Introduction to vaccination L28 Flashcards
(24 cards)
brief history of vaccines
first scientifically discovered by Edward Jenner in 1796 for small pox
tested knowledge that mild cattle disease cowpox would protect against deadly human disease small pox after observation with milk maids
what is passive immunity
this is the transfer of antibodies from an immune to non-immune individual
immediate short term protection
not producing own antibodies so no memory cells are formed
can either be natural or artificial
natural passive immunity
artificial passive immunity examples
antibody therapy - anti-venom, monoclonal antibodies
post exposure prophylaxis
anti-sera and what it is used for
this is a serum that contains specific antibodies against a particular antigen
used to provide passive immunity, neutralise toxins, pathogens or venoms, and treat people exposed to disease
how is anti-sera made?
1) inject an animal or human (typically horse or sheep) with an antigen
2) animal/human produces antibodies as causes an immune response
3) blood is collected at certain intervals, purified and serum is extracted
applications of antibody transfers
rapid treatment during acute illness of patients like EBOLA, measles, rabies etc or for snake venom or toxins
or can be used as a preventative measure - yellow fever
advantages of antibody transfers
quick acting and immediate protection - useful for emergiencies - which is important for some cases such as being infected with snake venom, need fast response
passive immunisation can support a deficient immune system which is good for high risk individuals or immunocompromised
no need for prior exposure , protecting individuals without them having to encounter the disease
disadvantages of antibody transfers
antibody levels fall and protection fades within months - short term protection only as no memory cells produced
antibody treatments must be given via intravenous injection
can get serum sickness - especially with animal derived serums
antiseras are expensive and complicated to produce and store
monoclonal antibodies mAB
identical antibodies produced by a single B cell clone that all target one specific antigen epitope
how are monoclonal antibodies made?
- fuse a specific B cell with a cancer cell - hydridoma
- hybridoma produces larges amounts of one type of antibody
- antibodies are harvested and purified
how do monoclonal antibodies provide protection ?
neutralise pathogens and toxins by binding and blocking
triggers ADCC via Fc region
enhances phagocytosis
can be designed to target cancer cells, viruses, or inflammatory molecules
advantages of monoclonal antibodies
single specificity
near unlimited supply of antibodies
even antibodies with very rare specificities can be isolated
antibodies can be manipulated / customised
disadvantages of monoclonal antibodies
expensive to make
need IV infusion
can cause immune reaction
not long lasting
why do we humanise a mouse monoclonal antibody
to reduce immunogenicity - to avoid human immune system from attacking it
and to make them suitable for therapeutic use in humans
how to humanise a mouse monoclonal antibody
replace mouse antibody parts with human antibody sequences whilst keeping antigen binding sites CDRs intact
- isolate mouse Ab genes and identify the CDRs region
- graft mouse CDRs onto a human antibody framework
- modify any necessary changes
- express new humanised Ab in host cells
- test for function
modern ways of making monoclonal antibodies
directly from human B cells
phage display
EBV transformation
in vitro expansion and selection
what are the principles of vaccination
- to introduce the immune system to a pathogen in a controlled environment
- cause the immune system to remember the pathogen and respond to it
- enable immune system to effectively clear pathogen to prevent disease
the ideal vaccine properties
long lasting immunity
safe
stable in field conditions
easy to store and administer
single dose
affordable and accessible to all
pathogen evolution proof
live attenuated type of vaccine
these are vaccines made from weakened forms of pathogen that can replicate but do not cause disease in healthy individuals
ensures that it mimics natural infection, very long lasting immunity, required 1-2 doses and induces both humeral and cell mediated immunity
however risk in immunocompromised people, can revert back to virulent form and require cold storage
killed whole organism type of vaccine
vaccines made from inactivated pathogens that cannot replicate but still trigger immune response
safer for immunocompromised people, easier to store, induced mostly humeral immunity and may require boosters
however, weaker immune response than live attenuated, often need lots of doses
toxoid type of vaccie
toxin dervied from pathogen
subunit type of vaccine
bacteria and viruses, purified protein or polysaccharides from cell wall
doesnt use entire virus or bacteria, just the components of pathogenic organisms - the pathogenic agents
good as no extraneous pathogen particles like DNA
however, proteins may differ when not in situ and production can be expensive
vector vaccines
antigen genes inserted into the vaccinia virus genome with all virulent factors removed
example - Rabies virus G protein, hepatitis B surface antigen