Prophylaxis (prevention) and immunizations in childhood. Flashcards
what are the two types of immunisation ?
passive immunisation = giving antibodies against microorganism given for acute prophylaxis
= patient do not produces memory b cells however immunity starts immediately
and active immunisation - involves giving antigenic material into the body
what are the type of active vaccines and examples of them
live vaccines - vaccina virus and vanilla virus = eradicated smallpox vanilla virus ------ live inactivated (attenuated) microorganism = polio (sabin) hep a MMR , BCG varicella zooster , yellow fever rotavirus , influenza pertussis (bacteria) typhoid (bacteria) tuberculosis (bacteria) most successful viral vaccines belongs in this group and the replication of the vaccine produces and immune response = important to store in cool condition ---------
KILLED INACTIVATED VACCINE :
killed micro-organism vaccines - bacteria : typhoid , cholera , pertussis plague
virus
rabies
polio (salk) = preferred in immunocompromised
hep A
subcellular fractions :
surface antigen - hep b
polysaccharide capsules conjugated to protein carriers most effective for immature immune systems -
H influenza type B ,
strep -pneumococcal
neisseria meningitides - meningococcal
toxoids -
tetanus
diphtheria
= however can be a silent career and pass on diseases
recombinant vaccines
hep b
what is a toxoid
bacterial toxin modified to be non toxic but still capable of inducing an immune response
which type of vaccine have the best result ?
living vaccines have the best result the resulting immunity lasting decades
when does hypersensitivity reaction occur during vaccines ?
HYPERSENSTIVITY REACTIONS NEVER OCCUR THE FIRST TIME - when an allergen meet the immune system
in can occur the 2nf and third time administrating the SAME vaccine
what is a monovalent vaccine
vaccine against one organism
what is a polyvalent vaccine
vaccine against several organisms such as MMR , DTPa
what are the characteristics of a good vaccine
ability to ellicit an appropriate immune response
long term protection
safe - vaccine itself should not cause a disease
stabe - retain the immunogenicitydespite storage
inexpensive
what are the potential safety hazard in live attenuated vaccine ?
polio - revision to wild type especially type 2 and 3
BCG and measles - severe disease in immunodeficient
varicella rooster - persistant infection
measles - hypersensitivity
mutations of the virus
storage
what are the potential safety hazards in killed organisms ? and drawbacks
polio - not killed
contamination with animal viruses
pretusisi - contamination with endotoxin
weaker immune response so need boosters
what are some diseases where no viruses are present ?
HIV
hepres
adenovirus
rhinovirus
chalmydia
most fungi
staphylococci
group A strep
syphillus
candida
malaria
what are some of the drawbacks for subunit vaccines
identifying specific antigen takes time
in any live attenuated vaccines how many weeks should we atleast wait until the next vaccination can be administered ?
at-least 4 weeks
why do we need to wait 4 weeks until we give the next administration ?
the immune system needs to kill all the organism before more is injected which can cause an outbreak of the disease
live vaccinations are given through which route ?
subcutaneous
killed inactivated vaccines are given through which route ?
intramuscularly
certain vaccination are not given before the 11th month such as and why ?
MMR
because the maternal IgG in the child fights against it and therefore no immune reaction and no memory b cells and the vaccination is void