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IMMUNE SYSTEMBy :
Cici Rizky Y 120210103016
Adha Qiftiyatul M 120210103020
Wulan Anggraeni 120210103048
Tesa Lusidyah 120210103052
What is the immune system?
 The body’s defense against disease causing organisms, malfunctioning cells,
and foreign particles
IMMUNE SYSTEM
Adaptive Immune System
(Specific respon)
Innate Immune system
(Non specific respon)
Disorders and
disease
External
Defense
Internal
Defense
-Skin
-Mucous
membranes
-secretorions
-Phagocytic cells
-Antimicrobial
subtance
-Inflammatory
response
-Natural killer cells
Limfosit T Limfosit B
Immune System : 2 branches
1. The Innate Immune system =
- is present before any exposure to pathogens and is effective
from the time of birth
2. The Adaptive Immune System =
- develops after exposure to agents such as microbes, toxins, or
other foreign substances
INNATE IMMUNITY
 Innate immunity is present before any exposure to
pathogens and is effective from the time of birth
 It involves nonspecific responses to pathogens
 Innate immunity consists of external barriers plus internal
cellular and chemical defenses
Nonspecific response
 Skin
 Mucous membranes
 Secretions
EXTERNAL INNATE IMMUNITY
- Phagocytic cells
There are different types of
phagocytic cells:
- Neutrophils engulf and destroy
microbes
- Macrophages are part of the
lymphatic system and are found
throughout the body
- Eosinophils discharge
destructive enzymes
- Dendritic cells stimulate
development of acquired
immunity
Pseudopodia
surround
microbes.
1
Microbes
are engulfed
into cell.
2
Vacuole
containing
microbes
forms.
3
Vacuole
and lysosome
fuse.
4
Toxic
compounds
and lysosomal
enzymes
destroy microbes.
5
Microbial
debris is
released by
exocytosis.
6
Microbes
MACROPHAGE
Vacuole Lysosome
containing
enzymes
INTERNAL INNATE IMMUNITY
- Antimicrobial substance
 Peptides and proteins function in innate defense by
attacking microbes directly or impeding their
reproduction
 Interferon proteins provide innate defense against viruses
and help activate macrophages
 About 30 proteins make up the complement system,
which causes lysis of invading cells and helps trigger
inflammation
INTERNAL INNATE IMMUNITY
- Inflammatory response
• Inflammation can be either local or systemic (throughout the body)
• Fever is a systemic inflammatory response triggered by pyrogens released by
macrophages, and toxins from pathogens
• Septic shock is a life-threatening condition caused by an overwhelming inflammatory
response
INTERNAL INNATE IMMUNITY
Natural killer cells
 All cells in the body (except red blood cells) have a class 1
MHC protein on their surface.
 Cancerous or infected cells no longer express this protein;
natural killer (NK) cells attack these damaged cells
INTERNAL INNATE IMMUNITY
ADAPTIVE IMMUNITY
- develops after exposure to agents such as microbes,
toxins, or other foreign substances
T-Lymphocytes
 Mature T-cells have T cell receptors which have a very similar structure to
antibodies and are specific to 1 antigen.
 They are activated when the receptor comes into contact with the Ag with
another host cell (e.g. on a macrophage membrane or an invaded body
cell)
T-Lymphocytes
 After activation the cell divides to form:
 T-helper cells – secrete CYTOKINES
 help B cells divide
 stimulate macrophages
 Cytotoxic T cells (killer T cells)
 Kill body cells displaying antigen
 Memory T cells
 remain in body
Helper T cells
 Helper T-cells have receptors for recognizing antigens.
If they are presented with an antigen, they release
cytokines to stimulate B-cell division.
 The helper T-cell is the key cell to signal an immune
response. If helper T-cells are disabled, as they are in
people with AIDS, the immune system will not respond.
“Killer” T cells
 While B-cells divide and differentiate, so do T-cells.
 Some T-cells become cytotoxic, or “killer” T-cells. These T-
cells seek out and destroy any antigens in the system, and
destroy microbes “tagged” by antibodies.
 Some cytotoxic T-cells can recognize and destroy cancer cells.
B cells
 B-cells in general produce antibodies. Those with antibodies that
bind with the invader’s antigen are stimulated to reproduce rapidly.
 B-cells differentiate into either plasma cells or memory B-cells.
Plasma cells rapidly produce antibodies. Memory cells retain the
“memory” of the invader and remain ready to divide rapidly if an
invasion occurs again.
B -Lymphocytes
B -Lymphocytes
 Some activated B cells  PLASMA CELLS these produce lots of antibodies, <
1000/sec
 The antibodies travel to the blood, lymph, lining of gut and lungs.
 The number of plasma cells goes down after a few weeks
 Antibodies stay in the blood longer but eventually their numbers go down too.
B -Lymphocytes
 Some activated B cells  MEMORY CELLS.
 Memory cells divide rapidly as soon as the antigen is reintroduced.
 There are many more memory cells than there were clone cells.
 When the pathogen/infection infects again it is destroyed before any
symptoms show.
B cells recognize
antigens,
Differentiate into plasma cells-
produce more antibodies
Differentiate into memory cells-
keep some for later
proliferate,
and produce
specific
antibodies.
Antibodies
 Also known as immunoglobulins
 Globular glycoproteins
 The heavy and light chains are polypeptides
 The chains are held together by disulphide bridges
 Each ab has 2 identical ag binding sites – variable regions.
 The order of amino acids in the variable region determines
the shape of the binding site
Different Immunoglobulins
Type Number of
ag binding
sites
Site of action Functions
IgG 2 •Blood
•Tissue fluid
•CAN CROSS
PLACENTA
•Increase
macrophage activity
•Antitoxins
•Agglutination
IgM 10 •Blood
•Tissue fluid
Agglutination
IgA 2 or 4 •Secretions (saliva,
tears, small intestine,
vaginal, prostate,
nasal, breast milk)
•Stop bacteria
adhering to host
cells
•Prevents bacteria
forming colonies on
mucous membranes
IgE 2 Tissues •Activate mast cells
 HISTAMINE
•Worm response
INTERACTION OF ANTIGENS - ANTIBODIES
ANTIGEN
 a substance or molecule that is recognized by the
immune system. The molecule can be from
foreign material such as bacteria or viruses.
 Anything that can trigger this immune response is
called an antigen. An antigen can be a microbe
such as a virus, or even a part of a microbe.
Tissues or cells from another person (except an
identical twin) also carry nonself markers and act
as antigens.
ANTIGEN
Antigen-
binding
sitesAntibody A
Antigen
Antibody B
Antibody C
Epitopes
(antigenic
determinants)
 An antigen is any foreign molecule
 That is specifically recognized by lymphocytes
and elicits a response from them
 A lymphocyte actually recognizes and binds
 To just a small, accessible portion of the antigen
called an epitope
Picture Source : campbell
An antibody is a
substance formed
immunity in human
blood in response to
antigenic stimulus and
will react specifically
with antigen
Antibodies as Receptors
 Antibodies can
attach to B cells,
and serve to
recognize foreign
antigens.
Antigens as Effectors
 Free antibodies can
bind to antigens,
which “tags” the
antigen for the
immune system to
attack and destroy.
Antigen Recognition by Lymphocytes
 The vertebrate body is populated by two main types of lymphocytes
 B lymphocytes (B cells) and T lymphocytes (T cells)
 Which circulate through the blood
 The plasma membranes of both B cells
and T cells
 Have about 100,000 antigen receptor that all recognize the same epitope
Antigen-
Binding site
b chain
Disulfide bridge
a chain
T cell
A T cell receptor consists of one
a chain and one b chain linked by
a disulfide bridge.
(b)
Variable
regions
Constant
regions
Transmembrane
region
Plasma
membrane
Cytoplasm of T cell
T Cell Receptors for Antigens and the Role of the MHC
 Each T cell receptor
 Consists of two different polypeptide chains
Figure 43.8b
V V
C C
Picture Source : campbell
 T cells bind to small fragments of antigens
 That are bound to normal cell-surface proteins called
MHC molecules
 MHC molecules
 Are encoded by a family of genes called the major
histocompatibility complex
 Infected cells produce MHC molecules
 Which bind to antigen fragments and then are
transported to the cell surface in a process called
antigen presentation
 A nearby T cell
 Can then detect the antigen fragment displayed on the
cell’s surface
 Depending on their source
Peptide antigens are handled by
different classes of MHC molecules
Figure 43.9a
Infected cell
Antigen
fragment
Class I MHC
molecule
T cell
receptor
(a) Cytotoxic T cell
A fragment of
foreign protein
(antigen) inside the
cell associates with
an MHC molecule
and is transported
to the cell surface.
1
The combination of
MHC molecule and
antigen is recognized
by a T cell, alerting it
to the infection.
2
1
2
 Class I MHC molecules, found on almost all
nucleated cells of the body
 Display peptide antigens to cytotoxic T cells
Picture Source : campbell
 Class II MHC molecules, located mainly on dendritic cells, macrophages, and
B cells
 Display antigens to helper T cells
1
2
Figure 43.9b
Microbe Antigen-
presenting
cell
Antigen
fragment
Class II MHC
molecule
T cell
receptor
Helper T cell
A fragment of
foreign protein
(antigen) inside the
cell associates with
an MHC molecule
and is transported
to the cell surface.
1
The combination of
MHC molecule and
antigen is recognized
by a T cell, alerting it
to the infection.
2
(b)
Picture Source : campbell
Clonal Selection of Lymphocytes
 In a primary immune response
 Binding of antigen to a mature lymphocyte induces the
lymphocyte’s proliferation and differentiation, a
process called clonal selection
 Clonal selection of B cells
 Generates a clone of short-lived activated effector
cells and a clone of long-lived memory cells
Figure 43.12
Antigen molecules
Antigen
receptor
B cells that
differ in
antigen
specificity
Antibody
molecules
Clone of memory cells
Clone of plasma cells
Antigen molecules
bind to the antigen
receptors of only one
of the three B cells
shown.
The selected B cell
proliferates, forming
a clone of identical
cells bearing
receptors for the
selecting antigen.
Some proliferating
cells develop into
short-lived plasma
cells that secrete
antibodies specific
for the antigen.
Some proliferating cells
develop into long-lived
memory cells that can
respond rapidly upon
subsequent exposure
to the same antigen.
Picture Source : campbell
PRIMARY AND SECONDARY IMMUNE RESPONSE
Primary Immune
Response
>> In the event the primary
response stimulation, cells
divide and hold precursor
differentiation into antibody-
forming cells that produce IgM
and IgG. During the process of
memory cells are formed,
which are still limited.
Secondary Immune
Response
>> In the event secondary response,
the cells sensitive to the antigen that
number is growing rapidly increased
antibody synthesis, is faster, more
durable, and more effective than the
previous response. That is because
the immune system has been more
ready to antigens as memory cells
prepared against antigens. These
memory cells that will eventually lead
to immunological memory.
ALERGY AND ABNORMALITY OF
IMMUNE SYSTEM
Allergies
 When the immune system responds to harmless substances
 Allergens – antigenic substances which do no real harm
 Allergens include house dust, animal skin, pollen, house dust mite and its faeces
Allergies
 Histamine causes blood vessels to widen and become leaky.
 Fluid and white blood cells leave capillaries.
 The area of leakage becomes hot, red and inflamed
Smallpox
Symptoms
 Red spots containing transparent fluid all over body.
 Spots fill with pus
 Eyelids swell and become glued together
Measles
 Caused by an airborne virus
 9th leading cause of death worldwide
 Causes rash and fever
 Can have fatal complications
 Passive immunity from mothers in infants under 8 months
 Now quite a rare disease in developed countries due to vaccination
Measles
 Transmitted easily in overcrowded, insanitary conditions
 Mainly affects malnourished infants with vitamin A deficiencies
 Responsible for many cases of childhood blindness and can cause severe brain damage
 Herd immunity of 93-95% needed to prevent transmission within a population.
THANK YOU FOR YOUR ATTENTION
WASSALAMUALAIKUM WR.WB

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Sistem imun 5.

  • 1. IMMUNE SYSTEMBy : Cici Rizky Y 120210103016 Adha Qiftiyatul M 120210103020 Wulan Anggraeni 120210103048 Tesa Lusidyah 120210103052
  • 2. What is the immune system?  The body’s defense against disease causing organisms, malfunctioning cells, and foreign particles
  • 3. IMMUNE SYSTEM Adaptive Immune System (Specific respon) Innate Immune system (Non specific respon) Disorders and disease External Defense Internal Defense -Skin -Mucous membranes -secretorions -Phagocytic cells -Antimicrobial subtance -Inflammatory response -Natural killer cells Limfosit T Limfosit B
  • 4. Immune System : 2 branches 1. The Innate Immune system = - is present before any exposure to pathogens and is effective from the time of birth 2. The Adaptive Immune System = - develops after exposure to agents such as microbes, toxins, or other foreign substances
  • 5. INNATE IMMUNITY  Innate immunity is present before any exposure to pathogens and is effective from the time of birth  It involves nonspecific responses to pathogens  Innate immunity consists of external barriers plus internal cellular and chemical defenses
  • 6. Nonspecific response  Skin  Mucous membranes  Secretions EXTERNAL INNATE IMMUNITY
  • 7. - Phagocytic cells There are different types of phagocytic cells: - Neutrophils engulf and destroy microbes - Macrophages are part of the lymphatic system and are found throughout the body - Eosinophils discharge destructive enzymes - Dendritic cells stimulate development of acquired immunity Pseudopodia surround microbes. 1 Microbes are engulfed into cell. 2 Vacuole containing microbes forms. 3 Vacuole and lysosome fuse. 4 Toxic compounds and lysosomal enzymes destroy microbes. 5 Microbial debris is released by exocytosis. 6 Microbes MACROPHAGE Vacuole Lysosome containing enzymes INTERNAL INNATE IMMUNITY
  • 8. - Antimicrobial substance  Peptides and proteins function in innate defense by attacking microbes directly or impeding their reproduction  Interferon proteins provide innate defense against viruses and help activate macrophages  About 30 proteins make up the complement system, which causes lysis of invading cells and helps trigger inflammation INTERNAL INNATE IMMUNITY
  • 9. - Inflammatory response • Inflammation can be either local or systemic (throughout the body) • Fever is a systemic inflammatory response triggered by pyrogens released by macrophages, and toxins from pathogens • Septic shock is a life-threatening condition caused by an overwhelming inflammatory response INTERNAL INNATE IMMUNITY
  • 10. Natural killer cells  All cells in the body (except red blood cells) have a class 1 MHC protein on their surface.  Cancerous or infected cells no longer express this protein; natural killer (NK) cells attack these damaged cells INTERNAL INNATE IMMUNITY
  • 11. ADAPTIVE IMMUNITY - develops after exposure to agents such as microbes, toxins, or other foreign substances
  • 12. T-Lymphocytes  Mature T-cells have T cell receptors which have a very similar structure to antibodies and are specific to 1 antigen.  They are activated when the receptor comes into contact with the Ag with another host cell (e.g. on a macrophage membrane or an invaded body cell)
  • 13. T-Lymphocytes  After activation the cell divides to form:  T-helper cells – secrete CYTOKINES  help B cells divide  stimulate macrophages  Cytotoxic T cells (killer T cells)  Kill body cells displaying antigen  Memory T cells  remain in body
  • 14.
  • 15. Helper T cells  Helper T-cells have receptors for recognizing antigens. If they are presented with an antigen, they release cytokines to stimulate B-cell division.  The helper T-cell is the key cell to signal an immune response. If helper T-cells are disabled, as they are in people with AIDS, the immune system will not respond.
  • 16. “Killer” T cells  While B-cells divide and differentiate, so do T-cells.  Some T-cells become cytotoxic, or “killer” T-cells. These T- cells seek out and destroy any antigens in the system, and destroy microbes “tagged” by antibodies.  Some cytotoxic T-cells can recognize and destroy cancer cells.
  • 17. B cells  B-cells in general produce antibodies. Those with antibodies that bind with the invader’s antigen are stimulated to reproduce rapidly.  B-cells differentiate into either plasma cells or memory B-cells. Plasma cells rapidly produce antibodies. Memory cells retain the “memory” of the invader and remain ready to divide rapidly if an invasion occurs again.
  • 19. B -Lymphocytes  Some activated B cells  PLASMA CELLS these produce lots of antibodies, < 1000/sec  The antibodies travel to the blood, lymph, lining of gut and lungs.  The number of plasma cells goes down after a few weeks  Antibodies stay in the blood longer but eventually their numbers go down too.
  • 20. B -Lymphocytes  Some activated B cells  MEMORY CELLS.  Memory cells divide rapidly as soon as the antigen is reintroduced.  There are many more memory cells than there were clone cells.  When the pathogen/infection infects again it is destroyed before any symptoms show.
  • 21. B cells recognize antigens, Differentiate into plasma cells- produce more antibodies Differentiate into memory cells- keep some for later proliferate, and produce specific antibodies.
  • 22. Antibodies  Also known as immunoglobulins  Globular glycoproteins  The heavy and light chains are polypeptides  The chains are held together by disulphide bridges  Each ab has 2 identical ag binding sites – variable regions.  The order of amino acids in the variable region determines the shape of the binding site
  • 24. Type Number of ag binding sites Site of action Functions IgG 2 •Blood •Tissue fluid •CAN CROSS PLACENTA •Increase macrophage activity •Antitoxins •Agglutination IgM 10 •Blood •Tissue fluid Agglutination IgA 2 or 4 •Secretions (saliva, tears, small intestine, vaginal, prostate, nasal, breast milk) •Stop bacteria adhering to host cells •Prevents bacteria forming colonies on mucous membranes IgE 2 Tissues •Activate mast cells  HISTAMINE •Worm response
  • 25. INTERACTION OF ANTIGENS - ANTIBODIES
  • 26. ANTIGEN  a substance or molecule that is recognized by the immune system. The molecule can be from foreign material such as bacteria or viruses.  Anything that can trigger this immune response is called an antigen. An antigen can be a microbe such as a virus, or even a part of a microbe. Tissues or cells from another person (except an identical twin) also carry nonself markers and act as antigens.
  • 28. Antigen- binding sitesAntibody A Antigen Antibody B Antibody C Epitopes (antigenic determinants)  An antigen is any foreign molecule  That is specifically recognized by lymphocytes and elicits a response from them  A lymphocyte actually recognizes and binds  To just a small, accessible portion of the antigen called an epitope Picture Source : campbell An antibody is a substance formed immunity in human blood in response to antigenic stimulus and will react specifically with antigen
  • 29. Antibodies as Receptors  Antibodies can attach to B cells, and serve to recognize foreign antigens.
  • 30. Antigens as Effectors  Free antibodies can bind to antigens, which “tags” the antigen for the immune system to attack and destroy.
  • 31. Antigen Recognition by Lymphocytes  The vertebrate body is populated by two main types of lymphocytes  B lymphocytes (B cells) and T lymphocytes (T cells)  Which circulate through the blood  The plasma membranes of both B cells and T cells  Have about 100,000 antigen receptor that all recognize the same epitope
  • 32. Antigen- Binding site b chain Disulfide bridge a chain T cell A T cell receptor consists of one a chain and one b chain linked by a disulfide bridge. (b) Variable regions Constant regions Transmembrane region Plasma membrane Cytoplasm of T cell T Cell Receptors for Antigens and the Role of the MHC  Each T cell receptor  Consists of two different polypeptide chains Figure 43.8b V V C C Picture Source : campbell
  • 33.  T cells bind to small fragments of antigens  That are bound to normal cell-surface proteins called MHC molecules  MHC molecules  Are encoded by a family of genes called the major histocompatibility complex
  • 34.  Infected cells produce MHC molecules  Which bind to antigen fragments and then are transported to the cell surface in a process called antigen presentation  A nearby T cell  Can then detect the antigen fragment displayed on the cell’s surface
  • 35.  Depending on their source Peptide antigens are handled by different classes of MHC molecules
  • 36. Figure 43.9a Infected cell Antigen fragment Class I MHC molecule T cell receptor (a) Cytotoxic T cell A fragment of foreign protein (antigen) inside the cell associates with an MHC molecule and is transported to the cell surface. 1 The combination of MHC molecule and antigen is recognized by a T cell, alerting it to the infection. 2 1 2  Class I MHC molecules, found on almost all nucleated cells of the body  Display peptide antigens to cytotoxic T cells Picture Source : campbell
  • 37.  Class II MHC molecules, located mainly on dendritic cells, macrophages, and B cells  Display antigens to helper T cells 1 2 Figure 43.9b Microbe Antigen- presenting cell Antigen fragment Class II MHC molecule T cell receptor Helper T cell A fragment of foreign protein (antigen) inside the cell associates with an MHC molecule and is transported to the cell surface. 1 The combination of MHC molecule and antigen is recognized by a T cell, alerting it to the infection. 2 (b) Picture Source : campbell
  • 38. Clonal Selection of Lymphocytes  In a primary immune response  Binding of antigen to a mature lymphocyte induces the lymphocyte’s proliferation and differentiation, a process called clonal selection
  • 39.  Clonal selection of B cells  Generates a clone of short-lived activated effector cells and a clone of long-lived memory cells Figure 43.12 Antigen molecules Antigen receptor B cells that differ in antigen specificity Antibody molecules Clone of memory cells Clone of plasma cells Antigen molecules bind to the antigen receptors of only one of the three B cells shown. The selected B cell proliferates, forming a clone of identical cells bearing receptors for the selecting antigen. Some proliferating cells develop into short-lived plasma cells that secrete antibodies specific for the antigen. Some proliferating cells develop into long-lived memory cells that can respond rapidly upon subsequent exposure to the same antigen. Picture Source : campbell
  • 40.
  • 41. PRIMARY AND SECONDARY IMMUNE RESPONSE
  • 42. Primary Immune Response >> In the event the primary response stimulation, cells divide and hold precursor differentiation into antibody- forming cells that produce IgM and IgG. During the process of memory cells are formed, which are still limited. Secondary Immune Response >> In the event secondary response, the cells sensitive to the antigen that number is growing rapidly increased antibody synthesis, is faster, more durable, and more effective than the previous response. That is because the immune system has been more ready to antigens as memory cells prepared against antigens. These memory cells that will eventually lead to immunological memory.
  • 43.
  • 44. ALERGY AND ABNORMALITY OF IMMUNE SYSTEM
  • 45. Allergies  When the immune system responds to harmless substances  Allergens – antigenic substances which do no real harm  Allergens include house dust, animal skin, pollen, house dust mite and its faeces
  • 46.
  • 47. Allergies  Histamine causes blood vessels to widen and become leaky.  Fluid and white blood cells leave capillaries.  The area of leakage becomes hot, red and inflamed
  • 48.
  • 49. Smallpox Symptoms  Red spots containing transparent fluid all over body.  Spots fill with pus  Eyelids swell and become glued together
  • 50. Measles  Caused by an airborne virus  9th leading cause of death worldwide  Causes rash and fever  Can have fatal complications  Passive immunity from mothers in infants under 8 months  Now quite a rare disease in developed countries due to vaccination
  • 51. Measles  Transmitted easily in overcrowded, insanitary conditions  Mainly affects malnourished infants with vitamin A deficiencies  Responsible for many cases of childhood blindness and can cause severe brain damage  Herd immunity of 93-95% needed to prevent transmission within a population.
  • 52. THANK YOU FOR YOUR ATTENTION WASSALAMUALAIKUM WR.WB