Lecture 3 - Immunisation and immunotherapy Flashcards

1
Q

Briefly describe how active immunisation works

A

administering antigen induces antibody and/or T cell response specific to the given antigen. Both systemic and mucosal immunity can be induced. protection not immediate

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2
Q

Briefly describe how passive immunisation works

A

administer pre formed antibody in order to protect from disease. immediate protection but no immunological memory or immune response generated

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3
Q

Which immunoglobulins are generated at each stage of antibody responce

A

primary is IgM and secondary is mainly igG

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4
Q

Describe a live attenuated vaccination

A

one dose of organism who’s virulance has been reduced - organism multiplys in host and immune response same as that of natural infection.
systemic and mucosal

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5
Q

Describe the risks of a live attenuated vaccine

A
  • severe infection in immunocompromised
  • organism can revert to normal virulence
  • storage conditions are critical
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6
Q

3 examples of a live attenuated vaccine

A

MMR, BCG, oral polio

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7
Q

Describe a killed vaccination

A

several doses of inactivated organism - immune response generated. only systemic reaction
stable to store. have to administer with adjunctive which boost immune system

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8
Q

Give and example of an adjunctive used in vaccination

A

aluminium hydroxide - NOT antigens

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9
Q

Name the risks of a killed vaccination

A
  • risk of reaction

- the inactivated form may change the structure of the organism

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10
Q

Give 3 examples of killed vaccination

A

killed polio, influenza, pertussis

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11
Q

Describe a subunit vaccination

A

parts of an organism are administered in several doses with adjuvant. usually only a systemic response. body doesn’t mimmic natural response but does induce response to prevent disease

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12
Q

Give 4 examples of a subunit vaccination

A

Gr C menningococcal, tettanus, Hep B, hib

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13
Q

Describe subunit conjugate vaccinations

A

two subunits are bound in order to activate both B cells and T cells. B cells cannot divide unless activated by T cells. e.g. diptheria protein and mennincococcal Gr C polysacharide

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14
Q

Describe some contraindications for vaccines

A
  • acute illness or allergy to previous doses
  • live vaccines shouldn’t be used in pregnancy or in immunocompromised (primary e.g. HIV or secondary e.g. steroids chemo)
  • allergy to stuff in vaccine e.g. influenza vaccine made with extracts of egg
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15
Q

When should live vaccine doses be given and why

A

at the same time or several weeks apart (too close together and immune system is suppressed and wont respond to second dose)

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16
Q

Which vaccine cant you give if the patient is on antibiotic therapy

A

typhoid

17
Q

Which vaccine is given to splenectomy patients and why?

A

pneumovax against pneumococcus. no spleen increases susceptibility

18
Q

What is Human immunoglobulin replacement therapy ?

A

IgGs derived from plasma of 1000 doners. must be 90% intact. must be biologically active and must no have any inflammatory mediators or infectious agents.

19
Q

What is in commercial IVIG

A

lots of antibodies from lots of bacteria/virus’

still active to neutralise toxins and activate compliment

20
Q

When would commercial IVIG be given?

A

Primary immunodeficiencies:
-B cells e.g. x linked agammaglobulinaemia or hyper igM
-T cell deficiency (as activates)
Secondary immunodeficiencies:
- chronic lymphocytic leukaemia or multiple myeloma
- HIV in children with recurrent infections
- premature babies with recurrent infections
- early onset neonatal sepsis

21
Q

How are specific immunoglobulin preparations produced in replacement Ig therapy

A

either plasma pre screened for high titres of antibody

or volunteers vaccinated first so prod loads of ABs e.g. rabies

22
Q

Give examples of hyperimmune immunoglobulin for post exposure treatment / prophylaxis

A

rabies (bitten), RSV, Hepatitis (e.g. needle stick injury), tetanus, VZV( if mother develops chicken pox within 5 days of birth, CMV if immunosuppressed

23
Q

What are monoclonal antibodies?

A

Artificially produced antibodies of a single specificity derived from a single B cell clone.

24
Q

Name three positives to using monoclonal antibodies

A

endless supply
highly specific and more potent than immune sera
reduce risk of transferring infection

25
Q

Name 4 biological activites of cytokines

A

stimulation of cells in immune system
stimulation of inflammation
stimulation of haematopoiesis
anti-viral and anti-proliferative activities

26
Q

Describe two occasions when interferon alpha therapy is appropriate

A

Hepatitis B - 50% response rate though

Hepatitis C in combination with Ribavirin (or pegintereforon alpha)

27
Q

How does interferon alpha cytokine therapy reduce viral activity

A

inhibiting viral replication and protein synthesis

stimulating antiviral immune responce

28
Q

How are circulating neutrophil levels enhanced in cytokine therapy ? Why is this a benefit and in what?

A

1) granulocytes CSF and granulocytes and macrophages CSF
2) -reduces febrile neutropenia in cytotoxic chemo
- reduces duration of neutropenia in myeloblative therapy followed by BMT

29
Q

Why is interferon gama used in cytokine therapy? example of when this is used and how it works?

A

enhances phagocyte function e.g. in chronic granulomatous disease
- CGD phagocyte NADPH oxidase gene defect therefor reactive oxygen metabolites not generated (needed for killing bac). interferon gama upregs NADPH oxidase