save my exams vaccines ,diseases and monoclonal antibodies Flashcards
effectivenemess of vaccines
Highly effective with one vaccination giving a lifetime’s protection (although less effective ones will require booster / subsequent injections)
Generally harmless as they do not cause the disease they protect against because the pathogen is killed by the primary immune response
problems with vaccines
poor responses
antigenic variation
antigenic concleament
poor responses to vaccines
People can have a poor response (eg. they are malnourished and cannot produce the antibodies – proteins or their immune system may be defective)
antigenic variation
the variation (due to major changes) in the antigens of pathogens causes the vaccines to not trigger an immune response or diseases caused by eukaryotes (eg. malaria) have too many antigens on their cell surface membranes making it difficult to produce vaccines that would prompt the immune system quickly enough
antigenic concealment
this occurs when the pathogen ‘hides’ from the immune system by living inside cells or when the pathogen coats their bodies in host proteins or by parasitising immune cells such as macrophages and T cells (eg. HIV) or by remaining in parts of the body that are difficult for vaccines to reach
live attenuated vaccines
vweakened pathogens multiply slowly allowing for the body to recognise the antigens and trigger the primary immune response (plasma cells to produce antibodies)
These vaccines tend to produce a stronger and longer-lasting immune response
They can be unsuitable for people with weak immune systems as the pathogen may divide before sufficient antibodies can be produced
An example of this type of vaccine is the MMR (Measles, Mumps and Rubella)
herd immmunity
when a sufficiently large proportion of the population has been vaccinated (and are therefore immune) which makes it difficult for a pathogen to spread within that population
allows for the individuals who are unable to be vaccinated (e.g. children and those with weak immune systems) to be protected from the disease
active immunity
antibodies produced by the body
1-2 weeks before appears in blood
memory cells present
natural -exposure to pathogen
artifical-vaccination
passive
antibodies not produced by body
immediately appear in blood
no memoery cells
antibodied from another organism eg.breastmilk
artifical-manufactured and injected or transfered into organism
transmssion of hiv
sexual intercourse
blood donation
sharing of needles used by intravenous drug users
from mother to child across the placenta
mixing of blood between mother and child during birth
from mother to child through breast milk
strucutre of hiv
Two RNA strands
Proteins
A protein coat
A viral envelope consisting of a lipid bilayer and glycoproteins
Attachment proteins
replicaion of hiv
1)hiv attaches to receptors on lymphocyte
2)hiv injects its genetic material into the lymphocytes which becomes a host cell
3)viral rna enters the cell ,reverse transcriptase to produce a dna copy of viral rna
4)inserted into chromosome
5)genetic material into lymphocyte which which becomes a host cell
6)after making many copies of itself the host cell is destroyed by hiv
7)hiv infection leads to decreased lymphocytes numbers and reduced ability to produce antibbodies
symptoms of aids
mild flu-like symptoms
infected people might not know they are infected
gradually destroy and reduce the number of helper T cells present in a host
problems of aids
When an individual can no longer produce antibodies they are said to have advanced acquired immunodeficiency syndrome (AIDS)
As they can no longer produce antibodies against pathogens they are immuno-comprised and unable to fight off infections
They begin to suffer from diseases that would usually cause very minor issues in healthy individuals
These diseases are described as opportunistic
Tuberculosis (TB) is a common example
what happens to t cells if aids didnt exist
T cells play an important role in the specific immune response
They stimulate B cells, the production of antibodies and increased rates of phagocytosis