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

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
Name 4 biological activites of cytokines
stimulation of cells in immune system stimulation of inflammation stimulation of haematopoiesis anti-viral and anti-proliferative activities
26
Describe two occasions when interferon alpha therapy is appropriate
Hepatitis B - 50% response rate though | Hepatitis C in combination with Ribavirin (or pegintereforon alpha)
27
How does interferon alpha cytokine therapy reduce viral activity
inhibiting viral replication and protein synthesis | stimulating antiviral immune responce
28
How are circulating neutrophil levels enhanced in cytokine therapy ? Why is this a benefit and in what?
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
Why is interferon gama used in cytokine therapy? example of when this is used and how it works?
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