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Overview of
Adaptive Immunity
Microbiology and immunology_2
The third line of defense
Overview of Adaptive Immunity
 Adaptive immunity is the body’s ability to recognize and defend
itself against specific pathogens and their products
 Adaptive immunity
 Specificity (acts against specific pathogens)
 Induced (activated in response to specific pathogens)
 Clonality (induced cells proliferate to form clones)
 Self-tolerant (it does not act against self antigens)
 Memory (faster and more effective response to a subsequent
infection caused by the same pathogen)
Adaptive immunity involves the activity of lymphocytes
 Two main types of lymphocytes
 B cells
 T cells
Adaptive Immunity
A resting lymphocyte
 B cells form and mature in
the red bone marrow
 T cells form in the red
bone marrow and mature
in the thymus
 Both B and T cells are found in the blood and lymphoid organs
 Adaptive immunity involves two types of responses
 Humoral immune responses (humoral immunity)
 Activated B cells produce antibodies that function against
extracellular pathogens in the blood
 Cell-mediated immune responses (cellular immunity)
 Activated T cells function against infected host cells
(intracellular pathogens)
 Regulate adaptive immune responses
Adaptive Immunity
Components of adaptive immunity
Lymphatic system
Allows for immune system surveillance
 Lymphatic vessels conduct lymph from tissues and return it to the
circulatory system
 Lymph: fluid leaked from blood vessels into surrounding
tissues
 The lymphatic system includes lymphoid tissues and organs
 Red bone marrow and thymus
 Lymph nodes
 Tonsils, spleen
 Mucosa-associated lymphatic tissue-MALT
Lymphatic
system
 Lymph nodes
are the site of
activation of B cells
and T cells
 Contain
phagocytic cells
(macrophages and
dendritic cells)
Epitopes or antigenic determinants
 Antigens are molecules the
body recognizes as foreign
 Their binding to defensive
cells can trigger adaptive
immune responses
 Antigens are recognized by
the shape of regions called
epitopes
 Microbial antigens include:
Components of the cell walls, capsule, flagella or toxins, proteins and
glycoproteins of viruses, fungi, or protozoa
Exogenous and endogenous
antigens
Clonal deletion
 The body eliminates
lymphocytes that react
against self-antigens
 Lymphocytes that react to
self-antigens undergo
apoptosis
 Leading to the development
of self-tolerance
It is vital that immune responses are not directed
against self-antigens
Humoral response involves activation of B cells
 The precise binding of
the receptor on the B
cell to the epitope
 Determines the
specificity of a humoral
immune response
 All the BCRs on a single B cell are the same
 The binding of the epitope to the BCRs stimulates the B cells to
undergo cell division
 Cell division gives rise to activated B cells called plasma cells
Humoral response involves activation of B cells
 Plasma cells secrete
antibodies or
immunoglobulin (Ig) in the
blood and lymph
 Immunoglobulins have
identical antigen-binding
sites as the BCRs of the
activated B cells
 Y-shaped molecules
with two antigen-
binding sites
 Five classes of
immunoglobulins
 IgG
 IgA
 IgM
 IgE
 IgD
Immunoglobulins
T cells
Cytotoxic T (Tc) cells Kill viral (or other pathogens)
infected host cells
Helper T (Th) cells Help regulate the activities of B
cells and cytotoxic T cells
Regulatory (suppressor) T cells Help prevent autoimmune disease
Cell-mediated immune responses involve T cells
 Immunosystem cytokines act as intercellular signals among all
cell types of the immune system
 Viruses and other intracellular pathogens
 Receptors of T cells are
called TCRs
 TCRs do not recognize
epitopes directly
 TCRs bind epitopes
associated with proteins
called MHC (Major
Histocompatibility
Complex)
T cells allow the body to fight against intracellular
pathogens
MHC - Major Histocompatibility Complex
 MHC proteins hold
and position antigenic
determinants for
presentation to the T
cells
 First identified in graft
patients - determine
compatibility of tissues
for tissue grafting
 Found in the membrane of most cells of vertebrate animals
 APCs
 B cells
 Macrophages
 Dendritic cells
APCs (Antigen presenting cells) and MHC
Dendritic cells typically found in
skin and mucous membranes
 APCs migrate to lymph
nodes where they
present the antigen to
the T cells
 Antigen is bound to
MHC on the surface of
the APCs
 Initiate adaptive immune responses in lymphoid organs –
lymph nodes - where the APCs interact with lymphocytes
 The initial event is the activation of cytotoxic T cells
 Effector cytotoxic T cells will leave the lymph node ready
to attack virally infected cells
The body does not initiate adaptive immune responses at the
site of an infection
Cell-mediated immune responses
Cell-mediated
immune responses
 Interaction
between APC cells, T
helper cells, inactive
cytotoxic T cells,
cytokines
 Leads to activation
of cytotoxic T cells
 Formation of
Memory T cells
Details of the figure will not be part of your
next exam!!!
Cell-mediated immune responses
 Effector cytotoxic T cells will
attack virally infected cells
 Recognize viral epitope on MHC I
of infected cells and
 Induce apoptosis of infected cells
 Memory T cells persist in
lymphoid tissues
 Exposure to the same antigen
will trigger an effective
response called a memory
response
Humoral Immune Responses
 Humoral antibodies are effective against pathogens that
are circulating freely so that the antibody can contact them
 Two types of humoral response
 T-independent humoral immunity
 T-dependent humoral immunity
Humoral immune responses are mounted against exogenous
pathogens
T-independent humoral immune responses
 Occurs without involvement
of helper T cells
 T-independent responses are
reduced in children
 Pathogens with T-
independent antigens can
cause disease in children that
are rare in adults
 Haemophilus influenzae type b (capsule) causes meningitis in
unvaccinated children
Most humoral responses
are of the T-dependent
type
 Interaction between
APC cells, helper T
cells, B cells
 Leads to activation of B
cells plasma cells
will produce antibodies
 Formation of Memory B
cells
 Lymph nodes/cytokines
mediate interactions Details of the figure will not be part of your
next exam!!!
Functions of immunoglobulins
 The binding of antibodies to antigens to form antibody-antigen
complex tags the pathogen/toxins for destruction
 Several mechanisms are involved
 Agglutination by IgG and IgM
 Opsonization
 Neutralization
Functions of immunoglobulins
 Activation of complement
system (classical pathway)
Functions of
immunoglobulins
 Produced by B cell proliferation
 BCRs complementary to antigenic determinant that
triggered their production
 Long-lived cells that persist in the lymphoid tissue
 Initiate antibody secretion if antigen is encountered again
Memory B cells and the establishment of immunological
memory
Immunological Memory
 Primary response occurs after initial contact with an antigen
 Secondary (memory) response occurs after second exposure
 Antibody titer is
the relative amount
of antibodies in
serum
Administration of a tetanus
toxoid in immunization
Subsequent exposure to active
tetanus toxin
Immunological Memory
Colostrum
IgG/IgA
8 2 bio265 microbiology and immunology_2 instructor dr di bonaventura
8 2 bio265 microbiology and immunology_2 instructor dr di bonaventura
8 2 bio265 microbiology and immunology_2 instructor dr di bonaventura

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8 2 bio265 microbiology and immunology_2 instructor dr di bonaventura

  • 1. Overview of Adaptive Immunity Microbiology and immunology_2 The third line of defense
  • 2. Overview of Adaptive Immunity  Adaptive immunity is the body’s ability to recognize and defend itself against specific pathogens and their products  Adaptive immunity  Specificity (acts against specific pathogens)  Induced (activated in response to specific pathogens)  Clonality (induced cells proliferate to form clones)  Self-tolerant (it does not act against self antigens)  Memory (faster and more effective response to a subsequent infection caused by the same pathogen)
  • 3. Adaptive immunity involves the activity of lymphocytes  Two main types of lymphocytes  B cells  T cells Adaptive Immunity A resting lymphocyte  B cells form and mature in the red bone marrow  T cells form in the red bone marrow and mature in the thymus  Both B and T cells are found in the blood and lymphoid organs
  • 4.  Adaptive immunity involves two types of responses  Humoral immune responses (humoral immunity)  Activated B cells produce antibodies that function against extracellular pathogens in the blood  Cell-mediated immune responses (cellular immunity)  Activated T cells function against infected host cells (intracellular pathogens)  Regulate adaptive immune responses Adaptive Immunity
  • 5. Components of adaptive immunity Lymphatic system Allows for immune system surveillance  Lymphatic vessels conduct lymph from tissues and return it to the circulatory system  Lymph: fluid leaked from blood vessels into surrounding tissues  The lymphatic system includes lymphoid tissues and organs  Red bone marrow and thymus  Lymph nodes  Tonsils, spleen  Mucosa-associated lymphatic tissue-MALT
  • 6. Lymphatic system  Lymph nodes are the site of activation of B cells and T cells  Contain phagocytic cells (macrophages and dendritic cells)
  • 7. Epitopes or antigenic determinants  Antigens are molecules the body recognizes as foreign  Their binding to defensive cells can trigger adaptive immune responses  Antigens are recognized by the shape of regions called epitopes  Microbial antigens include: Components of the cell walls, capsule, flagella or toxins, proteins and glycoproteins of viruses, fungi, or protozoa
  • 9. Clonal deletion  The body eliminates lymphocytes that react against self-antigens  Lymphocytes that react to self-antigens undergo apoptosis  Leading to the development of self-tolerance It is vital that immune responses are not directed against self-antigens
  • 10. Humoral response involves activation of B cells  The precise binding of the receptor on the B cell to the epitope  Determines the specificity of a humoral immune response  All the BCRs on a single B cell are the same
  • 11.  The binding of the epitope to the BCRs stimulates the B cells to undergo cell division  Cell division gives rise to activated B cells called plasma cells Humoral response involves activation of B cells  Plasma cells secrete antibodies or immunoglobulin (Ig) in the blood and lymph  Immunoglobulins have identical antigen-binding sites as the BCRs of the activated B cells
  • 12.  Y-shaped molecules with two antigen- binding sites  Five classes of immunoglobulins  IgG  IgA  IgM  IgE  IgD Immunoglobulins
  • 13. T cells Cytotoxic T (Tc) cells Kill viral (or other pathogens) infected host cells Helper T (Th) cells Help regulate the activities of B cells and cytotoxic T cells Regulatory (suppressor) T cells Help prevent autoimmune disease Cell-mediated immune responses involve T cells  Immunosystem cytokines act as intercellular signals among all cell types of the immune system
  • 14.  Viruses and other intracellular pathogens  Receptors of T cells are called TCRs  TCRs do not recognize epitopes directly  TCRs bind epitopes associated with proteins called MHC (Major Histocompatibility Complex) T cells allow the body to fight against intracellular pathogens
  • 15. MHC - Major Histocompatibility Complex  MHC proteins hold and position antigenic determinants for presentation to the T cells  First identified in graft patients - determine compatibility of tissues for tissue grafting  Found in the membrane of most cells of vertebrate animals
  • 16.  APCs  B cells  Macrophages  Dendritic cells APCs (Antigen presenting cells) and MHC Dendritic cells typically found in skin and mucous membranes  APCs migrate to lymph nodes where they present the antigen to the T cells  Antigen is bound to MHC on the surface of the APCs
  • 17.  Initiate adaptive immune responses in lymphoid organs – lymph nodes - where the APCs interact with lymphocytes  The initial event is the activation of cytotoxic T cells  Effector cytotoxic T cells will leave the lymph node ready to attack virally infected cells The body does not initiate adaptive immune responses at the site of an infection Cell-mediated immune responses
  • 18. Cell-mediated immune responses  Interaction between APC cells, T helper cells, inactive cytotoxic T cells, cytokines  Leads to activation of cytotoxic T cells  Formation of Memory T cells Details of the figure will not be part of your next exam!!!
  • 19. Cell-mediated immune responses  Effector cytotoxic T cells will attack virally infected cells  Recognize viral epitope on MHC I of infected cells and  Induce apoptosis of infected cells  Memory T cells persist in lymphoid tissues  Exposure to the same antigen will trigger an effective response called a memory response
  • 20. Humoral Immune Responses  Humoral antibodies are effective against pathogens that are circulating freely so that the antibody can contact them  Two types of humoral response  T-independent humoral immunity  T-dependent humoral immunity Humoral immune responses are mounted against exogenous pathogens
  • 21. T-independent humoral immune responses  Occurs without involvement of helper T cells  T-independent responses are reduced in children  Pathogens with T- independent antigens can cause disease in children that are rare in adults  Haemophilus influenzae type b (capsule) causes meningitis in unvaccinated children
  • 22. Most humoral responses are of the T-dependent type  Interaction between APC cells, helper T cells, B cells  Leads to activation of B cells plasma cells will produce antibodies  Formation of Memory B cells  Lymph nodes/cytokines mediate interactions Details of the figure will not be part of your next exam!!!
  • 23. Functions of immunoglobulins  The binding of antibodies to antigens to form antibody-antigen complex tags the pathogen/toxins for destruction  Several mechanisms are involved  Agglutination by IgG and IgM
  • 24.  Opsonization  Neutralization Functions of immunoglobulins  Activation of complement system (classical pathway)
  • 26.
  • 27.  Produced by B cell proliferation  BCRs complementary to antigenic determinant that triggered their production  Long-lived cells that persist in the lymphoid tissue  Initiate antibody secretion if antigen is encountered again Memory B cells and the establishment of immunological memory
  • 28. Immunological Memory  Primary response occurs after initial contact with an antigen  Secondary (memory) response occurs after second exposure  Antibody titer is the relative amount of antibodies in serum
  • 29. Administration of a tetanus toxoid in immunization Subsequent exposure to active tetanus toxin Immunological Memory