7- Infectious diseases Flashcards

1
Q

what are vaccines

A

Substance that stimulates the production of antibodies and provides active immunity against one or several diseases.

  • Prepared from causative agent of a disease, its products or synthetic substitute.
  • Treated to act as an antigen without inducing the disease.
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2
Q

Active immunity

A
  • Protection produced by individual’s own immune system.
  • Acquired by natural disease or vaccination.
  • Usually long lasting.
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3
Q

Passive immunity

A
  • Protection provided by transfer of antibodies from immune individuals.
  • Protection temporary – commonly for only weeks or months.
  • e.g. RSV (Palivizumab), Varicella (ZIG), also measles, tetanus and rabies.
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4
Q

types of vaccine

A
  • inactivated
  • subunit and conjugate vaccines
  • live attenuated
  • toxin vaccine
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5
Q

Inactivated vaccines

A

involve giving a killed version of the pathogen. They cannot cause an infection and are safe for immunocompromised patients, although they may not have an adequate response. Examples are:

  • Polio
  • Influenza vaccine
  • Hepatitis A
  • Rabies
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6
Q

Subunit and conjugate vaccines

A

only contain parts of the organism used to stimulate an immune response. They also cannot cause infection and are safe for immunocompromised patients. Examples of subunit and conjugate vaccines are:

  • Pneumococcus
  • Meningococcus
  • Hepatitis B
  • Pertussis (whooping cough)
  • Haemophilus influenza type B
  • Human papillomavirus (HPV)
  • Shingles (herpes-zoster virus)
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7
Q

Live attenuated vaccines x

A

Live attenuated vaccines contain a weakened version of the pathogen. They are still capable of causing infection, particularly in immunocompromised patients. The following vaccines are live attenuated vaccines:

  • Measles, mumps and rubella vaccine: contains all three weakened viruses
  • BCG: contains a weakened version of tuberculosis
  • Chickenpox: contains a weakened varicella-zoster virus
  • Nasal influenza vaccine (not the injection)
  • Rotavirus vaccine
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8
Q

Toxin vaccines

A

contain a toxin that is normally produced by a pathogen. They cause immunity to the toxin and not the pathogen itself.
Examples are the diphtheria and tetanus vaccines.

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9
Q

BEWARE
Vaccines containing egg:

A
  • Live influenza (Fluenz)
  • Yellow fever
  • Rabies

NOT MMR (but beware if immunosuppressed-inactivated)

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10
Q

routine vaccine schedule summary

A
  • 8 weeks
  • 12 weeks
  • 16 weeks
  • 1 year
  • yearly from age 2-8
  • 3 years 4 months
  • 12-13 years
  • 14 years
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11
Q

8 weeks

A
  • 6 in 1 vaccine (diphtheria, tetanus, pertussis, polio, haemophilus influenzae type B (Hib) and hepatitis B)
  • Meningococcal type B
  • Rotavirus (oral vaccine)
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12
Q

12 weeks:

A
  • 6 in 1 vaccine (again)
  • Pneumococcal (13 different serotypes)
  • Rotavirus (again)
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13
Q

16 weeks:

A
  • 6 in 1 vaccine (again)
  • Meningococcal type B (again)
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14
Q

1 year:

A
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15
Q

Yearly from age 2 – 8:

A
  • Influenza vaccine (nasal vaccine)
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16
Q

3 years 4 months:

A
  • 4 in 1 (diphtheria, tetanus, pertussis and polio)
  • MMR vaccine (again)
17
Q

12 – 13 years:

A
  • Human papillomavirus (HPV) vaccine (2 doses given 6 to 24 months apart)
18
Q

14 years:

A
  • 3 in 1 (tetanus, diphtheria and polio)
  • Meningococcal groups A, C, W and Y
19
Q

BCG

A

BCG
- Offered from birth to babies are higher risk of TB
- E.g. with relatives from countries with high TB prevalence or who live in urban areas with high rate of TB
- May also be given to children arriving from areas of high TB prevalence or those in close contact with those with it

20
Q

Human papilloma virus- GARDASIL

A

Aim to give to boys and girls before they become sexually active- reduces risk of cervical cancer
* Strains 6 and 11 cause genital warts
* Strains 16 and 18 cause cervical cancer

21
Q

Toxoid vaccines (PTD): Diptheria

A
  • Corynebacterium diphtheria
  • Disappeared from the UK now
22
Q

Toxoid vaccines: tetanus

A

clostridium tetani

23
Q

toxoid vaccine: whooping cough

A

Bordetella pertussis

  • Pertussis is always present in the community.
  • Continued infectious risk because:
    –> Infection does not provide lifelong immunity.
    –> Vaccination protection lasts for about 6 years.
  • Current acellular vaccine* replaced cellular vaccine in early 2000s.
    –>Protection afforded by acellular vaccine wears off more quickly.
    –>Has lower incidence of side-effects.
  • Vaccination programme changes:
    –>Infants very vulnerable before vaccinations start (<2 months).
    –>UK policy of maternal vaccination at 28-32 weeks – to protect infants not themselves
24
Q

killed birus: Poliomyelitis

A
  • Poliovirus
  • Enterovirus
  • Lower motor neurone disease- affects single dermatomes
  • Old virus was live: caused paralytic polio
  • Now killed virus
25
Q

Subunit and conjugate vaccines: Hep B

A
26
Q

Subunit and conjugate vaccines: Haemophilus influenzae type b

A
27
Q

Subunit and conjugate vaccines: pneumonococcal disease

A
28
Q

Subunit and conjugate vaccines: meningococcaemia (neisseria meningiditis)

A
29
Q

live attenuated: rota virus

A
30
Q

live attenutated: MMR Rubella

A

Togavirus

31
Q

live attenutated: MMR Mumps

A

paramyxovirus

32
Q

live attenutated: MMR measles

A

morbillivirus