9: Immunology 2: Vaccination, Hypersensitivity, and Ageing Flashcards

1
Q

Active Immunisation

A

The individual is exposed to pathogen or antigen, these stimulate the immune system, and the body creates its own antibodies

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2
Q

Passive Immunisation

A

 Antibodies are created in one individual and then transferred to another

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3
Q

Toxoid Vaccines

A
  • Bacterial exotoxins that have been inactivated or suppressed via heat or chemicals
  • Highly immunogenic
  • Used for tetanus, botulism and diphtheria
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4
Q

Subunit Vaccines

A
  • Contains the particular antigenic determinant of the pathogen
  • Non-living so very safe
  • Poor immuno-memory – limited stimulation of the immune system
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5
Q

Herd Immunity

A
  • The vaccination of a significant enough proportion of the population to offer protection to the population as a whole
  • Disruption of the chain of infection
  • The more immune individuals, the lower the chance of contacting an infected individual
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6
Q

Problems with Vaccines: Adverse Effects

A
  • Allergy to preservatives
  • Reversion to virulence
  • Local hypersensitivity reactions (toxoids)
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7
Q

Innate Immune Cells that Drive Hypersensitivity: Basophils

A

Activated function:

Promotion of allergic responses and augmentation of anti-parasitic immunity

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8
Q

Innate Immune Cells that Drive Hypersensitivity: Mast Cells

A

Release of granules containing histamine and active agents

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9
Q

Innate Immune Cells that Drive Hypersensitivity: Eosinophils

A

Killing of antibody-coated parasites

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10
Q

Hypersensitivity: Type I - Allergy

A
  • Most common type
  • Rapid onset, short-term
  • Local or systemic
  • Induced by antigens (allergens) which activate B-cells to secrete antibodies
  • Antibodies secreted are of the IgE type (usual antibody secretion is IgG or IgM)
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11
Q

Hypersensitivity: Type II - Cytotoxic

A
  • Antibody-mediated cellular destruction
  • May induce direct cellular lysis (complement-mediated)
  • Antibodies may enhance phagocytic activity
  • Examples: ABO transfusion reaction, rhesus incompatibility, drug-induced haemolytic anaemia
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12
Q

Hypersensitivity: Type III - Immune Complex-Mediated

A
  • Accumulation of antibody-antigen complexes in the circulation and tissues
  • Effects depend on location of complexes, but they attract phagocytes – release of lytic enzymes and cytokines and activate complement
  • Can be local or systemic
  • Examples: serum sickness, rheumatoid arthritis, drug reactions
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13
Q

Hypersensitivity: Type IV - Delayed Type

A
  • Delay is 1-3 days (generally peaks 48-72 hours after exposure)
  • Not antibody-mediated but cell-mediated – produced by T-cells interacting with antigens
  • Delayed because specific T-cells must migrate to location of antigen before inflammation develops
  • May be prolonged & result in formation of granulomas e.g. tuberculosis
  • Examples: contact dermatitis
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14
Q

How Does Ageing Affect Immune Function? (Four Effects)

A
  1. Greatly reduced production of thymic hormone (important for the maturation of T-cells)
  2. Reduced responsiveness of T-cells to antigens
  3. Reduced responsiveness of B-cells
  4. Decline in immune surveillance
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15
Q

Ageing and Immune Cells

A
  • Macrophages, neutrophils, and natural killer cells decline in function
  • Leads to deficiencies in innate immunity & increased incidence of cancers due to decline in immune surveillance
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16
Q

Ageing and Cell-Mediated Immunity

A
  • Involution of the thymus gland – by age 50 it is about 15% of maximum size
  • Reduction in levels of thymic hormones results in decreased responsiveness of cytotoxic T-cells to antigen
  • Numbers of CD4 + T-helper cells also reduced with consequent loss of helper function
17
Q

Ageing and Humoral Immunity

A
  • Overall B-cell function compromised, so antibody production reduced & slower
  • Effectiveness of vaccination decreases
  • Affinity of antibody for antigen is reduced
  • Increased levels of autoantibodies – autoimmune disease more prevalent in the aged