 One virus or microbe may have several antigenic
determinant sites, to which different antibodies
may bind.
 Each antibody has at least two identical sites
that bind antigen: Antigen binding sites.
 Valence of an antibody: Number of antigen
binding sites. Most are bivalent.
 Belong to a group of serum proteins called
immunoglobulins (Igs).
Antibody Structure
 Monomer: A flexible Y-shaped molecule with
four protein chains:
 2 identical light chains
 2 identical heavy chains
 Variable Regions: Two sections at the end of
Y’s arms. Contain the antigen binding sites
(Fab). Identical on the same antibody, but vary
from one antibody to another.
 Constant Regions: Stem of monomer and lower
parts of Y arms.
 Fc region: Stem of monomer only. Important
because they can bind to complement or cells.
Antibody Structure
18
General antibody Structure
Immunoglobulin Classes
I. IgG
 Structure: Monomer
 Percentage serum antibodies: 80%
 Location: Blood, lymph, intestine
 Half-life in serum: 23 days
 Complement Fixation: Yes
 Placental Transfer: Yes
 Known Functions: Enhances phagocytosis,
neutralizes toxins and viruses, protects fetus and
newborn.
Immunoglobulin Classes
II. IgM
 Structure: Pentamer
 Percentage serum antibodies: 5-10%
 Location: Blood, lymph, B cell surface (monomer)
 Half-life in serum: 5 days
 Complement Fixation: Yes
 Placental Transfer: No
 Known Functions: First antibodies produced
during an infection. Effective against microbes and
agglutinating antigens.
Immunoglobulin Classes
III. IgA
 Structure: Dimer
 Percentage serum antibodies: 10-15%
 Location: Secretions (tears, saliva, intestine, milk),
blood and lymph.
 Half-life in serum: 6 days
 Complement Fixation: No
 Placental Transfer: No
 Known Functions: Localized protection of mucosal
surfaces. Provides immunity to infant digestive
tract.
Immunoglobulin Classes
IV. IgD
 Structure: Monomer
 Percentage serum antibodies: 0.2%
 Location: B-cell surface, blood, and lymph
 Half-life in serum: 3 days
 Complement Fixation: No
 Placental Transfer: No
 Known Functions: In serum function is unknown.
On B cell surface, initiate immune response.
Immunoglobulin Classes
V. IgE
 Structure: Monomer
 Percentage serum antibodies: 0.002%
 Location: Bound to mast cells and basophils
throughout body. Blood.
 Half-life in serum: 2 days
 Complement Fixation: No
 Placental Transfer: No
 Known Functions: Allergic reactions. Possibly
lysis of worms.
How Do B Cells Produce Antibodies?
B cells develop from stem cells in the bone
marrow of adults (liver of fetuses).
After maturation B cells migrate to lymphoid
organs (lymph node or spleen).
Clonal Selection: When a B cell encounters an
antigen it recognizes, it is stimulated and divides
into many clones called plasma cells, which
actively secrete antibodies.
Each B cell produces antibodies that will
recognize only one antigenic determinant.
Clonal Selection of B Cells is Caused by Antigenic
Stimulation
27
Cells of the immune system
Immune system
Myeloid cells
Granulocytic
Neutrophils
Basophils
Eosinophils
Monocytic
Macrophages
Kupffer cells
Dendritic cells
Lymphoid cells
T cells
Helper cells
Suppressor cells
Cytotoxic cells
B cells
Plasma cells
NK cells
Development of the immune system
NK cell
Stem cell
Macrophage
Lymphoid
progenitor
Myeloid
progenitor
T cell
B cell
Plasma Cell
Granulocyte
Monocyte
Mast cell
Dendritic cell
Cells of the immune system: innate
• Phagocytes
• Monocytes/macrophages
• PMNs/neutrophils
• NK cells
• Basophils and mast cells
• Eosinophils
• Platelets
Cells of adaptive immune
response
T cells and B cells
Cells of the immune system: adaptive
• Lymphocytes
• B cells
• Plasma cells (Ab producing)
• T cells
• Cytotoxic (CTL)
• Helper (Th)
• Th1
• Th2
• Th17
• T-reg
Major distinguishing markers
Marker B cell CTL T-helper
Antigen R BCR (surface Ig) TCR TCR
CD3 -- + +
CD4 -- -- +
CD8 -- + --
CD19/ CD20 + -- --
CD40 + -- --
Development of the immune system
NK cell
Stem cell
Macrophage
Lymphoid
progenitor
Myeloid
progenitor
T cell
B cell
Plasma Cell
Granulocyte
Monocyte
Mast cell
Dendritic cell
Bone Marrow Thymus
Tissues
2° Lymphoid

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Immune response.pptx

  • 1. The Immune Response Immunity: Ability of an organism to recognize and defend itself against specific pathogens or antigens. Immune Response: Third line of defense. Involves pr9oduction of antibodies and generation of specialized lymphocytes against specific antigens. Antigen: Molecules from a pathogen or foreign organism that provoke a specific immune response.
  • 2. The Immune System is the Third Line of Defense Against Infection
  • 3. Innate or Genetic Immunity: Immunity an organism is born with. Genetically determined. May be due to lack of receptors or other molecules required for infection.  Immunity of mice to poliovirus. Acquired Immunity:Immunity that an organism develops during lifetime. Not genetically determined. May be acquired naturally or artificially.  Development of immunity to measles in response to infection or vaccination.
  • 4. Types of Acquired Immunity I. Naturally Acquired Immunity: Obtained in the course of daily life. A. Naturally Acquired Active Immunity:  Antigens or pathogens enter body naturally. Body generates an immune response to antigens. Immunity may be lifelong (chickenpox or mumps) or temporary (influenza or intestinal infections). B. Naturally Acquired Passive Immunity: Antibodies pass from mother to fetus via placenta or breast feeding (colostrum). No immune response to antigens. Immunity is usually short-lived (weeks to months). Protection until child’s immune system develops.
  • 5. Types of Acquired Immunity (Continued) II. Artificially Acquired Immunity: Obtained by receiving a vaccine or immune serum. A. Artificially Acquired Active Immunity:  Antigens are introduced in vaccines (immunization).  Body generates an immune response to antigens.  Immunity can be lifelong (oral polio vaccine) or temporary (tetanus toxoid). B. Artificially Acquired Passive Immunity:  Preformed antibodies (antiserum) are introduced into body by injection.  Snake antivenom injection from horses or rabbits.  Immunity is short lived (half life three weeks).  Host immune system does not respond to antigens.
  • 6. Mechanism of immune responses 6 Active Immunity Passive Immunity Natural clinical, sub-clinical infection via breast milk, placenta Artificial Vaccination: Live, killed, purified antigen vaccine immune serum, immune cells
  • 7. Duality of Immune System I. Humoral (Antibody-Mediated) Immunity  Involves production of antibodies against foreign antigens.  Antibodies are produced by a subset of lymphocytes called B cells.  B cells that are stimulated will actively secrete antibodies and are called plasma cells.  Antibodies are found in extracellular fluids (blood plasma, lymph, mucus, etc.) and the surface of B cells.  Defense against bacteria, bacterial toxins, and viruses that circulate freely in body fluids, before they enter cells.  Also cause certain reactions against transplanted tissue.
  • 8. Antibodies are Produced by B Lymphocytes
  • 9. Duality of Immune System (Continued) II. Cell Mediated Immunity  Involves specialized set of lymphocytes called T cells that recognize foreign antigens on the surface of cells, organisms, or tissues:  Helper T cells  Cytotoxic T cells  T cells regulate proliferation and activity of other cells of the immune system: B cells, macrophages, neutrophils, etc.  Defense against:  Bacteria and viruses that are inside host cells and are inaccessible to antibodies.  Fungi, protozoa, and helminths  Cancer cells  Transplanted tissue
  • 10. Antigens  Most are proteins or large polysaccharides from a foreign organism.  Microbes: Capsules, cell walls, toxins, viral capsids, flagella, etc.  Nonmicrobes: Pollen , red blood cell surface molecules, serum proteins, and surface molecules from transplanted tissue.  Lipids and nucleic acids are only antigenic when combined with proteins or polysaccharides.  Molecular weight of 10,000 or higher.
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  • 12. Antigens Epitope: Small part of an antigen that interacts with an antibody. Any given antigen may have several epitopes. Each epitope is recognized by a different antibody.
  • 13. Epitopes: Antigen Regions that Interact with Antibodies
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  • 16. Antibodies  Proteins that recognize and bind to a particular antigen with very high specificity.  Made in response to exposure to the antigen.  One virus or microbe may have several antigenic determinant sites, to which different antibodies may bind.  Each antibody has at least two identical sites that bind antigen: Antigen binding sites.  Valence of an antibody: Number of antigen binding sites. Most are bivalent.  Belong to a group of serum proteins called immunoglobulins (Igs).
  • 17. Antibody Structure  Monomer: A flexible Y-shaped molecule with four protein chains:  2 identical light chains  2 identical heavy chains  Variable Regions: Two sections at the end of Y’s arms. Contain the antigen binding sites (Fab). Identical on the same antibody, but vary from one antibody to another.  Constant Regions: Stem of monomer and lower parts of Y arms.  Fc region: Stem of monomer only. Important because they can bind to complement or cells.
  • 20. Immunoglobulin Classes I. IgG  Structure: Monomer  Percentage serum antibodies: 80%  Location: Blood, lymph, intestine  Half-life in serum: 23 days  Complement Fixation: Yes  Placental Transfer: Yes  Known Functions: Enhances phagocytosis, neutralizes toxins and viruses, protects fetus and newborn.
  • 21. Immunoglobulin Classes II. IgM  Structure: Pentamer  Percentage serum antibodies: 5-10%  Location: Blood, lymph, B cell surface (monomer)  Half-life in serum: 5 days  Complement Fixation: Yes  Placental Transfer: No  Known Functions: First antibodies produced during an infection. Effective against microbes and agglutinating antigens.
  • 22. Immunoglobulin Classes III. IgA  Structure: Dimer  Percentage serum antibodies: 10-15%  Location: Secretions (tears, saliva, intestine, milk), blood and lymph.  Half-life in serum: 6 days  Complement Fixation: No  Placental Transfer: No  Known Functions: Localized protection of mucosal surfaces. Provides immunity to infant digestive tract.
  • 23. Immunoglobulin Classes IV. IgD  Structure: Monomer  Percentage serum antibodies: 0.2%  Location: B-cell surface, blood, and lymph  Half-life in serum: 3 days  Complement Fixation: No  Placental Transfer: No  Known Functions: In serum function is unknown. On B cell surface, initiate immune response.
  • 24. Immunoglobulin Classes V. IgE  Structure: Monomer  Percentage serum antibodies: 0.002%  Location: Bound to mast cells and basophils throughout body. Blood.  Half-life in serum: 2 days  Complement Fixation: No  Placental Transfer: No  Known Functions: Allergic reactions. Possibly lysis of worms.
  • 25. How Do B Cells Produce Antibodies? B cells develop from stem cells in the bone marrow of adults (liver of fetuses). After maturation B cells migrate to lymphoid organs (lymph node or spleen). Clonal Selection: When a B cell encounters an antigen it recognizes, it is stimulated and divides into many clones called plasma cells, which actively secrete antibodies. Each B cell produces antibodies that will recognize only one antigenic determinant.
  • 26. Clonal Selection of B Cells is Caused by Antigenic Stimulation
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  • 28. Cells of the immune system Immune system Myeloid cells Granulocytic Neutrophils Basophils Eosinophils Monocytic Macrophages Kupffer cells Dendritic cells Lymphoid cells T cells Helper cells Suppressor cells Cytotoxic cells B cells Plasma cells NK cells
  • 29. Development of the immune system NK cell Stem cell Macrophage Lymphoid progenitor Myeloid progenitor T cell B cell Plasma Cell Granulocyte Monocyte Mast cell Dendritic cell
  • 30. Cells of the immune system: innate • Phagocytes • Monocytes/macrophages • PMNs/neutrophils • NK cells • Basophils and mast cells • Eosinophils • Platelets
  • 31. Cells of adaptive immune response T cells and B cells
  • 32. Cells of the immune system: adaptive • Lymphocytes • B cells • Plasma cells (Ab producing) • T cells • Cytotoxic (CTL) • Helper (Th) • Th1 • Th2 • Th17 • T-reg
  • 33. Major distinguishing markers Marker B cell CTL T-helper Antigen R BCR (surface Ig) TCR TCR CD3 -- + + CD4 -- -- + CD8 -- + -- CD19/ CD20 + -- -- CD40 + -- --
  • 34. Development of the immune system NK cell Stem cell Macrophage Lymphoid progenitor Myeloid progenitor T cell B cell Plasma Cell Granulocyte Monocyte Mast cell Dendritic cell Bone Marrow Thymus Tissues 2° Lymphoid