Vaccinations Flashcards
(34 cards)
vaccination
Utilizes two key elements of the adaptive immune
response, Specificity and Memory
what do memory cells do
allow the immune system to mount a
much stronger response to a second encounter with
an Ag. Faster and more effective.
what do vaccines contain
altered forms of a pathogen or its toxins which retain antigenicity but are innocuous. • Subunit •Killed whole organism •Attenuated live •Recombinate •DNA
bacterin
killed bacteria, leptospirosis
live bacterial vaccines
strep
toxoid
Inactiviated bacterial toxin, e.g.
Clostridium tetani
antitoxins
horse or sheep derived serum
tetanus
attenuated or modified live
whole organism
category I USDA classification
Vaccines that contain inactivated
recombinant organisms or purified
antigens derived from recombinant
organisms.
category II USDA classification
Vaccines containing live organisms that
contain gene deletions or heterologous
maker genes.
category III USDA classification
Vaccines that contain live expression
vectors expressing heterologous genes for
immunizing antigens or other stimulants
category IV USDA classification
Other genetically engineered vaccines
such as polynuceotide vaccines.
category 1
•Gene cloning can be used to produce large quantities of antigen in culture. •Felv and Lyme disease vaccines •Results in pure protein antigen but may be inefficient
category 2
•Molecular genetic techniques make it possible to
modify genes of organisms so they become
irreversibly attenuated. (so they can not revert to
virulence and cause disease.)
•Pseudorabies vaccine in pigs an example.
category 3
• Genes coding for protein antigens can be cloned directly into a
variety of organisms. The recombinant organism itself can be used as
a vaccine.
• Use of Canarypox-vectored vaccine can over ride the blocking by
maternal antibodies
• FeLV, West Nile, Canine parvo/distemper, equine influenza, and
rabies.
category 4
•Another method of vaccination involves injection,
not of a protein antigen, but of DNA that encodes
foreign antigens.
CMI
cell mediated immunity
t-cells
humoral immunity
b-cells
anitbody
MLV vs killed in vaccines
•MLV and genetically engineered vaccines • Long-lasting immunity •Complete immunity – Tc cells and B-cells •CMI and Humoral immunity • Stimulate memory with a single dose • Some lifelong (genetically engineered vaccines) •Require fewer revaccinations •Increase reaction issues •Revert to virulence
killed vaccines
• Short – lived systemic immunity • 2-4 months some longer 1-2 years • Stimulate primary B-cell => Ab (humoral immunity) but no CMI (T-cell) •Require multiple doses •Booster 2-6 weeks after 1st dose •May require annual revaccination throughout animal’s life •Revaccination = key to immunologic memory •Adjuvant – stimulate greater response •May cause adverse reactions •Injection site granulomas
safety of MLV
•Can induce disease (reversion to virulence)
•May cause abortion
•Depressed T-cell function in pregnant
animals
•Reason for development of gene vaccines.
safety of killed vaccines
- Does not cause disease
* Safe in pregnant animals
safety of live bacterial vaccines
- Can cause disease in humans
* Can cause abscesses without good technique
passive immunity
•Results from the transfer of Antibodies from one
individual to another
• Parenteral administration (hyperimmune serums or
antitoxins)
• Oral administration of monoclonal Ab
• Ingestion of Abs in colostrum by the neonate
• Plasma transfusion
• Level and duration of passive immunity is largely
dependent upon the amount of antibodies taken in
•Passive immunity is immediate where Abs are
administered IV/IM; Oral = 2-3 hours.