IMMUNOLGY
Study of all biological, chemical,
and physical event surrounding
the function of the immune
system.
Function of the Immune System
(Self/Non-self Discrimination)
• Operates as a surveillance system
• To protect from pathogens
• Intracellular (e.g. viruses and some
bacteria and parasites)
• Extracellular (e.g. most bacteria, fungi
and parasites)
• To eliminate modified or altered self
IMMUNITY
Immune System
Immune System
Innate
(Nonspecific)
Adaptive
(Specific)
Cellular Components Humoral Components Cellular immunity Humoral immunity
Innate Immunity Specific Immunity
Comparison of Innate and Adaptive
Immunity
• No memory
• No time lag
• Not antigen specific
• A lag period
• Antigen specific
• Development
of memory
Innate Host Defenses Against Infection
FIRST LINE OF DEFENCE
• Anatomical barriers–
 Mechanical factors
– Chemical factors
– Biological factors
SECOND LINE OF DEFENCE
• Humoral components–
– Complement
– Coagulation system
– Cytokines
• Cellular components
– Neutrophils
– Monocytes and macrophages
– NK cells
– Eosinophils
Non-Specific Defense Mechanism in Humans
Anatomical Barriers - Biological Factors
System or Organ Component Mechanism
Skin and mucous
membranes
Normal flora Antimicrobial
substances
Competition for
nutrients
Colonization
Anatomical Barriers - Mechanical Factors
System or Organ Cell type Mechanism
Skin Squamous epithelium Physical barrier
Desquamation
Mucous Membranes Non-ciliated epithelium
(e.g. GI tract)
Peristalsis
Ciliated epithelium (e.g.
respiratory tract)
Mucociliary elevator
Epithelium (e.g.
nasopharynx)
Flushing action of
tears, saliva,
mucus, urine
Anatomical Barriers - Chemical Factors
System or Organ Component Mechanism
Skin Sweat Anti-microbial fatty
acids
Mucous Membranes HCl (parietal cells)
Tears and saliva
Low pH
Lysozyme and
phospholipase A
Defensins (respiratory & GI
tract)
Antimicrobial
Sufactants (lung) Opsonin
Humoral Components
Component Mechanism
Complement Lysis of bacteria and some viruses
Opsonin
Increase in vascular permeability
Recruitment and activation of phagocytic cells
Coagulation system Increase vascular permeability
Recruitment of phagocytic cells
Β-lysin from platelets – a cationic detergent
Lactoferrin and
transferrin
Compete with bacteria for iron
Lysozyme Breaks down bacterial cell walls
Cytokines Various effects
Cellular Components
Cell Functions
Neutrophils Phagocytosis and intracellular killing
Inflammation and tissue damage
Macrophages Phagocytosis and intracellular killing
Extracellular killing of infected or altered self
targets
Tissue repair
Antigen presentation for specific immune
response
NK and LAK cells Killing of virus-infected and altered self targets
Eosinophils Killing of certain parasites
PHAGOCYTOSIS
AND
INTRACELLULAR
KILLING
CELLULAR MECHANISM
1) PHAGOCYTIC CELLS
• Neutrophilic polymorphonuclear leucocytes
• Monocytic macrophages( phagocytosis)
2 ) NATURAL KILLER CELLS
• Non phagocytic lymphoid cells
• Lack surface markers
• Damage virus laden tissue cells
• Immunological surveillance against neoplasia
• Characteristic nucleus,
cytoplasm
• Granules
• CD 66 membrane
marker
Phagocytes - Neutrophils (PNMs)
Primary granules
contain cationic proteins,
lysozyme, defensins,
elastase and
myeloperoxidase
Secondary granules
contain lysozyme, NADPH
oxidase components,
lactoferrin and B12-binding
protein
azurophilic;
characteristic of young
neutrophils;
specific for mature neutrophils
Characteristics of Neutrophil
Granules
• Characteristic nucleus
• Lysosomes
• CD14 membrane marker
Phagocytes - Macrophages
PHAGOCYTOSIS
• CHEMOTACTIC FACTORS
• CONTACT AND INGESTION
(PHAGOSOME FORMATION)
• FORMATION OF PHAGOLYSOSOME
• KILLING, DIGESTION OF MICROBES
• RELEASE OF DEBRIS
Attachment via Receptors:
IgG Fc R
Scavenger R
Complement R
Toll-like R
Initiation of Phagocytosis
Phagocytosis
• Attachment
•Pseudopod extension
•Phagosome formation
•Granule fusion
•Phagolysosome formation
Intracellular Killing Pathways
Intracellular Killing
Oxygen
Dependent
Oxygen
Independent
Myleoperoxidase
Dependent
Myleoperoxidase
Independent
Effector Molecule Function
Oxygen-Independent Killing in
the Phagolysosome
Cationic proteins (cathepsin) Damage to microbial
membranes
Lysozyme Hydrolyses mucopeptides
in the cell wall
Lactoferrin Deprives pathogens of iron
Hydrolytic enzymes (proteases) Digests killed organisms
NON-SPECIFIC KILLER
CELLS
NK and LAK cells
ADCC (K) cell
Activated macrophages
Eosinophils
They all kill foreign
and altered self
targets
Natural Killer (NK) cells
also known as large granular
lymphocytes (LGL)
kill virus-infected or
malignant cells
identified by the presence of
CD56 & CD16 and absence
of CD3
activated by IL2 and IFN-γ to
become LAK cells
Lymphokine Activated Killer (LAK)
cell
IL2
IFN
IFN
IL2
kills
malignant
cells
kills
transformed
and malignant
cells
KILLER -K Cells--- ADCC
morphologically undefined
mediate ADCC
have Fc receptor
recognize antibody coated
targets
could be NK cells (IgG),
macrophages (IgG),
eosinophils (IgE) or other cells
(IgG)
Opsonization by IgG Ab by phagocyte
INTERFERON
• Small proteins produced by certain WBC and tissues.
• Three major types: alpha– lymphocytes, macrophages
• beta--- fibroblasts
• gamma—T cells
• USED against viral infections and cancer.
MECHANISM IN VIRUS INFECTED CELL:
• Transcription and translation of IFN gene in infected cell
• IFN diffuses out of infected cells
• Attachment --- specific receptors of un infected cells– enters the
nucleus
• IFN activates genes– synthesis of anti-viral proteins --- BLOCK
viral replication ---
ANTI-VIRAL STATE
• IFN does not prevent virus from entering cells but block viral
replication
ACTION OF INTERFERONACTION OF INTERFERON
Mechanism of alpha and beta Interferon
Ant-viral activity of Interferon
Effects of IFN gamma
ACQURIED SPECIFIC IMMUNITY
• HUMORAL: immune response– B cells stimulated– plasma cells–
Ab (Ig)– destruction extracellular pathogens
• CELLULAR: immune response– T cells sensitized +
macrophages– destruction intracellular pathogens, tumor cells
HUMORAL & CELLULAR CAN BE:
• ACTIVE: Foreign antigens– activate cells of immune system–
Recognition, specificity, destruction, memory
NATURAL- INFECTION
ARTIFICIAL- VACCINATION, IMMUNIZATION
• PASSIVE: preformed antibodies introduced– non immune
person--- protection
NATURAL– TRANSPLACENTAL, BREAST MILK
ARTIFICIAL– GEMMAGLOBULIN, ANTI TOXINS
•
Inate immunity

Inate immunity

  • 1.
    IMMUNOLGY Study of allbiological, chemical, and physical event surrounding the function of the immune system.
  • 2.
    Function of theImmune System (Self/Non-self Discrimination) • Operates as a surveillance system • To protect from pathogens • Intracellular (e.g. viruses and some bacteria and parasites) • Extracellular (e.g. most bacteria, fungi and parasites) • To eliminate modified or altered self
  • 3.
  • 4.
    Immune System Immune System Innate (Nonspecific) Adaptive (Specific) CellularComponents Humoral Components Cellular immunity Humoral immunity
  • 5.
    Innate Immunity SpecificImmunity Comparison of Innate and Adaptive Immunity • No memory • No time lag • Not antigen specific • A lag period • Antigen specific • Development of memory
  • 6.
    Innate Host DefensesAgainst Infection FIRST LINE OF DEFENCE • Anatomical barriers–  Mechanical factors – Chemical factors – Biological factors SECOND LINE OF DEFENCE • Humoral components– – Complement – Coagulation system – Cytokines • Cellular components – Neutrophils – Monocytes and macrophages – NK cells – Eosinophils
  • 7.
  • 8.
    Anatomical Barriers -Biological Factors System or Organ Component Mechanism Skin and mucous membranes Normal flora Antimicrobial substances Competition for nutrients Colonization
  • 9.
    Anatomical Barriers -Mechanical Factors System or Organ Cell type Mechanism Skin Squamous epithelium Physical barrier Desquamation Mucous Membranes Non-ciliated epithelium (e.g. GI tract) Peristalsis Ciliated epithelium (e.g. respiratory tract) Mucociliary elevator Epithelium (e.g. nasopharynx) Flushing action of tears, saliva, mucus, urine
  • 10.
    Anatomical Barriers -Chemical Factors System or Organ Component Mechanism Skin Sweat Anti-microbial fatty acids Mucous Membranes HCl (parietal cells) Tears and saliva Low pH Lysozyme and phospholipase A Defensins (respiratory & GI tract) Antimicrobial Sufactants (lung) Opsonin
  • 11.
    Humoral Components Component Mechanism ComplementLysis of bacteria and some viruses Opsonin Increase in vascular permeability Recruitment and activation of phagocytic cells Coagulation system Increase vascular permeability Recruitment of phagocytic cells Β-lysin from platelets – a cationic detergent Lactoferrin and transferrin Compete with bacteria for iron Lysozyme Breaks down bacterial cell walls Cytokines Various effects
  • 12.
    Cellular Components Cell Functions NeutrophilsPhagocytosis and intracellular killing Inflammation and tissue damage Macrophages Phagocytosis and intracellular killing Extracellular killing of infected or altered self targets Tissue repair Antigen presentation for specific immune response NK and LAK cells Killing of virus-infected and altered self targets Eosinophils Killing of certain parasites
  • 13.
  • 14.
    CELLULAR MECHANISM 1) PHAGOCYTICCELLS • Neutrophilic polymorphonuclear leucocytes • Monocytic macrophages( phagocytosis) 2 ) NATURAL KILLER CELLS • Non phagocytic lymphoid cells • Lack surface markers • Damage virus laden tissue cells • Immunological surveillance against neoplasia
  • 15.
    • Characteristic nucleus, cytoplasm •Granules • CD 66 membrane marker Phagocytes - Neutrophils (PNMs)
  • 16.
    Primary granules contain cationicproteins, lysozyme, defensins, elastase and myeloperoxidase Secondary granules contain lysozyme, NADPH oxidase components, lactoferrin and B12-binding protein azurophilic; characteristic of young neutrophils; specific for mature neutrophils Characteristics of Neutrophil Granules
  • 17.
    • Characteristic nucleus •Lysosomes • CD14 membrane marker Phagocytes - Macrophages
  • 18.
    PHAGOCYTOSIS • CHEMOTACTIC FACTORS •CONTACT AND INGESTION (PHAGOSOME FORMATION) • FORMATION OF PHAGOLYSOSOME • KILLING, DIGESTION OF MICROBES • RELEASE OF DEBRIS
  • 21.
    Attachment via Receptors: IgGFc R Scavenger R Complement R Toll-like R Initiation of Phagocytosis
  • 22.
    Phagocytosis • Attachment •Pseudopod extension •Phagosomeformation •Granule fusion •Phagolysosome formation
  • 24.
    Intracellular Killing Pathways IntracellularKilling Oxygen Dependent Oxygen Independent Myleoperoxidase Dependent Myleoperoxidase Independent
  • 25.
    Effector Molecule Function Oxygen-IndependentKilling in the Phagolysosome Cationic proteins (cathepsin) Damage to microbial membranes Lysozyme Hydrolyses mucopeptides in the cell wall Lactoferrin Deprives pathogens of iron Hydrolytic enzymes (proteases) Digests killed organisms
  • 26.
    NON-SPECIFIC KILLER CELLS NK andLAK cells ADCC (K) cell Activated macrophages Eosinophils They all kill foreign and altered self targets
  • 27.
    Natural Killer (NK)cells also known as large granular lymphocytes (LGL) kill virus-infected or malignant cells identified by the presence of CD56 & CD16 and absence of CD3 activated by IL2 and IFN-γ to become LAK cells
  • 28.
    Lymphokine Activated Killer(LAK) cell IL2 IFN IFN IL2 kills malignant cells kills transformed and malignant cells
  • 29.
    KILLER -K Cells---ADCC morphologically undefined mediate ADCC have Fc receptor recognize antibody coated targets could be NK cells (IgG), macrophages (IgG), eosinophils (IgE) or other cells (IgG)
  • 30.
    Opsonization by IgGAb by phagocyte
  • 32.
    INTERFERON • Small proteinsproduced by certain WBC and tissues. • Three major types: alpha– lymphocytes, macrophages • beta--- fibroblasts • gamma—T cells • USED against viral infections and cancer. MECHANISM IN VIRUS INFECTED CELL: • Transcription and translation of IFN gene in infected cell • IFN diffuses out of infected cells • Attachment --- specific receptors of un infected cells– enters the nucleus • IFN activates genes– synthesis of anti-viral proteins --- BLOCK viral replication --- ANTI-VIRAL STATE • IFN does not prevent virus from entering cells but block viral replication
  • 33.
  • 34.
    Mechanism of alphaand beta Interferon
  • 35.
  • 36.
  • 38.
    ACQURIED SPECIFIC IMMUNITY •HUMORAL: immune response– B cells stimulated– plasma cells– Ab (Ig)– destruction extracellular pathogens • CELLULAR: immune response– T cells sensitized + macrophages– destruction intracellular pathogens, tumor cells HUMORAL & CELLULAR CAN BE: • ACTIVE: Foreign antigens– activate cells of immune system– Recognition, specificity, destruction, memory NATURAL- INFECTION ARTIFICIAL- VACCINATION, IMMUNIZATION • PASSIVE: preformed antibodies introduced– non immune person--- protection NATURAL– TRANSPLACENTAL, BREAST MILK ARTIFICIAL– GEMMAGLOBULIN, ANTI TOXINS •