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IMMUNOLOGY
Immunity is body's ability to resist or eliminate
potentially harmful foreign materials or
abnormal cells.
• IMMUNITY
• Derived from ‘immunis’- Latin-exempt,
state of protection from infectious
diseases).
• The term immunity refers to the resistance
exhibited by the host towards infections
caused by microorganisms and their
products (toxins).
THE MAIN FUNCTIONS OF
IMMUNE SYSTEM – 4 Rs
Recognize pathogen
Respond to it
Remove it
Remember it
Healthy immunity accomplishes FOUR essential principles:
(1) ability to detect and fight off infection;
(2) ability to recognize a host's own cells as "self," thereby
protecting them from attack;
(3) a memory from previous foreign infections; and
(4) ability to limit the response after the pathogen has been
removed.
• CONSISTS OF FOLLOWING ACTIVITIES:
• Defense against invading pathogens (viruses & bacteria)
• Removal of 'worn-out' cells (e.g., old RBCs) & tissue debris
(e.g., from injury or disease)
• Identification & destruction of abnormal or mutant cells
(primary defense against cancer)
• Rejection of 'foreign' cells (e.g., organ transplant)
• Inappropriate responses:
• Allergies - response to normally harmless substances
Autoimmune diseases
DEFINITIONS
 Immunity = resistance of a host to pathogens and their toxic effects
 Immune system = cells, tissues, and organs that mediate resistance
to infections
 Immune response = collective and coordinated response to the
introduction of foreign substances in an individual mediated by the
cells and molecules of the immune system
 Immunology = study of structure and function of the immune
system
IMMUNE SYSTEM
ORGANS CELLS MOLECULES
Bone marrow
Thymus
Spleen
Lymph nodes
Payer’s patches
Tonsils and adenoids
Appendix
Lymphatic vessels
Lymphocytes
B-Lymphocytes, plasma cells
T-lymphocytes
natural killer lymphocytes
Monocytes, Macrophage
Granulocytes
neutrophils
eosinophils
Basophils
Antibodies
Complement
Cytokines
Interleukins
Interferons
OVERVIEW OF IMMUNE SYSTEN
Immunity
Innate
(Nonspecific)
1o line of
defense
Acquired
(Specific)
2o line of
defense
DEFINITIONS
Innate immunity is natural immunity and
inherited along with birth. Eg. Sweat and
tears.
 Acquired immunity is obtained during one’s
life time. It is an adaptation against previous
infection. Eg. Resistance developed after
measles or mumps.
THE INNATE IMMUNE SYSTEM
Innate immunity (also called nonspecific or natural immunity)
refers to the inborn-ability of the body to resist, and is genetically
transmitted from one generation to the next. This immunity offers
resistance to any microorganism or foreign material encountered
by the host.
It includes general mechanisms inherited as part of the innate
structure and function of each vertebrate, and acts as first line of
defence. Innate immunity lacks immunological memory, i.e., it
occurs to the same extent each time a microorganism or foreign
material is encountered.
FEATURES OF INNATE IMMUNITY
 Acts as first line of defense
 Based on genetic make-up
 Relies on already formed components
 Rapid response: within minutes of infection
 Not specific
 same molecules / cells respond to a range of pathogens
 Has no memory
 same response after repeated exposure
 Does not lead to clonal expansion
Mechanism of innate immunity:
1. Anatomical / mechanical / physical barrier
2. Physiological / biochemical barrier
3. Cellular factors / Phagocytic barrier
4. Inflammatory barrier / Inflammation
I. ANATOMICAL BARRIERS – PHYSICAL /
MECHANICAL FACTORS
1. Skin 2. mucociliary escalator
3. Flushing action of
saliva, tears and urine
sneezing coughing
vomitting
I. ANATOMICAL BARRIERS
1.SKIN- horny outer layer-stratum corneum-impermeable to infectious
microbes. Microbes enter through skin only when skin is damaged.
2.Mucous membrane- line respiratory, gastrointestinal, urogenital
passage prevent the adherence of bacteria to the epithelial cells.
mucus coated nose hairs trap microbes; mucus coated dust or
microbes pushed outward either by sneezing or coughing (speed up
process).
3. cilia- lined respiratory passage-sweep away the mucus trapped
microbes in this passage by their constant movement.
I. ANATOMICAL BARRIERS
4. Peristalsis- by constant peristaltic movement the pathogens in the
intestine are pushed away before they could invade and grow there-
vomiting in response to microbial toxins.
5. Tears-lacrimal secretion of the eye -constantly wash over the eye to
flush away the foreign particles.
6. Saliva- constantly washes over teeth and mouth and the pathogens
if any swallowed by the mouth along with salivary secretion.
7. Urine- flushing mechanism prevents colonization of microbes in the
urinary tract.
II. Physiological / Biochemical factors
1. Secretion of the skin
2. Secretion of the digestive tract
3. Human milk
4. Nasal secretion and Saliva
5. Lysozyme
6. Interferons
7. Complement
8. Properdin
9. Secretion of bacterial flora
10. Semen
11. Acute phase proteins
III. Cellular factors
Natural immunity is provided by 2 cellular factors;
 1. Phagocytosis – phago –eating; cyto- cell
 2. Natural Killer cells (NK cells- non phagocytic)
III. Cellular factors
III. Cellular factors
 Metchinikoff (1838)- microphage and
 macrophage (big eaters)
 -PMN cells are microphages- neutrophils (in blood),
eosinophils and basophils.
 MN cells- monocytes- macrophages
phagocytosis of microbes (in tissues)-
presentation
III. Cellular factors
2. Natural Killer Cells
-non phagocytic with large granules
-originate from lymphoid progenitor along with T and B
cells
-show natural cytotoxicity and they themselves identify a
range of tumour cells and cells infected with viruses
without any antigenic stimulation. So, they named NK cells
NK cells choose cells to kill
Some surface proteins are missing
Toll-like receptors (TLRs)
• Transmembrane proteins
• Present on macrophages / few other cells
• Conserved across vertebrates
• Important part of innate immune system
Toll-like receptors (TLRs)
They look out for microbes (or their components) Bind with microbes or their components
What happens when TLR bind to a microbe
TLR binding
to microbe
inflammation
Phagocytosis of
infected cell
Secretion of cytokines/
INF
Apoptosis of
infected cell
Cytokines
 Small proteins – secreted by cells of
the immune system
 Affect the behaviour of other cells
 signalling molecules
 Key players in innate and
acquired immunity
Which cells release cytokines ?
 Neutrophils – when they encounter a pathogen
 Macrophages – when they encounter a pathogen
 TLRs – bind to microbe / components of a microbe
 NK cells – on encountering a microbe infected cell /tumour cell
 Lymphocytes – when they are activated
Examples of cytokines
 Interferons
 Interleukins
 Tumour necrosis factor (TNF)
Interferons (IFN)
 Signalling proteins produced by virus infected monocytes and
lymphocytes
 Secreted proteins – Key anti-viral proteins
 “Interfere” with virus replication
 Warn the neighbouring cells that a virus is around...
 If we did not have IFNs – most of us may die of influenza virus infection
How does IFN warn the neighbouring cells ?
The infected cells release IFN
Antiviral state
Antiviral state
Antiviral state
Antiviral state
Virus infects the neighbouring cells
Antiviral state
Antiviral state
Antiviral state
Prewarned cells are able to quickly inhibit
the virus
Interleukins
 Interleukins – 1-37
 Not stored inside cells
 Quickly synthesized and secreted in response to infection
 Key modulators of behaviour of immune cells
 Mostly secreted by T-lymphocytes & macrophages
What to interleukins do ?
Tumour necrosis factor (TNF)
IV. INFLAMMATION
 Complex biological process by which body
responds to pathogens and irritants
 Associated with swelling of tissue
 Key player in innate immune response
Signs of inflammation
SIGNS OF INFLAMMATION
INFLAMMATION AND INNATE IMMUNITY
Mast cells – similar to basophils in blood;
mast cells are present in tissues and release histamines in response to wound / infection /irritant
FEVER
 Inflammatory response is often accompanied by fever.
 Some cytokines stimulate the brain to make
prostaglandins. These prostaglandins stimulate the
hypothalamus to a new temperature set point. The signals
the hypothalamus sends out then:
 Constrict blood vessels in the skin
 Contract skeletal muscles
 Increase heart rate and respiration
OTHER FACTORS OR TYPES OF INNATE IMMUNITY
 1. GENETIC FACTORS- Innate immunity is mainly due to
genetic factors thereby differs at the level of species,
races and individuals.
Species immunity
Resistance to a pathogen exhibited by all
members of a species.
Eg: Human beings are highly susceptible to
common cold but not dogs.
Rats are insusceptible to diphtheria but humans
are susceptible
Racial immunity
 Within a species, different races may show
differences in susceptibility to infections
 Eg: In U.S.A. Negroes are more susceptible to TB
than whites
Individual immunity
 The differences in innate immunity shown
by different individuals of the same race .
 Eg: identical twins exhibit similar degrees
of resistance or susceptibility to leprosy
and tuberculosis but not the heterozygous
twins.
2. Body temperature
 Body temperature is also very important in determining innate
immunity.
 Eg: cold blooded animals are not infected with tubercle bacilli
but pathogenic to mammals (warm blooded)
 Hens are naturally immune to anthrax because of its body
temp. of 40°.
 Gonococci are readily killed at the temp. over 40. so, in this
case fever therapy was used earlier before the penicillin .
3. Fever
 A rise in temp. (pyrexia) after
infection is a natural defence
mechanism.
 Accelerates the physiological
processes
 May destroy infectious
pathogens in some cases
 Stimulates the production of INF
and helps to recover from virus
infections
THE ACQUIRED IMMUNE SYSTEM
 Acquired immunity is obtained during life time.
 It is an adaptation against previous infection.
 Actually it forms third line of defence
 It is caused by specific antigens
Acquired immunity
Active Acquired Immunity
Developed as a result of natural infection or vaccination
Involves the synthesis of specific antibodies or production of
immunologically active cells
When the antigen enters the body for the first time, it produces an
immune response called primary immune response. It can produce
memory cells.
When the same antigen enters for the second time it produces
secondary immune response.
Natural Active Immunity
Why common cold does not provide us immunity
Types of Immunology
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Food safety_Challenges food safety laboratories_.pdf
 

Types of Immunology

  • 2. Immunity is body's ability to resist or eliminate potentially harmful foreign materials or abnormal cells.
  • 3. • IMMUNITY • Derived from ‘immunis’- Latin-exempt, state of protection from infectious diseases). • The term immunity refers to the resistance exhibited by the host towards infections caused by microorganisms and their products (toxins).
  • 4. THE MAIN FUNCTIONS OF IMMUNE SYSTEM – 4 Rs Recognize pathogen Respond to it Remove it Remember it
  • 5. Healthy immunity accomplishes FOUR essential principles: (1) ability to detect and fight off infection; (2) ability to recognize a host's own cells as "self," thereby protecting them from attack; (3) a memory from previous foreign infections; and (4) ability to limit the response after the pathogen has been removed.
  • 6. • CONSISTS OF FOLLOWING ACTIVITIES: • Defense against invading pathogens (viruses & bacteria) • Removal of 'worn-out' cells (e.g., old RBCs) & tissue debris (e.g., from injury or disease) • Identification & destruction of abnormal or mutant cells (primary defense against cancer) • Rejection of 'foreign' cells (e.g., organ transplant) • Inappropriate responses: • Allergies - response to normally harmless substances Autoimmune diseases
  • 7. DEFINITIONS  Immunity = resistance of a host to pathogens and their toxic effects  Immune system = cells, tissues, and organs that mediate resistance to infections  Immune response = collective and coordinated response to the introduction of foreign substances in an individual mediated by the cells and molecules of the immune system  Immunology = study of structure and function of the immune system
  • 8. IMMUNE SYSTEM ORGANS CELLS MOLECULES Bone marrow Thymus Spleen Lymph nodes Payer’s patches Tonsils and adenoids Appendix Lymphatic vessels Lymphocytes B-Lymphocytes, plasma cells T-lymphocytes natural killer lymphocytes Monocytes, Macrophage Granulocytes neutrophils eosinophils Basophils Antibodies Complement Cytokines Interleukins Interferons
  • 9. OVERVIEW OF IMMUNE SYSTEN Immunity Innate (Nonspecific) 1o line of defense Acquired (Specific) 2o line of defense
  • 10. DEFINITIONS Innate immunity is natural immunity and inherited along with birth. Eg. Sweat and tears.  Acquired immunity is obtained during one’s life time. It is an adaptation against previous infection. Eg. Resistance developed after measles or mumps.
  • 11. THE INNATE IMMUNE SYSTEM Innate immunity (also called nonspecific or natural immunity) refers to the inborn-ability of the body to resist, and is genetically transmitted from one generation to the next. This immunity offers resistance to any microorganism or foreign material encountered by the host. It includes general mechanisms inherited as part of the innate structure and function of each vertebrate, and acts as first line of defence. Innate immunity lacks immunological memory, i.e., it occurs to the same extent each time a microorganism or foreign material is encountered.
  • 12. FEATURES OF INNATE IMMUNITY  Acts as first line of defense  Based on genetic make-up  Relies on already formed components  Rapid response: within minutes of infection  Not specific  same molecules / cells respond to a range of pathogens  Has no memory  same response after repeated exposure  Does not lead to clonal expansion
  • 13. Mechanism of innate immunity: 1. Anatomical / mechanical / physical barrier 2. Physiological / biochemical barrier 3. Cellular factors / Phagocytic barrier 4. Inflammatory barrier / Inflammation
  • 14. I. ANATOMICAL BARRIERS – PHYSICAL / MECHANICAL FACTORS 1. Skin 2. mucociliary escalator 3. Flushing action of saliva, tears and urine sneezing coughing vomitting
  • 15. I. ANATOMICAL BARRIERS 1.SKIN- horny outer layer-stratum corneum-impermeable to infectious microbes. Microbes enter through skin only when skin is damaged. 2.Mucous membrane- line respiratory, gastrointestinal, urogenital passage prevent the adherence of bacteria to the epithelial cells. mucus coated nose hairs trap microbes; mucus coated dust or microbes pushed outward either by sneezing or coughing (speed up process). 3. cilia- lined respiratory passage-sweep away the mucus trapped microbes in this passage by their constant movement.
  • 16. I. ANATOMICAL BARRIERS 4. Peristalsis- by constant peristaltic movement the pathogens in the intestine are pushed away before they could invade and grow there- vomiting in response to microbial toxins. 5. Tears-lacrimal secretion of the eye -constantly wash over the eye to flush away the foreign particles. 6. Saliva- constantly washes over teeth and mouth and the pathogens if any swallowed by the mouth along with salivary secretion. 7. Urine- flushing mechanism prevents colonization of microbes in the urinary tract.
  • 17. II. Physiological / Biochemical factors 1. Secretion of the skin 2. Secretion of the digestive tract 3. Human milk 4. Nasal secretion and Saliva 5. Lysozyme 6. Interferons 7. Complement 8. Properdin 9. Secretion of bacterial flora 10. Semen 11. Acute phase proteins
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  • 19. III. Cellular factors Natural immunity is provided by 2 cellular factors;  1. Phagocytosis – phago –eating; cyto- cell  2. Natural Killer cells (NK cells- non phagocytic)
  • 21. III. Cellular factors  Metchinikoff (1838)- microphage and  macrophage (big eaters)  -PMN cells are microphages- neutrophils (in blood), eosinophils and basophils.  MN cells- monocytes- macrophages phagocytosis of microbes (in tissues)- presentation
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  • 23. III. Cellular factors 2. Natural Killer Cells -non phagocytic with large granules -originate from lymphoid progenitor along with T and B cells -show natural cytotoxicity and they themselves identify a range of tumour cells and cells infected with viruses without any antigenic stimulation. So, they named NK cells
  • 24. NK cells choose cells to kill Some surface proteins are missing
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  • 26. Toll-like receptors (TLRs) • Transmembrane proteins • Present on macrophages / few other cells • Conserved across vertebrates • Important part of innate immune system
  • 27. Toll-like receptors (TLRs) They look out for microbes (or their components) Bind with microbes or their components
  • 28. What happens when TLR bind to a microbe TLR binding to microbe inflammation Phagocytosis of infected cell Secretion of cytokines/ INF Apoptosis of infected cell
  • 29. Cytokines  Small proteins – secreted by cells of the immune system  Affect the behaviour of other cells  signalling molecules  Key players in innate and acquired immunity
  • 30. Which cells release cytokines ?  Neutrophils – when they encounter a pathogen  Macrophages – when they encounter a pathogen  TLRs – bind to microbe / components of a microbe  NK cells – on encountering a microbe infected cell /tumour cell  Lymphocytes – when they are activated
  • 31. Examples of cytokines  Interferons  Interleukins  Tumour necrosis factor (TNF)
  • 32. Interferons (IFN)  Signalling proteins produced by virus infected monocytes and lymphocytes  Secreted proteins – Key anti-viral proteins  “Interfere” with virus replication  Warn the neighbouring cells that a virus is around...  If we did not have IFNs – most of us may die of influenza virus infection
  • 33. How does IFN warn the neighbouring cells ?
  • 34. The infected cells release IFN Antiviral state Antiviral state Antiviral state Antiviral state
  • 35. Virus infects the neighbouring cells Antiviral state Antiviral state Antiviral state
  • 36. Prewarned cells are able to quickly inhibit the virus
  • 37. Interleukins  Interleukins – 1-37  Not stored inside cells  Quickly synthesized and secreted in response to infection  Key modulators of behaviour of immune cells  Mostly secreted by T-lymphocytes & macrophages
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  • 44. IV. INFLAMMATION  Complex biological process by which body responds to pathogens and irritants  Associated with swelling of tissue  Key player in innate immune response
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  • 48. INFLAMMATION AND INNATE IMMUNITY Mast cells – similar to basophils in blood; mast cells are present in tissues and release histamines in response to wound / infection /irritant
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  • 50. FEVER  Inflammatory response is often accompanied by fever.  Some cytokines stimulate the brain to make prostaglandins. These prostaglandins stimulate the hypothalamus to a new temperature set point. The signals the hypothalamus sends out then:  Constrict blood vessels in the skin  Contract skeletal muscles  Increase heart rate and respiration
  • 51. OTHER FACTORS OR TYPES OF INNATE IMMUNITY  1. GENETIC FACTORS- Innate immunity is mainly due to genetic factors thereby differs at the level of species, races and individuals.
  • 52. Species immunity Resistance to a pathogen exhibited by all members of a species. Eg: Human beings are highly susceptible to common cold but not dogs. Rats are insusceptible to diphtheria but humans are susceptible
  • 53. Racial immunity  Within a species, different races may show differences in susceptibility to infections  Eg: In U.S.A. Negroes are more susceptible to TB than whites
  • 54. Individual immunity  The differences in innate immunity shown by different individuals of the same race .  Eg: identical twins exhibit similar degrees of resistance or susceptibility to leprosy and tuberculosis but not the heterozygous twins.
  • 55. 2. Body temperature  Body temperature is also very important in determining innate immunity.  Eg: cold blooded animals are not infected with tubercle bacilli but pathogenic to mammals (warm blooded)  Hens are naturally immune to anthrax because of its body temp. of 40°.  Gonococci are readily killed at the temp. over 40. so, in this case fever therapy was used earlier before the penicillin .
  • 56. 3. Fever  A rise in temp. (pyrexia) after infection is a natural defence mechanism.  Accelerates the physiological processes  May destroy infectious pathogens in some cases  Stimulates the production of INF and helps to recover from virus infections
  • 57. THE ACQUIRED IMMUNE SYSTEM  Acquired immunity is obtained during life time.  It is an adaptation against previous infection.  Actually it forms third line of defence  It is caused by specific antigens
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  • 64. Active Acquired Immunity Developed as a result of natural infection or vaccination Involves the synthesis of specific antibodies or production of immunologically active cells When the antigen enters the body for the first time, it produces an immune response called primary immune response. It can produce memory cells. When the same antigen enters for the second time it produces secondary immune response.
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  • 66. Natural Active Immunity Why common cold does not provide us immunity