Immuno: Immune modulating therapies Pt.1 Flashcards

1
Q

List some approaches to boosting the immune system.

A
  • Vaccination
  • Replacement of missing components (e.g. replacing immune cells)
  • Cytokine therapy
  • Blocking immune checkpoints
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2
Q

What happens when cells of the adaptive immune system engage with an antigen that it recognises?

A

Becomes activated - will proliferate and differentiate

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3
Q

What happens to T-cells when activated?

A

Proliferate and differentiate into effector cells (cytokine secreting, cytotoxic)

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4
Q

What are the two ways in which B cells can undergo clonal expansion once activated?

A
  • They can differentiate into T-cell independent IgM plasma cells
  • They can undergo a germinal centre reaction (T cell dependent) and become IgG/A/E memory and plasma cells
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5
Q

Which type of T cell undergoes a more pronounced proliferation following activation?

A

CD8 > CD4

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6
Q

List three types of antigen-presenting cell.

A
  • Dendritic cells
  • Macrophages
  • B lymphocytes
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7
Q

What are some important characteristics of memory cells?

A

Longevity

  • Memory T cells persist for a long time in the absence of antigen due to low level continual proliferation in response to cytokines

Different pattern of cell surface proteins involved in chemotaxis cell adhesion

  • Allows memory cells to rapidly access non-lymphoid tissues

Rapid, robust response to subsequent antigen exposure

  • Memory cells are more easily activated than naive cells
  • B cell memory involves that circulation of pre-formed high-affinity IgG antibodies
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8
Q

What are the aims of vaccines?

A
  • MEMORY – preformed antibodies, memory T cells, memory B cells, to provide long-lasting, protective immunity
  • No adverse reactions
  • Practical considerations – one shot, easy storage, inexpensive
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9
Q

Which cell surface receptor is used in the influenza vaccine?

A

Haemagglutinin (HA) - this is a receptor-binding and membrane fusion glycoprotein

ie. the reason influenza can infect cells

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10
Q

What are haemagglutination assays used for?
Describe how do they work.

A

Used to detect viral antibodies

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11
Q

How long does protection from the influenza vaccine last?

A

Starts 7 days after the vaccine and protection lasts for 6 months.

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12
Q

What agent is used in the BCG vaccine?

A

Attenuated strain of Mycobacterium bovis.

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13
Q

Describe the protection that is achieved by using the BCG.

A
  • Some protection against primary infection
  • Mainly protects against progression to active TB

NOTE : T cell response is important in protection against primary and progression to active TB

NOTE: protection lasts for 10-15 years

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14
Q

What is the Mantoux test?

A
  • A small amount of liquid tuberculin (PPD) is injected intradermally
  • The area of injection is examined 48-72 hours after the injection
  • A reaction would appear as a wheel around the injection site (this is suggestive of latent TB, active TB or previous BCG)
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15
Q

What is a live attenuated vaccine? List some examples.

A

The organism is alive but modified to limit its pathogenesis.
V-BOY

Examples:

  • MMR,
  • Varicella zoster,
  • BCG,
  • Oral polio (Sabin)
  • Yellow fever,
  • nasal influenza, typhoid,
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16
Q

List some advantages of live attenuated vaccines.

A
  • Raises broad immune response to multiple antigens – more likely to protect against different strains
  • Activates all phases of immune system. T cells, B cells – with local IgA, humoral IgG
  • May confer lifelong immunity, sometimes just after one dose
17
Q

List some disadvantages of live attenuated vaccines

A

Possible reversion to virulence (recombination, mutation).

  • Vaccine associated paralytic poliomyelitis (VAPP, ca. 1: 750,000 recipients)
  • Spread to contacts (immunosuppressed patients)
  • Storage problems
18
Q

List some examples of inactivated vaccines

A
  • Inlfuenza (quadrivalent)
  • Cholera
  • Polio (Salk)
  • Hep A
  • Pertussis
  • Rabies
19
Q

List some examples of the following types of vaccine:

  1. Toxoids
  2. Component/Subunit
A
  1. Toxoids (inactivated toxins)
    • Diphtheria
    • Tetanus
  2. Component/Subunit
    • Hep B (HBsAg)
    • HPV (capsid)
    • Influenza (HA)
20
Q

What are the advantages of inactivated/component vaccines?

A
  • No risk of reversion to virulent form
  • Can be used with immunodeficient patients
  • Storage easier
  • Lower cost
21
Q

What are some disadvantages of inactivated/component vaccines?

A
  • Often do not follow normal route of infection (reduced local protection)
  • Some components have poor immunogenicity
  • May need multiple injections
  • May require modification to enhance immunogenicity e.g. conjugate to protein carrier, adjuvant
22
Q

Describe how conjugate vaccines work.

A

Polysaccharide and protein carrier

  • Polysaccharides weakly immunogenic - induces a T-cell independent B cell response (transient)
  • Addition of the protein carrier promoted T cell immunity which enhances B cell/antibody responses