05/30/11 22:58
05/30/11 22:58
Understandin
g Immunology
Dr. Ahmed Elshebiny , MD
Dr. Ahmed Elshebiny , MD
Lecturer of Internal Medicine
Lecturer of Internal Medicine
Faculty of Medicine, Menoufyia University
Faculty of Medicine, Menoufyia University
Former Clinical Research Fellow,
Former Clinical Research Fellow,
Joslin Diabetes Center, Harvard University
Joslin Diabetes Center, Harvard University
05/30/11 22:58
Immunology Course
 Basics:
Immune system and disease
 Diseases:
Immunopatholy
 Applications:
Therapeutic applications
05/30/11 22:58
Immune system and disease
 Immunity
 Immune system
 Innate Immunity
 Adaptive Immunity
 Immune Recognition
 Cells of the Immune system
 Complement
 Immunoglobulins
 Cytokines
 Human disease & Immunity
 Immunopathology
 Diagnostics
 Therapeutic applications
Structure and
Function of The
System
Cells and
Molecules of
Immunity
Introduction to
Clinical
Immunology
05/30/11 22:58
Immunity
05/30/11 22:58
Immunity is characterized by:
 Specificity – activated by and responds to a
specific antigen
 Versatility – is ready to confront any antigen
at any time
 Memory – “remembers” any antigen it has
encountered
 Tolerance – responds to foreign substances
but ignores normal tissues
05/30/11 22:58
History of discovery of immunity
 “Immune” meaning
 Noticing immunity centuries ago
 Small pox
 Edward Jenner
 Recent developments
05/30/11 22:58
05/30/11 22:58
1st
Line defense:
Physical and chemical barriers
 Skin – acts as a barrier to invasion
 Sweat – has chemicals which can kill different
pathogens.
 Tears - have lysozyme which has powerful digestive
abilities that render antigens harmless.
 Saliva – also has lysozyme.
 Mucus - can trap pathogens, which are then sneezed,
coughed, washed away, or destroyed by chemicals.
 Stomach Acid – destroys pathogens
05/30/11 22:58
Innate Adaptive
Immunity
Cellular Humoral
Cellular Humoral
Let us see this video about immunity
05/30/11 22:58
Inflammation
Inflammation is a
nonspecific
response of living
tissue to localize
and eliminate the
injurious agent
Immune Response
05/30/11 22:58
Inflammation
 The word inflammation means "setting on
fire" (16th century), and the process has been
known since ancient Egyptian times (c. 2500
B.C)
 The cardinal signs of redness, swelling,
heat, and pain were described by Celsus
(first-century A.D.), and loss of function was
added by Galen (130-200 A.D)
05/30/11 22:58
Acute phase changes
 characterized by pronounced behavioral,
physiologic, biochemical and nutritional
changes
 Acute phase reactants
 Acute phase proteins
05/30/11 22:58
C-reactive protein
 named for its capacity to precipitate the
somatic C-polysaccharide of Streptococcus
Pneumoniae.
 Systemic marker of inflammation
 produced by hepatocytes, predominantly
under transcriptional control by the cytokine
IL-6
05/30/11 22:58
The Immune system
 The immune system
recognizes, attacks,
destroys, and
remembers each
pathogen that enters
the body.
 It does this by
making specialized
cells
and antibodies that
render the
pathogens harmless.
05/30/11 22:58
05/30/11 22:58
Questions ?
 What Happens during an infection ?
 How can immune cells distinguish foreign
invaders from our own cells ?
 How can we make 100,000,000 different
antibodies with only 30,000 genes ?
05/30/11 22:58
Cells of the immune system
T-cell development
05/30/11 22:58
Cells of the immune system
05/30/11 22:58
Polymorphonuclear cells
1- Neutrophils
 Stored in bone marrow
 Released in response to infection
 Have surface receptors for IgG,
IgA, complement
 Phagocytose and destroy bacteria
 Short lived
 Dead neutrophils make a part of
pus
05/30/11 22:58
Polymorphonuclear cells
2-Basophils and mast cells
 Basophil circulate
 Mast cells are tissue bound
 Released in response to infection
 Have surface receptors for IgE, complement C3, C5
 Produce histamine, prostaglandins, leukotrienes and
proteases
 Involved in immune response to parasites
 Involved in immediate hypersensitivity
05/30/11 22:58
Polymorphonuclear cells
3-Eosinophils
 Allergy
 Have surface receptors for IgG, complement
C3, C5
 Also binds to IgE but less than mast cells or
basophils
 Phagocytose antigen antibody complexes
05/30/11 22:58
Macrophage
 In the tissues
 Long lived
 Initiate immune responses as they display antigens
from the pathogens to the lymphocytes.
05/30/11 22:58
Phagocytosis
05/30/11 22:58
Lymphocytes
 B and T cells mature then
circulate in the blood and
lymph
 B-cells mature in bone
marrow
 T-cells mature in thymus
05/30/11 22:58
B-Lymphocytes
 The huge variety is caused
by genes coding for abs
changing slightly during
development.
 The number of plasma cells
goes down after a few
weeks
 Antibodies stay in the
blood longer but eventually
their numbers go down too.
05/30/11 22:58
T-Lymphocytes
 CD3 in all types
 CD4 in helper
 CD8 in cytotoxic
05/30/11 22:58
05/30/11 22:58
Natural killer cells
 Large granular lymphocytes
 Recognize and destroy cells bedaring viral or
tumor surface markers
05/30/11 22:58
Complement
Definition : series of heat-labile serum proteins
Site : serum and all tissue fluids except urine and CSF
Synthesis : in liver – appear in fetal circulation during 1st
13 W
Function : Responsible for certain aspects of
immune response and inflammatory response
Activation : antigen-antibody complex or endotoxin, capsule
series of proteins activated sequentially
Inactivation: inhibitors in plasma (short lived)
05/30/11 22:58
Complement system
 Plasma protein sequence cascade
 Triggered by
 Classic pathway
 Alternative pathway
 Lectin binding
Complement
05/30/11
05/30/11 22:58
22:58
Complement Activation
Complement Activation
Classical Pathway
Classical Pathway C
C1
1
C
C4
4 C
C2
2
C
C3
3 Alternative pathway
Alternative pathway
C
C5
5
C
C6
6
C
C7
7
C
C8
8
C
C9
9
Membrane damage
Membrane damage
05/30/11
05/30/11 22:58
22:58
Classic And Alterenative pathways
Classic And Alterenative pathways
Classic Pathway Alternative pathway
Classic Pathway Alternative pathway
* Specific acquired immunity * Non-specific innate immunity
* Specific acquired immunity * Non-specific innate immunity
* Initiated by antibody * Bacterial endotoxin, capsule
* Initiated by antibody * Bacterial endotoxin, capsule
* Interaction of all components * C1, C4, C2 are by-passed
* Interaction of all components * C1, C4, C2 are by-passed
* Properdin system not involved * Properdin system is involved
* Properdin system not involved * Properdin system is involved
05/30/11 22:58
Complement and disease
 Complement difficiency
 Difficiency of classic pathway components
 C3 difficiency
 Terminal complement protein difficiencies
 Difficiency of regulatory proteins
 Heriditary angioedema
 PNH
 Complement consumption as in SLE
05/30/11 22:58
Functions of Complement
 Biologically active complement products
have 3 main functions
 Opsonisation …… C3b
 Chemotaxis and inflammation……C3a, C5a
 Cell lysis……….. C5,C6,C7,C8,C9
05/30/11 22:58
Immunoglobulins
05/30/11 22:58
05/30/11 22:58
Immunoglobulins & age
05/30/11 22:58
Plasma protein electrophoresis
05/30/11 22:58
Antigens
 Antigens are macromolecules that elicit an immune
response in the body. The most common antigens
are proteins and polysaccharides.
 Hapten: incomplete Ag which can be conjugated
with a carrier protein to form a complete Ag.
05/30/11 22:58
Cytokines
 hormone-like soluble low molecular weight
protein molecules that act, generally in a
paracrine fashion, to regulate immune
responses
 They are secreted not only by lymphocytes
and macrophages but also by endothelial
cells, adipocytes, neurons, glial cells, and
other types of cells
05/30/11 22:58
Chemokines
 cytokines that regulate cell movement and
trafficking; they attract neutrophils and other
white blood cells to areas of inflammation or
immune response.
05/30/11 22:58
Interferons
 are potent cytokines that possess antiviral,
immunomodulating, and antiproliferative activities
 Interferon-α, Interferon-β & Interferon-γ
 Recombinant, natural, and pegylated IFNs currently
are available for treatment of
 condyloma acuminatum, chronic HCV infection, chronic
HBV infection,
 Kaposi's sarcoma in HIV-infected patients,
 other malignancies,
 multiple sclerosis
05/30/11 22:58
Tolerance
 It is a specific immunologic unresponsiveness
 Unresponsiveness to self antigens is known as
auto tolerance
05/30/11 22:58
Tolerance
B-cells become tolerant to self by two mechanisms:
1) Clonal deletion
Probably while B-cell precursors are in bon marrow
2) Clonal anergy
B cells in the periphery
 Tolerance in B-cells is less complete than in T-cells
 The most autoimmune diseases are mediated by antibodies
05/30/11 22:58
Factors affecting induction of tolerance
 Maturity of the immune system
 Antigen complexity
 Antigen dose
 Continuous presence of antigen
 Immunosuppressive drugs
05/30/11 22:58
Clinical importance of tolerance
 Organ transplantation
 Tumor development
 Autoimmune diseases
05/30/11 22:58
Autoimmune Diseases
 Autoimmune diseases occur due to breakdown of
the mechanisms that maintain auto tolerance
 Auto-antibodies and self reactive T-cells are
produced, resulting in tissue damage by several
mechanisms
05/30/11 22:58
References
 Lecture notes: Immunology 2010
 Essential revision notes for MRCP 2009
 Merck manual : online textbook
 Kumar & Klark : Clinical Medicine 2009
 Other Web Resources & books
05/30/11 22:58
05/30/11 22:58
Understandin
g
Immunology(2
)
05/30/11 22:58
Immunodeficiency
Immunopathology
Autoimmunity
Hypersensitivity
Lymphoproliferative
Diseases
05/30/11 22:58
References
 Lecture notes: Immunology 2010
 Essential revision notes for MRCP 2009
 Merck manual : online textbook
 Kumar & Klark : Clinical Medicine 2009
 Other Web Resources & books
05/30/11 22:58
05/30/11 22:58
Understandin
g Immunology
(3)
05/30/11 22:58
References
 Lecture notes: Immunology 2010
 Essential revision notes for MRCP 2009
 Merck manual : online textbook
 Kumar & Klark : Clinical Medicine 2009
 Other Web Resources & books
05/30/11 22:58

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Understanding immunology for internists

  • 2. 05/30/11 22:58 Understandin g Immunology Dr. Ahmed Elshebiny , MD Dr. Ahmed Elshebiny , MD Lecturer of Internal Medicine Lecturer of Internal Medicine Faculty of Medicine, Menoufyia University Faculty of Medicine, Menoufyia University Former Clinical Research Fellow, Former Clinical Research Fellow, Joslin Diabetes Center, Harvard University Joslin Diabetes Center, Harvard University
  • 3. 05/30/11 22:58 Immunology Course  Basics: Immune system and disease  Diseases: Immunopatholy  Applications: Therapeutic applications
  • 4. 05/30/11 22:58 Immune system and disease  Immunity  Immune system  Innate Immunity  Adaptive Immunity  Immune Recognition  Cells of the Immune system  Complement  Immunoglobulins  Cytokines  Human disease & Immunity  Immunopathology  Diagnostics  Therapeutic applications Structure and Function of The System Cells and Molecules of Immunity Introduction to Clinical Immunology
  • 6. 05/30/11 22:58 Immunity is characterized by:  Specificity – activated by and responds to a specific antigen  Versatility – is ready to confront any antigen at any time  Memory – “remembers” any antigen it has encountered  Tolerance – responds to foreign substances but ignores normal tissues
  • 7. 05/30/11 22:58 History of discovery of immunity  “Immune” meaning  Noticing immunity centuries ago  Small pox  Edward Jenner  Recent developments
  • 9. 05/30/11 22:58 1st Line defense: Physical and chemical barriers  Skin – acts as a barrier to invasion  Sweat – has chemicals which can kill different pathogens.  Tears - have lysozyme which has powerful digestive abilities that render antigens harmless.  Saliva – also has lysozyme.  Mucus - can trap pathogens, which are then sneezed, coughed, washed away, or destroyed by chemicals.  Stomach Acid – destroys pathogens
  • 10. 05/30/11 22:58 Innate Adaptive Immunity Cellular Humoral Cellular Humoral Let us see this video about immunity
  • 11. 05/30/11 22:58 Inflammation Inflammation is a nonspecific response of living tissue to localize and eliminate the injurious agent Immune Response
  • 12. 05/30/11 22:58 Inflammation  The word inflammation means "setting on fire" (16th century), and the process has been known since ancient Egyptian times (c. 2500 B.C)  The cardinal signs of redness, swelling, heat, and pain were described by Celsus (first-century A.D.), and loss of function was added by Galen (130-200 A.D)
  • 13. 05/30/11 22:58 Acute phase changes  characterized by pronounced behavioral, physiologic, biochemical and nutritional changes  Acute phase reactants  Acute phase proteins
  • 14. 05/30/11 22:58 C-reactive protein  named for its capacity to precipitate the somatic C-polysaccharide of Streptococcus Pneumoniae.  Systemic marker of inflammation  produced by hepatocytes, predominantly under transcriptional control by the cytokine IL-6
  • 15. 05/30/11 22:58 The Immune system  The immune system recognizes, attacks, destroys, and remembers each pathogen that enters the body.  It does this by making specialized cells and antibodies that render the pathogens harmless.
  • 17. 05/30/11 22:58 Questions ?  What Happens during an infection ?  How can immune cells distinguish foreign invaders from our own cells ?  How can we make 100,000,000 different antibodies with only 30,000 genes ?
  • 18. 05/30/11 22:58 Cells of the immune system T-cell development
  • 19. 05/30/11 22:58 Cells of the immune system
  • 20. 05/30/11 22:58 Polymorphonuclear cells 1- Neutrophils  Stored in bone marrow  Released in response to infection  Have surface receptors for IgG, IgA, complement  Phagocytose and destroy bacteria  Short lived  Dead neutrophils make a part of pus
  • 21. 05/30/11 22:58 Polymorphonuclear cells 2-Basophils and mast cells  Basophil circulate  Mast cells are tissue bound  Released in response to infection  Have surface receptors for IgE, complement C3, C5  Produce histamine, prostaglandins, leukotrienes and proteases  Involved in immune response to parasites  Involved in immediate hypersensitivity
  • 22. 05/30/11 22:58 Polymorphonuclear cells 3-Eosinophils  Allergy  Have surface receptors for IgG, complement C3, C5  Also binds to IgE but less than mast cells or basophils  Phagocytose antigen antibody complexes
  • 23. 05/30/11 22:58 Macrophage  In the tissues  Long lived  Initiate immune responses as they display antigens from the pathogens to the lymphocytes.
  • 25. 05/30/11 22:58 Lymphocytes  B and T cells mature then circulate in the blood and lymph  B-cells mature in bone marrow  T-cells mature in thymus
  • 26. 05/30/11 22:58 B-Lymphocytes  The huge variety is caused by genes coding for abs changing slightly during development.  The number of plasma cells goes down after a few weeks  Antibodies stay in the blood longer but eventually their numbers go down too.
  • 27. 05/30/11 22:58 T-Lymphocytes  CD3 in all types  CD4 in helper  CD8 in cytotoxic
  • 29. 05/30/11 22:58 Natural killer cells  Large granular lymphocytes  Recognize and destroy cells bedaring viral or tumor surface markers
  • 30. 05/30/11 22:58 Complement Definition : series of heat-labile serum proteins Site : serum and all tissue fluids except urine and CSF Synthesis : in liver – appear in fetal circulation during 1st 13 W Function : Responsible for certain aspects of immune response and inflammatory response Activation : antigen-antibody complex or endotoxin, capsule series of proteins activated sequentially Inactivation: inhibitors in plasma (short lived)
  • 31. 05/30/11 22:58 Complement system  Plasma protein sequence cascade  Triggered by  Classic pathway  Alternative pathway  Lectin binding Complement
  • 32. 05/30/11 05/30/11 22:58 22:58 Complement Activation Complement Activation Classical Pathway Classical Pathway C C1 1 C C4 4 C C2 2 C C3 3 Alternative pathway Alternative pathway C C5 5 C C6 6 C C7 7 C C8 8 C C9 9 Membrane damage Membrane damage
  • 33. 05/30/11 05/30/11 22:58 22:58 Classic And Alterenative pathways Classic And Alterenative pathways Classic Pathway Alternative pathway Classic Pathway Alternative pathway * Specific acquired immunity * Non-specific innate immunity * Specific acquired immunity * Non-specific innate immunity * Initiated by antibody * Bacterial endotoxin, capsule * Initiated by antibody * Bacterial endotoxin, capsule * Interaction of all components * C1, C4, C2 are by-passed * Interaction of all components * C1, C4, C2 are by-passed * Properdin system not involved * Properdin system is involved * Properdin system not involved * Properdin system is involved
  • 34. 05/30/11 22:58 Complement and disease  Complement difficiency  Difficiency of classic pathway components  C3 difficiency  Terminal complement protein difficiencies  Difficiency of regulatory proteins  Heriditary angioedema  PNH  Complement consumption as in SLE
  • 35. 05/30/11 22:58 Functions of Complement  Biologically active complement products have 3 main functions  Opsonisation …… C3b  Chemotaxis and inflammation……C3a, C5a  Cell lysis……….. C5,C6,C7,C8,C9
  • 39. 05/30/11 22:58 Plasma protein electrophoresis
  • 40. 05/30/11 22:58 Antigens  Antigens are macromolecules that elicit an immune response in the body. The most common antigens are proteins and polysaccharides.  Hapten: incomplete Ag which can be conjugated with a carrier protein to form a complete Ag.
  • 41. 05/30/11 22:58 Cytokines  hormone-like soluble low molecular weight protein molecules that act, generally in a paracrine fashion, to regulate immune responses  They are secreted not only by lymphocytes and macrophages but also by endothelial cells, adipocytes, neurons, glial cells, and other types of cells
  • 42. 05/30/11 22:58 Chemokines  cytokines that regulate cell movement and trafficking; they attract neutrophils and other white blood cells to areas of inflammation or immune response.
  • 43. 05/30/11 22:58 Interferons  are potent cytokines that possess antiviral, immunomodulating, and antiproliferative activities  Interferon-α, Interferon-β & Interferon-γ  Recombinant, natural, and pegylated IFNs currently are available for treatment of  condyloma acuminatum, chronic HCV infection, chronic HBV infection,  Kaposi's sarcoma in HIV-infected patients,  other malignancies,  multiple sclerosis
  • 44. 05/30/11 22:58 Tolerance  It is a specific immunologic unresponsiveness  Unresponsiveness to self antigens is known as auto tolerance
  • 45. 05/30/11 22:58 Tolerance B-cells become tolerant to self by two mechanisms: 1) Clonal deletion Probably while B-cell precursors are in bon marrow 2) Clonal anergy B cells in the periphery  Tolerance in B-cells is less complete than in T-cells  The most autoimmune diseases are mediated by antibodies
  • 46. 05/30/11 22:58 Factors affecting induction of tolerance  Maturity of the immune system  Antigen complexity  Antigen dose  Continuous presence of antigen  Immunosuppressive drugs
  • 47. 05/30/11 22:58 Clinical importance of tolerance  Organ transplantation  Tumor development  Autoimmune diseases
  • 48. 05/30/11 22:58 Autoimmune Diseases  Autoimmune diseases occur due to breakdown of the mechanisms that maintain auto tolerance  Auto-antibodies and self reactive T-cells are produced, resulting in tissue damage by several mechanisms
  • 49. 05/30/11 22:58 References  Lecture notes: Immunology 2010  Essential revision notes for MRCP 2009  Merck manual : online textbook  Kumar & Klark : Clinical Medicine 2009  Other Web Resources & books
  • 53. 05/30/11 22:58 References  Lecture notes: Immunology 2010  Essential revision notes for MRCP 2009  Merck manual : online textbook  Kumar & Klark : Clinical Medicine 2009  Other Web Resources & books
  • 56. 05/30/11 22:58 References  Lecture notes: Immunology 2010  Essential revision notes for MRCP 2009  Merck manual : online textbook  Kumar & Klark : Clinical Medicine 2009  Other Web Resources & books