Adaptive(Acquired)
Immune Response
By
Prof. S.B Zailani
Chief Consultant Clinical Microbiologist
Strategy of Adaptive
Immune Response
 First response to particular antigen called
primary response
 May take a week or more to develop
 Immune system remembers pathogen on
subsequent exposure
 Termed secondary response
 Adaptive immunity divided into
 Humoral immunity
 Eliminates extracellular pathogens
 Cellular immunity
 Eliminates intracellular pathogens
Strategy of Adaptive
Immune Response
 Overview of humoral immunity
 Mediated by B lymphocytes
 B cells
 Develops in bone marrow
 B cells may be triggered to proliferate into plasma
cells
 Plasma cells produce antibodies
 Antibodies produce when antigen binds B cell receptor
 Some B cells produce memory cells
Strategy of Adaptive
Immune Response
Strategy of Adaptive
Immune Response
 Overview of cellular immunity
 Mediated by T lymphocytes
 T cells
 Matures in thymus
 Divided into 2 subsets
 Cytotoxic T cells
 Helper T cells
 T cell receptors help with antigen recognition
Anatomy of the Lymphoid System
 Lymphoid system collection of tissues and
organs designed to bring B and T cells in
contact with antigens
 In order for body to mount appropriate response,
immune cells must encounter antigen
 Lymphoid system includes
 Lymphatic vessels
 Secondary lymphoid organs
 Primary lymphoid organs
Anatomy of the Lymphoid System
Anatomy of the Lymphoid System
 Lymphatic vessels
 Carry lymph to body tissues
 Lymph formed as result of body’s circulatory system
 Lymph travels through vessels to lymph
nodes
 Material such as protein is removed
 Fluid portion empties back into blood stream
Anatomy of the Lymphoid System
 Primary lymphoid organs
 Bone marrow and thymus are primary lymphoid
organs
 Location where stem cells destined to become B and T
cells mature.
 B cells mature in bone marrow
 T cells mature in thymus
 Once mature, cells leave primary lymphoid organs and
migrate to secondary lymphoid organs
Anatomy of the Lymphoid System
 Secondary lymphoid organs
 Sites where lymphocytes gather to encounter
antigens; organs include
 Lymph nodes
 Spleen
 Tonsils
 Adenoids
 Appendix
 Organs situated strategically
 Allows for initiation of immune response from nearly
any place in body
Clonal Selection
of Lymphocytes
 Lymphocyte characteristics include:
› Immature
 Antigen specific receptors not fully developed
› Naive
 Have antigen receptor but have not encountered antigen
› Activated
 Able to proliferate
 Have bound antigen
› Effectors
 Descendents of activated lymphocytes
 Able to produce specific cytokines
 Plasma cells, T helper and cytotoxic T cells effector cells
› Memory lymphocytes
 Long-lived descendents of activated lymphocytes
 Memory cells responsible for seed and effectiveness of
secondary response
 Remembers antigen on subsequent exposure
B Lymphocyte and
Antibody Response
 Antigen binds to B cell receptor
 Poises B cell to respond
 In many cases B cell needs confirmation from helper T cells
 Ag enters the body and is phagocytozed and processed by
macrophages
 These macrophages destroy Ag and present a portion on the
surface of the macrophage next to self Ag
 Macrophages are called antigen-presenting cells (APC)
 Processed Ag combines with specific TH with the appropriate
receptor
 APC releases substances to activate TH cell
 TH cell activates B cells to divide and differentiate
› Produce plasma cells and memory B cells
B Lymphocyte and
Antibody Response
B Lymphocyte and Antibody Response
 Characteristic of primary response
 Lag period of 10 to 12 days occurs before antibody
detection in blood
 Activated B cells proliferate and differentiate into increasing
numbers of plasma cells as long as antigen is present
 Net result is slow steady increase in antibody titer
B Lymphocyte and
Antibody Response
 Class switching
 B cells initially programmed to differentiate into plasma cells
 Plasma cells secrete IgM antibodies
 Helper T cells produce cytokines
 Some B cells switch programming
 Differentiate to plasma cells that secrete other classes of
antibodies
 Commonly IgG
B Lymphocyte and
Antibody Response
 Formation of memory
 B cells that have undergone class switching
 Produce IgG antibody
 IgG is antibody of memory
 IgG antibody can circulate in body for years allowing
protection against specific antigens
B Lymphocyte and
Antibody Response
 Characteristics of secondary response
 Memory cells responsible for swift effective
reaction of secondary response
 Often eliminate invaders before noticeable harm is
done
 Vaccine exploits phenomenon of immunologic
memory
 Some memory B cells will differentiate into
plasma cells
 Results in rapid production of antibodies
T Lymphocytes
Antigen Recognition and Response
 General characteristics of T cells
 Have multiple copies of T cell
receptors
 Receptors have variable sites of
antigen binding
 Role of T cells different from B cells
 T cells never produce antibodies
 T cells armed with effectors that
interact directly with antigen
 T cell receptor does not react with
free antigen
 Antigen must be presented by
APC
T Lymphocytes
Antigen Recognition and Response
 General Characteristics
 During antigen presentation, antigen cradled in
grove of major histocompatability complex
molecule (MHC molecule)
 Two types MHC
 MHC class I
 Bind endogenous antigen
 MHC class II
 Bind exogenous antigen
T Lymphocytes
Antigen Recognition and Response
 General characteristics
 Two major function T cell populations
 Cytotoxic T cells
 Proliferate and differentiate to destroy infected or
cancerous “self” cells
 Have CD8 marker
 Recognize MHC class I
 Helper T cells
 Multiply and develop into cells that activate B cells and
macrophages
 Stimulate other T cells; orchestrate immune response
 Have CD4 marker
 Recognize antigen display by MHC class II
T Lymphocytes
Antigen Recognition and Response
 Functions of Tc (CD8) cells
 Induce apoptosis in “self” cells
 Cells infected with virus or intracellular
microbe
 Destroys cancerous “self” cells
 Nucleated cells degrade portion of
proteins
 Load peptides into groove of MHC class I
molecule
 MHC class I molecule recognized by
circulating Tc cell
 Cell destroyed by lethal effector function of Tc
cell
 Tc cells releases pre-formed cytokines to
destroy cell
T Lymphocytes
Antigen Recognition and Response
 Functions of TH (CD4) cells
 Orchestrate immune response
 Recognize antigen presented by MHC class II molecules
 MHC class II molecules found only on APC
 If TH cell recognizes antigen, cytokines are delivered
 Cytokines activate APC to destroy antigen
T Lymphocytes
Antigen Recognition and Response
 Role of TH cells in B cell activation
 If TH cell encounters B cell bearing peptide: MHC
class II complex
 TH cell responds by producing cytokines
 B cell is activated in response to cytokine
stimulation
 B cell proliferates and undergoes class switching
 Also drives formation of B memory cells
T Lymphocytes
Antigen Recognition and Response
 Role of TH cells in macrophage
activation
 Macrophages routinely engulf
invading microbes resistant to
lysosomal killing
 TH cells recognize macrophage with
engulfed microbes resistant to
killing
 TH cells activate macrophages by
delivering cytokines that induce
more potent destructive
mechanisms
Natural Killer Cells
 Natural killer cells descend from lymphoid
stem cells
› They lack antigen specificity
 No antigen receptors
 Recognize antigens by means of Fc portion of IgG
antibodies
 Allow NK cells to attach to antibody-coated cells
 Actions augment adaptive immune response
› Important in process of antibody dependent
cellular toxicity
 Enable killing of host cells with foreign protein in
membrane
 Natural killer cells recognize destroyed host
cells with no MHC class I surface molecules
› Important in viral infection
Lymphocyte Development
 During lymphocyte development, B and T cells
acquire ability to recognize distinct epitopes
 Once committed to specific antigen, cells “checked
out” to ensure proper function
 B cells undergo developmental stages in bone
marrow
 T cells go through process in thymus
Active immunity Passive immunity
 1, Need active participation
of self immune system.
 2, Acquisition:-
i, natural disease process
ii, vaccination(killed or live)
iii, toxoid
 3.Effectiveness:- High
 4. Time required to
develop: 5 to 14 days
 1. It does not
 2.
i)Passing of IgG
vertically
ii)Injection of
readymade antibodies
 3. low
 4. Immediately
Active immunity Passive immunity
 5.Duration of
effectiveness:-
Longer (months-
years)
 6.Reactivation:-
By giving booster
dose
 7.Use:-
prophylaxis
 5. Days to weeks
 6. No reactivation
 7.Prophylaxis and
Therapy
Summary of Adaptive Immune Response
Thank You for Listening

ADAPTIVE IMMUNITY LECTURE easy understanding pptx

  • 1.
    Adaptive(Acquired) Immune Response By Prof. S.BZailani Chief Consultant Clinical Microbiologist
  • 2.
    Strategy of Adaptive ImmuneResponse  First response to particular antigen called primary response  May take a week or more to develop  Immune system remembers pathogen on subsequent exposure  Termed secondary response  Adaptive immunity divided into  Humoral immunity  Eliminates extracellular pathogens  Cellular immunity  Eliminates intracellular pathogens
  • 3.
    Strategy of Adaptive ImmuneResponse  Overview of humoral immunity  Mediated by B lymphocytes  B cells  Develops in bone marrow  B cells may be triggered to proliferate into plasma cells  Plasma cells produce antibodies  Antibodies produce when antigen binds B cell receptor  Some B cells produce memory cells
  • 4.
  • 5.
    Strategy of Adaptive ImmuneResponse  Overview of cellular immunity  Mediated by T lymphocytes  T cells  Matures in thymus  Divided into 2 subsets  Cytotoxic T cells  Helper T cells  T cell receptors help with antigen recognition
  • 7.
    Anatomy of theLymphoid System  Lymphoid system collection of tissues and organs designed to bring B and T cells in contact with antigens  In order for body to mount appropriate response, immune cells must encounter antigen  Lymphoid system includes  Lymphatic vessels  Secondary lymphoid organs  Primary lymphoid organs
  • 8.
    Anatomy of theLymphoid System
  • 9.
    Anatomy of theLymphoid System  Lymphatic vessels  Carry lymph to body tissues  Lymph formed as result of body’s circulatory system  Lymph travels through vessels to lymph nodes  Material such as protein is removed  Fluid portion empties back into blood stream
  • 10.
    Anatomy of theLymphoid System  Primary lymphoid organs  Bone marrow and thymus are primary lymphoid organs  Location where stem cells destined to become B and T cells mature.  B cells mature in bone marrow  T cells mature in thymus  Once mature, cells leave primary lymphoid organs and migrate to secondary lymphoid organs
  • 11.
    Anatomy of theLymphoid System  Secondary lymphoid organs  Sites where lymphocytes gather to encounter antigens; organs include  Lymph nodes  Spleen  Tonsils  Adenoids  Appendix  Organs situated strategically  Allows for initiation of immune response from nearly any place in body
  • 12.
    Clonal Selection of Lymphocytes Lymphocyte characteristics include: › Immature  Antigen specific receptors not fully developed › Naive  Have antigen receptor but have not encountered antigen › Activated  Able to proliferate  Have bound antigen › Effectors  Descendents of activated lymphocytes  Able to produce specific cytokines  Plasma cells, T helper and cytotoxic T cells effector cells › Memory lymphocytes  Long-lived descendents of activated lymphocytes  Memory cells responsible for seed and effectiveness of secondary response  Remembers antigen on subsequent exposure
  • 13.
    B Lymphocyte and AntibodyResponse  Antigen binds to B cell receptor  Poises B cell to respond  In many cases B cell needs confirmation from helper T cells  Ag enters the body and is phagocytozed and processed by macrophages  These macrophages destroy Ag and present a portion on the surface of the macrophage next to self Ag  Macrophages are called antigen-presenting cells (APC)  Processed Ag combines with specific TH with the appropriate receptor  APC releases substances to activate TH cell  TH cell activates B cells to divide and differentiate › Produce plasma cells and memory B cells
  • 14.
  • 15.
    B Lymphocyte andAntibody Response  Characteristic of primary response  Lag period of 10 to 12 days occurs before antibody detection in blood  Activated B cells proliferate and differentiate into increasing numbers of plasma cells as long as antigen is present  Net result is slow steady increase in antibody titer
  • 16.
    B Lymphocyte and AntibodyResponse  Class switching  B cells initially programmed to differentiate into plasma cells  Plasma cells secrete IgM antibodies  Helper T cells produce cytokines  Some B cells switch programming  Differentiate to plasma cells that secrete other classes of antibodies  Commonly IgG
  • 17.
    B Lymphocyte and AntibodyResponse  Formation of memory  B cells that have undergone class switching  Produce IgG antibody  IgG is antibody of memory  IgG antibody can circulate in body for years allowing protection against specific antigens
  • 18.
    B Lymphocyte and AntibodyResponse  Characteristics of secondary response  Memory cells responsible for swift effective reaction of secondary response  Often eliminate invaders before noticeable harm is done  Vaccine exploits phenomenon of immunologic memory  Some memory B cells will differentiate into plasma cells  Results in rapid production of antibodies
  • 19.
    T Lymphocytes Antigen Recognitionand Response  General characteristics of T cells  Have multiple copies of T cell receptors  Receptors have variable sites of antigen binding  Role of T cells different from B cells  T cells never produce antibodies  T cells armed with effectors that interact directly with antigen  T cell receptor does not react with free antigen  Antigen must be presented by APC
  • 20.
    T Lymphocytes Antigen Recognitionand Response  General Characteristics  During antigen presentation, antigen cradled in grove of major histocompatability complex molecule (MHC molecule)  Two types MHC  MHC class I  Bind endogenous antigen  MHC class II  Bind exogenous antigen
  • 21.
    T Lymphocytes Antigen Recognitionand Response  General characteristics  Two major function T cell populations  Cytotoxic T cells  Proliferate and differentiate to destroy infected or cancerous “self” cells  Have CD8 marker  Recognize MHC class I  Helper T cells  Multiply and develop into cells that activate B cells and macrophages  Stimulate other T cells; orchestrate immune response  Have CD4 marker  Recognize antigen display by MHC class II
  • 22.
    T Lymphocytes Antigen Recognitionand Response  Functions of Tc (CD8) cells  Induce apoptosis in “self” cells  Cells infected with virus or intracellular microbe  Destroys cancerous “self” cells  Nucleated cells degrade portion of proteins  Load peptides into groove of MHC class I molecule  MHC class I molecule recognized by circulating Tc cell  Cell destroyed by lethal effector function of Tc cell  Tc cells releases pre-formed cytokines to destroy cell
  • 23.
    T Lymphocytes Antigen Recognitionand Response  Functions of TH (CD4) cells  Orchestrate immune response  Recognize antigen presented by MHC class II molecules  MHC class II molecules found only on APC  If TH cell recognizes antigen, cytokines are delivered  Cytokines activate APC to destroy antigen
  • 24.
    T Lymphocytes Antigen Recognitionand Response  Role of TH cells in B cell activation  If TH cell encounters B cell bearing peptide: MHC class II complex  TH cell responds by producing cytokines  B cell is activated in response to cytokine stimulation  B cell proliferates and undergoes class switching  Also drives formation of B memory cells
  • 25.
    T Lymphocytes Antigen Recognitionand Response  Role of TH cells in macrophage activation  Macrophages routinely engulf invading microbes resistant to lysosomal killing  TH cells recognize macrophage with engulfed microbes resistant to killing  TH cells activate macrophages by delivering cytokines that induce more potent destructive mechanisms
  • 26.
    Natural Killer Cells Natural killer cells descend from lymphoid stem cells › They lack antigen specificity  No antigen receptors  Recognize antigens by means of Fc portion of IgG antibodies  Allow NK cells to attach to antibody-coated cells  Actions augment adaptive immune response › Important in process of antibody dependent cellular toxicity  Enable killing of host cells with foreign protein in membrane  Natural killer cells recognize destroyed host cells with no MHC class I surface molecules › Important in viral infection
  • 27.
    Lymphocyte Development  Duringlymphocyte development, B and T cells acquire ability to recognize distinct epitopes  Once committed to specific antigen, cells “checked out” to ensure proper function  B cells undergo developmental stages in bone marrow  T cells go through process in thymus
  • 28.
    Active immunity Passiveimmunity  1, Need active participation of self immune system.  2, Acquisition:- i, natural disease process ii, vaccination(killed or live) iii, toxoid  3.Effectiveness:- High  4. Time required to develop: 5 to 14 days  1. It does not  2. i)Passing of IgG vertically ii)Injection of readymade antibodies  3. low  4. Immediately
  • 29.
    Active immunity Passiveimmunity  5.Duration of effectiveness:- Longer (months- years)  6.Reactivation:- By giving booster dose  7.Use:- prophylaxis  5. Days to weeks  6. No reactivation  7.Prophylaxis and Therapy
  • 30.
    Summary of AdaptiveImmune Response
  • 31.
    Thank You forListening