Immunology Flashcards
(17 cards)
Use the data in the table above and your knowledge of the immune response to suggesr why HIV controllers do not develop symptoms of AIDS
- HIV controllers have more CD4 cells
- And a lower viral load to infect T cells
- So there is more activation of B cells, cytotoxic T cells and phagocytes
- With more B cells, more plasma and more antibodies being produced
- Body is able to destroy other microbes/pathogens someone who suffers from AIDS wouldn’t be able to
Describe how HIV is replicated
- Attachment proteins on HIV attach to receptors on T cell.
- RNA enters T cell
- Reverse transcriptase changes viral RNA to viral DNA
- Viral protein, capsid and enzymes produced
- Virus assembled and released from cell.
Describe how the human immunodeficiency virus is replicated once inside helper t cells
- RNA converted into DNA using reverse transcriptase
- DNA incorporated into helper t cell DNA
- DNA transcribed into HIV mRNA
- HIV mRNA translated into new HIV/viral proteins for assembly into viral particles
Describe how a phagocyte destroys a pathogen present in the blood
Engulfs
Forming phagosome and fuses with lysosome
Lysozymes hydrolyze
Determining the genome of the viruses could allow scientists to develop a vaccine
Explain how
Scientists could identify proteins
They could then identify potential antigens
What is a monoclonal antibody
Antibodies with the same tertiary structure
OR
An antibody produced from identical/ cloned plasma cell/ B cells
Describe and explain the role of antibodies in stimulating phagocytosis
Antibodies bind to antigens and are markers
They cause clumping and agglutination which attracts phagocytes
During vaccination, each animal is initially injected with a small volume of Venom. 2 weeks later it is injected with a larger volume of Venom.
Use your knowledge of the humoral immune response to explain this vaccination program
- B Cell specific to the Venom reproduced by mitosis
- B Cells produce plasma cells in memory cells
- The second dose produces antibodies in secondary immune response in higher concentrations and more quickly
In the UK, children are vaccinated against NM. Describe how vaccination can lead to protection against NM
- Antigen on surface of NM binds the surface protein on a B cell
- B. Cell divides by mitosis
- Stimulated by t cells
- B. Cells/ plasma cells release antibodies
- B cells become memory cells
- Memory cells produce plasma/ antibodies faster
When a vaccine is given to a person, it leads to the production of antibodies against a disease causing organism. Describe how
- Vaccine contains antigen from pathogen
- Body cell presents antigen on its surface
- T cell with complementary receptor protein binds to antigen
- T. Cell stimulates B. Cell
- With complementary antibody on its surface
- B. Cell secretes large amounts of antibody
- B. Cell device to form clone or secreting/producing the same antibody
Explain why the number of hiv particles in the blood rises during the first few months after infection
- hiv is invading cells which make new viruses
2. Cells release viruses into blood a
Describe how antibodies are produced in the body following a viral infection
- virus contains antigen;
- virus engulfed by phagocyte
- presents antigen to B-cell
- memory cells / B-cell becomes activated;
- (divides to) form clones
- by mitosis;
- plasma cells produce antibodies;
- antibodies specific to antigen;
- correct reference to T-cells / cytokines
AZT inhibits the enzyme that synthesises DNA from HIV RNA. explain why it does not destroy HIV in the body but stops or slows the development of AIDS
- Person (infected with HIV) has HIV DNA (in
their DNA); - New HIV (particles) still made;
- (AZT) inhibits reverse transcriptase;
- (AZT) stops these (new HIV particles) from
forming new HIV DNA;
OR
Slows / stops replication of HIV; - Stops destruction of more / newly infected
T cells; - So immune system continues to work (and
AIDS does not develop);
Explain why viruses are described as acellular and non living
Acellular - no cell surface membrane
Non living- cannot reproduce on its own
Give one reason why antibiotics are not effective against viruses
Do not have bacterial structures/enzymes
OR
Do not have metabolic processes
OR
Do not have a cell wall/murein;
Explain how the use of antibiotics has led to antibiotic-resistant strains of bacteria becoming a common cause of infection acquired when in hospital
- (Some bacteria have) alleles
for resistance; - (Exposure to) antibiotics is the
selection pressure
OR
Non-resistant bacteria die
OR
Resistant bacteria
survive/reproduce; - More antibiotics used in
hospital (compared with
elsewhere)
OR
Patients have weakened
immune systems
OR
(So) high frequency of
resistance allele (in bacterial
population);
Suggest and explain one reason why bacteria resistant to tetracycline are more common than bacteria resistant to streptomycin in these farm animals
(Context is not necessary)
- Tetracycline used more often / in higher doses;
- Resistant bacteria more likely to (survive and
reproduce and) pass on allele/gene for
(tetracycline) resistance;
OR
- More / higher frequency of mutations (for
tetracycline resistance); - (so) gene passed on to more bacteria;
OR
- Tetracycline used over longer time period;
- More time for (chance) mutation to occur / for
selection to occur;