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Prevention and control strategy (3)
host prevention
Immunity via immunization
behavioral change
improvement in general health (nutrition + exercise)
treatment (contacts + carriers)
Environmental control
personal hygiene
food protection
water supplies
sanitation and regulation
vector control
mosquitos and insecticides
animal pop control
passive immunization
transfer of ab from those who are immune
short
immediate protection
ex. maternal ab (natural) or HBIG (artificially acquired)
Active immunity
Vaccines
req for a good vaccine (6)
produce good humoral, cellular, and or local immune response similar to natural infection
produce protection against clinical disease and reinfection
give protection for years - lifetime
result in minimal side reactions or mild disese w/o delayed effects
simple administration
cost/benefit > cost/risk of natural disease & adverse risks of immunizations
Types of licensed vaccines
live/attenuated
killed
toxoids
conjugate
active components
purified
subunit
recombinant
viral vector, attenuated, recombinant
nucleic acid
Live-attenuated vaccines
live bacteria or viruses that infect but don’t cause disease
ex. MMR and Oral Polio
Killed whole vaccines
inactivated cells or viruses (can’t mult, infect, or cause disease)
ex. Injected polio and Hepatitis A
Toxoid
inactivated bacteria toxin (small molecule or protein)
ex. Tetanus and Diphtheria
Conjugate vaccines
subunit Ag conjugated to an unrelated protein
ex. hemophilus influenzae and staph aureus
what is the advantage of using conjugate vaccines?
B cell process vaccine and present protein Ag to Th
convert a TI vaccine to TD vaccine
much more effective for polysaccharide Ag
Subunit vaccines
immunogenic protein or other Ag only
ex. acellular pertussis and purified HBsAg for Hep B
Pros and cons for subunit vaccines
Pros
can’t cause the disease
can’t eliminate endotoxin or undesirable components
Cons
similar to killed-whole
purification can be expensive & difficult
a single Ag may not be effective as whole organism
Recombinant vaccines
subunit vaccine produced by genetic engineering
purification can be cheaper and easier
can use genes from viruses that can can’t be cultured
ex. HBsAg for Hep B
Engineered live-attenuated vaccines
“vector” virus altered to carry Ag from another pathogen
ex. SARS-CoV-2 and VSV for EbolaV
Pros and cons of Engineered live-attenuated vaccines
Pros
similar to live attenuated
greatly reduced change of causing disease
much easier to obtain usable live virus
Disadvantage
live genetically engineered organisms face regulation issues
could be difficult to engineer for proper expression
Ag protein may not also target to correct issue
Vaccinia can cause rare but severe illness
Nucleic acids (DNA or RNA) vaccines
genetically engineered DNA (as a plasmid) or RNA (as mRNA) which cells uptake and transform into a protein
ex. SARS-CoV-2
Pros and cons of Nucleic acids (DNA or RNA) vaccines
Pros
can induce CMI as well as humoral immunity
could use any gene standardization process
faster, easier, cheaper, more stable than traditional subunit vaccine
Cons
delivery methods must be worked out
regulatory issues
concern about auto-immunity (anti-DNA Ab) or integration to host DNA
What is considered a new era of vaccinology?
mRNA vaccine
Vaccine Adjuvants
substance that acts to accelerate, prolong, or enhance antigen-specific immune response when used as part of vaccine formulation
most activate early innate immunity
Characteristics affecting immune response
Administration
immunomodulator
route (oral, injection, etc)
injection site and needle size
dose and schedule
Host
age
weight
genetics
smoking status
nutrition and immune status
interference by other infections or maternal ab
barriers to immunization
cost of vaccine/insurance policies
disease risk perception
vaccine risk perception
religious/philosophical objections
complexity of schedule
missed opportunities
follow up difficulties
hard to reach populations
cold chain req
Vaccine concerns and hesitancy issues
safety
autism
overwhelming the immune sys
natural immunity superior
disease don’t exist anymore
big pharma conspiracy
individual rights vs ph needs
Key challenges (4)
limited resources
competitive health priorities
poor management
inadequate monitoring/supervision