Immunology - Viral Diseases Flashcards

1
Q

Immunisation

A

The process whereby a susceptible individual is rendered immune to an infection
Can be passive or active
Aims of immunisation can range from eradication to preventing symptoms

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2
Q

Passive immunisation

A

Transfer of pre-formed antibodies to a susceptible individual giving temporary protection from infection

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3
Q

Natural, passive immunisation

A

Mother to baby via the placenta and breast milk

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4
Q

Diseases requiring normal immunoglobulins - passive immunisation

A

Hep A

Measles

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5
Q

Diseases requiring spp immunoglobulins - passive immunisation

A

Hep B
Rabies
Varicella Zoster
Tetanus

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6
Q

Diseases requiring monoclonal immunoglobulins - passive immunisation

A

RSV

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7
Q

Molecules used in active immunisation

A
Live attenuated
Inactivated whole cell 
Toxoid 
Subunit 
Polysaccharides 
Conjugated polysaccharide
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8
Q

Live attenuated vaccines

A

Traditionally generated by serial passage in tissue culture

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9
Q

Examples of live attenuated vaccines

A
TB (BCG)
Measles 
Mumps
Rubella
Varicella Zoster
Rotavirus
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10
Q

Pros of live attenuated vaccines

A

Replicates in recipients = excellent immune response

More closely resembles natural infection = mucosal immunity as appropriate

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11
Q

Cons of live attenuated vaccines

A

Potential for reversion
Potential for sustained vaccine strain infection
Not suitable for all

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12
Q

Inactivated whole cell vaccines

A

Pathogen killed by chemical or physical processes

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13
Q

Examples of inactivated whole cell vaccines

A

Inactivated polio (Salk)
Hep A
Rabies

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14
Q

Toxoid vaccine

A

Inactivated toxin

Toxins chemically treated to eliminate toxicity whilst maintaining immunogenicity e.g. w/ formaldehyde

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15
Q

Examples of toxoid vaccines

A

Diphtheria

Tetanus

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16
Q

Types of subunit vaccines

A

Recombinant proteins

Chemically purified

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17
Q

Subunit vaccines - recombinant proteins

A

Spp viral protein produced in a heterologous expression system

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18
Q

Recombinant proteins examples

A

Hep B

Papillomavirus

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19
Q

Subunit vaccines - chemically purified

A

Certain components of a pathogen are purified for use in a vaccine

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20
Q

Examples of chemically purified subunit vaccines

A

Acellular pertussis

Influenza

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21
Q

Polysaccharide vaccines

A

Purified bacterial polysaccharide

T cell independent and poorly immunogenic in young children

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22
Q

Examples of polysaccharide vaccines

A

Some meningococcal vaccines
Some pneumococcal vaccines
Salmonella

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23
Q

Conjugated polysaccharide vaccines

A

Purified bacterial polysaccharide linked to a protein

24
Q

Examples of conjugated polysaccharides

A

H. influenzae
Pneumococcal
Meningococcal

25
Adjuvants
Agents that stimulate the immune system | Thought to sequester antigen and cause infl
26
Commonly used adjuvants
Aluminium phospahte | Aluminium hydroxide
27
Pre exposure vaccines in adults
65 yrs of age - pneumococcal polysaccharide vaccines 65 yrs of age - annual influenza vaccine 70 yrs of age - varicella zoster (shingles)
28
Pre exposure vaccines in pregnant women
Influenza vaccine in any trimester prior to start of flu season Pertussis vaccine from 16 weeks' gestation
29
Childhood vaccines at 2 months
Diphtheria/ tetanus/ pertussis/ polio/ haemophilus/ hep B Meningococcal B Rotavirus
30
Childhood vaccines at 3 months
Diphtheria/ tetanus/ pertussis/ polio/ haemophilus/ hep B Rotavirus Pneumococcal conjugate
31
Childhood vaccines at 4 months
Diphtheria/ tetanus/ pertussis/ polio/ haemophilus/ hep B | Meningococcal B
32
Childhood vaccines at 12-13 months
Haemophilus/ meningococcal C conjugate Meningococcal B Pneumococcal conjugate MMR
33
Childhood vaccines at 2 years
Influenza - annually to age 16 (in process of being rolled out)
34
Childhood vaccines at 3yr 4 months
Diphtheria/ tetanus/ pertussis/ polio | MMR
35
Childhood vaccines at 12-13 yrs
Papillomavirus (2 doses 6 months apart)
36
Childhood vaccines at 14 years
Tetanus/ diphtheria/ polio | Meningococcal ACWY conjugate
37
Post-exposure vaccines
Ig and some vaccines can be given after exposure to reduce the chance of an individual developing a disease of reducing disease severity
38
Examples of post-exposure vaccines
Wounds at risk of tetanus - spp Ig Potential rabies exposure - course of vaccine +/- -spp Ig Unvaccinated contact w/ confirmed measles case - vaccine, in contraindicated - consider normal Ig
39
Adverse effects to immunisations
Related to either immunogenicity or other component of the vaccine Most commonly local reactions - pain, swelling and redness General systemic effects - fever, headaches and malaise
40
Examples of adverse effects to immunisations
Yellow fever - encephalitis Rubella - thrombocytopenia BCG - osteitis Rotavirus - potential increased risk of intussusception
41
Contraindications considerations for immunisations
Hx of anaphylaxis to previous vaccine/ vaccine component Immunosupression Pregnancy
42
When may an immunisation need to be deferred
Acutely unwell Other vaccines given recently Ig therapy
43
Immunisation failure
Primary vaccine failure | Secondary vaccine failure
44
Primary vaccine failure
Failure to mount an immune response to a vaccine
45
Causes of primary vaccine failure
Vaccine factors Host factors Inappropriate vaccine schedule
46
Vaccine factors leading to primary vaccine failure
Administration error Manufacturing error Incomplete strain coverage
47
Host factors leading to primary vaccine failure
Immunodeficiency | Immunological issues
48
Secondary vaccine failure
Immunity develops initially following immunisation but w/ time immunity wanes
49
What does the innate immune system rely on
Interaction between PRR's and PAMPs
50
What does the innate immune system comprise
Mechanical barrier Proteins (enzymes, complement) Cells (macrophages, neutrophils, NK cells)
51
What does the adaptive immune system comprise
``` B cells - antibody production T cells (CD4 - 'helper' cels and CD8 - 'cytotoxic' cells) ```
52
Why do we need 2 vaccines for live attenuated virus vaccines
We go from sero-ve to seroprotective but the virus-app antibody titre drops so we become sero+ve, therefore requiring a booster
53
Sero+ve
Partial or no protection
54
Why don't wild - type viruses require a booster
Despite virus-app antibody titre drops, it is still enough to be seroprotective
55
Why might a child not have been vaccinated
Parents may have refused | Vaccination may have been accidentally missed
56
Examples of misinformation about immunisations
Polio (a Western plot to make African women infertile) | HPV (a cause of promiscuity in teenagers)