Professional Documents
Culture Documents
3000BC 1500BC
1700AD
2000BC
Introduction of
Sniffing of small variolation in England
pox crust in China and later in the US
2
Introduction
Introduction of
of variolation
variolation
The
The wife
wife ofof the
the British
BritishAmbassador
Ambassador in in
Turkey,
Turkey, inin March
March 1717 1717 wrote,
wrote, following
following
the
the variolation
variolation of of her
her son,
son, to
to aa friend
friend inin
England:
England: TheThe small
small pox,
pox, so
so fatal,
fatal, so
so general
general
amongst
amongst us, us, isis entirely
entirely harmless
harmless herehere
by
by the
the invention
invention of of ingrafting.I
ingrafting.I am am
patriot
patriot enough
enough to to bring
bring this
this invention
invention intointo
fashion
fashion in in England.
England.
3
Milestones
Milestones in
in immunization
immunization
1780AD
Edward Jenner discovers
small pox vaccine
4
Edward Jenner
6
Modern
Modern era
era of
of the
the vaccine
vaccine
1885 1934
Rabies vaccine Pertussis
(Pasteur)
1920s 1955
Diphtheria and Salk polio
Tetanus
7
Modern
Modern era
era of
of the
the vaccine
vaccine
1960s 1985
Mumps measles Haemophilus
and rubella virus
Sabin polio
1990s
Hepatitis and
varicella
8
Pre-
Pre- &
& post-vaccine
post-vaccine incidence
incidence of
of
common
common preventable
preventable diseases
diseases
9
Different
Different modes
modes of
of acquiring
acquiring
immunity
immunity
Immunity
Natural Acquired
resistance
Passive Active
10
Passive
Passive Immunity
Immunity
Natural Artificia
l
Placental Antibodies or
transfer of IgG immunoglobulins
11
Passive
Passive Immunization
Immunization
12
Advantages
Advantages and
and Disadvantages
Disadvantages
of
of Passive
Passive Immunization
Immunization
Advantages Disadvantages
no long term
protection
serum sickness
immediate
protection risk of hepatitis
and Aids
graft vs. host
disease (cell
graft only)
13
Active
Active Immunization
Immunization
Natural Artificial
Attenuated
organisms
killed organisms
exposure to sub- sub-cellular
clinical infections fragments
toxins
others
14
Live
Live Attenuated
Attenuated Vaccines
Vaccines
polio* hepatitis A
not used in std. not required in
schedule SC
measles, mumps yellow fever
& rubella Military and travelers
Varicella zoster
tuberculosis
children with no
not used in this
history of chicken pox country
15
Killed
Killed Whole-Organism
Whole-Organism Vaccines
Vaccines
polio Q fever
population at risk
influenza typhoid, cholera, plague
elderly and at risk epidemics and travelers
rabies pertussis
post exposure replaced by the
acellular vaccine
16
Microbial
Microbial Fragment
Fragment Vaccines
Vaccines
Bordetella. Pertussis
virulence factor protein
Haemophilus influenzae B
protein conjugated polysaccharide
Streptococcus pneumoniae
Polysaccharide mixture
Neisseria meningitidis
polysaccharide
17
Microbial
Microbial Fragment
Fragment Vaccines
Vaccines
Corynebacterium diphtheriae
inactivated toxin (toxoid)
Vibrio cholerae
toxin subunits
Hepatitis B virus
cloned in yeast
18
Modification
Modification of
of Toxin
Toxin to
to Toxoid
Toxoid
Toxin Toxoid
chemical
modification
19
Future
Future Vaccines
Vaccines
anti-Idiotype Vaccine
DNA
Immuno-dominant peptide
20
Recommended Childhood
Immunization Schedule
21
Adverse
Adverse Events
Events Occurring
Occurring
Within
Within 48
48 Hours
Hours DTP
DTP of
of Vaccination
Vaccination
Event Frequency
local
redness, swelling, pain 1 in 2-3 doses
systemic: Mild/moderate
fever, drowsiness, fretfulness 1 in 2-3 doses
vomiting
anorexia 1 in 5-15 doses
systemic: more serious
persistent crying, fever 1 in 100-300 doses
collapse, convulsions 1 in 1750 doses
acute encephalopathy 1 in 100,000 doses
permanent neurological deficit 1 in 300,000 doses
22
Adverse
Adverse event
event occurring
occurring
within
within 48
48 hours
hours DTP
DTP vaccination
vaccination
Event Frequency
Local:
redness, swelling, pain 1 in 2-3 doses
Mild/moderate systemic:
fever, drowsiness, fretfulness vomiting, 1 in 2-3 doses
anorexia 1 in 5-15 doses
23