Immunisation Flashcards
what is the aim of vaccination
to control communicable diseases
primary prevention
prevent disease onset
what is primary prevention in most circumstances
pre-exposure
secondary prevention
alter course of disease to prevent/limit consequences
eg immunoglobulins to help protect people or interruption of transmission
which antibodies are involved in primary and secondary infection
IgM = first

active immunity
- permanent?
protection produced by the person’s own immune system
usually permanent
can be stimulated by vaccine or naturally acquired infection
how does secondary and subsequent exposure to antigen compare to primary
is more rapid and aggressive as memory cells are present in greater numbers than parent lymphocyte, have already undergone class Ig switching and have enhanced properties of cell adhesion and chemotaxis
passive immunity
- 4 examples
achieved by administering preformed antibodies against a specific antigen
immediate protection of short duration
eg mother to baby, person to animal and injection of human Ig or anti-toxin
which Ig crosses the placenta
IgG
what does mother to baby passive immunity work better/worse for
better - tetanus (this is why pregnant mothers must have tetanus injection) and measles
worse- pertussis, polio and whooping cough
for which diseases would you inject Ig
Hep B, rabies and VZ
for which diseases would you give anti-toxin
diptheria, botunilinum
advantages of passive immunity
rapid action, post exposure, can attentuate illness, limit outbreak, used if contraindication to vaccine
disadvantages of passive immunity
Short term protection, short time effective window, blood derived, hypersensitivity reaction, expensive
herd immunity
protect unvaccinated individuals indirectly through a large proportion of the community being protected by vaccine
in herd immunity, what does the required proportion of unvaccinated individuals depend on
transmissibility and infectiousness of organism and social mixing in the population - basic reproduction rate (R0) (the number of secondary infections produced by a typical case of infection in a population that is totally susceptible)
there must be no reservoir of infection outside of humans
herd immunity and the measles virus
it is very infectious so over 90% of population must be vaccinated in order to achieve herd immunity
how much of the population must be vaccinated for Mumps and Smallpox to achieve herd immunity
80%
live vaccines
contain organisms with attenuated virulence, which results in a fully integrated T lymphocyte and humoral response
eg measles, mumps, rubella (MMR), VZV, rotavirus, flu
who should use of live vaccines in be carefully considered
IC individuals
polio vaccine
inactivated vaccine of inactivated virus
inactivated vaccines
consist of whole killed organisms or their antigenic components
inactivated vaccine: suspension of whole killed organism
whole cell pertussis (whooping cough)
inactivated vaccine: subunit vaccine
only contain the antigenic part of the antigen
inactivated vaccine: toxoid vaccine
based on the toxin produced by certain bacteria
indiviudal may clear toxin but remain a carrier of the organism
eg diptheria and tetanus
inactivated vaccine: conjugate vaccines
polysaccharide attached to immunogenic protein
activate T lymphocytes which results in a sustained response and immunological memory
eg H. influenzae, Neissera meningitidis
what are the contra indications to vaccination
- Confirmed anaphylaxis reaction to previous dose or component of the vaccine
- Live vaccines should not be given to immunosuppressed (high dose steroids, HIV etc.), pregnant women, or in the presence of acute infection
- Severe latex allergy
- Acute/evolving illness
which vaccine are those with egg allergy contra indicated to
yellow fever and flu (if they had more than hives reaction to egg)
what are not contra-indications to vaccination that are often thought of being
Hay fever, asthma, eczema, sickle-cell disease, topical corticosteroid therapy, antibiotic therapy, prematurity and chronic heart and lung diseases (including TB)
UK ROUTINE VACCINATION SCHEDULE
2 months
pneumococcal disease - PCV
rotavirus
diptheria, tetanus, whooping cough, polio and H. influenzae type B= 5 in 1 vaccine
MenB
UK ROUTINE VACCINATION SCHEDULE
3 months
diptheria, tetanus, pertussis, polio, HiB (5 in 1 vaccine)
meningococcal group C
rotavirus
UK ROUTINE VACCINATION SCHEDULE
4 months
diptheria, tetanus, pertussis, polio, HiB (5 in 1 vaccine)
pneumococcal disease - PCV
MenB
UK ROUTINE VACCINATION SCHEDULE
first birthday
Hib MenC
pneumococcal
measles, mumps, rubella (MMR)
MenB
UK ROUTINE VACCINATION SCHEDULE
2,3,4
infleunza
UK ROUTINE VACCINATION SCHEDULE
3y4m or after
diptheria, tetanus, polio and pertussis
MMR
UK ROUTINE VACCINATION SCHEDULE
girls 12-13y
cervical cancer caused by HPV types 16 and 18
and also genital warts caused by types 6 and 11
UK ROUTINE VACCINATION SCHEDULE
14 y
tetanusm diptheria and polio
MenC
UK ROUTINE VACCINATION SCHEDULE
from 28w of pregnancy
pertussis
UK ROUTINE VACCINATION SCHEDULE
65y
pneumococcal disease - PPV
UK ROUTINE VACCINATION SCHEDULE
≥65y
influenza
UK ROUTINE VACCINATION SCHEDULE
70y
shingles
what does the 5 in 1 vaccine cover and at what ages is it given in UK
diptheria, tetanus, pertussis, polio and HiB
DTaP/IPV/Hib
2,3,4 months
diphtheria
- An URT illness characterised by sore throat, low-grade fever, and an adherent pseudomembrane (a layer of exudate resembling a membrane) that can cover the tonsils and the mucosa of the pharynx, larynx, and nose.
- The toxin causes tissue necrosis and formation of the pseudomembrane. It also causes the major complications of myocarditis and neuritis.

what is diphtheria caused by
Corynebacterium Diphtheriae
aerobic Gram positive bacterium
what are the 3 phases of determining a suitable vaccine
safe?
how reactogenic is it? (what dose should be given and how does it compare to other vaccines?)
is it efficacious, and are there any rarer reactions?
yellow card scheme
way of passive reporting used for suspected adverse drug reactions etc
define elimination of disease
reducing incidence to 0 within defined geographical area as a result of deliberate efforts, continued intervention measures required
define eradication of disease
permanent reduction to 0 of worldwide incidence of infection as a result of deliberate efforts, intervention measures no longer required eg small pox
define extinction of disease
the specific infectious agent no longer exists in the nature or laboratory
there are no examples
UK VACCINATION SCHEDULE
when do you get MMR
within a month of first birthday and 3y4m or soon after
UK VACCINATION SCHEDULE
when do you get rotavirus
2 and 3 months
UK VACCINATION SCHEDULE
when do you get HPV
girls aged 12-13 years
UK VACCINATION SCHEDULE
influenza
2, 3, 4 years old
>65 years
UK VACCINATION SCHEDULE
Men C
3m
within month of 1st birthday with Hib
14y
UK VACCINATION SCHEDULE
pneumococcal
2 and 4 months
first birthday
65 years
MenACWY vaccine
MenACWY vaccine protects against meningitis (caused by meningococcal disease types A, C, W and Y bacteria. Given at 14 years and new university students aged 19-25
UK ROUTINE VACCINATION SCHEDULE when do you get Men B
2 months, 4 months and 12-13 months