Immunology Flashcards

(17 cards)

1
Q

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

A
  • 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
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2
Q

Describe how HIV is replicated

A
  • 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.
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3
Q

Describe how the human immunodeficiency virus is replicated once inside helper t cells

A
  • 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
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4
Q

Describe how a phagocyte destroys a pathogen present in the blood

A

Engulfs
Forming phagosome and fuses with lysosome
Lysozymes hydrolyze

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5
Q

Determining the genome of the viruses could allow scientists to develop a vaccine
Explain how

A

Scientists could identify proteins
They could then identify potential antigens

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6
Q

What is a monoclonal antibody

A

Antibodies with the same tertiary structure

OR

An antibody produced from identical/ cloned plasma cell/ B cells

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7
Q

Describe and explain the role of antibodies in stimulating phagocytosis

A

Antibodies bind to antigens and are markers
They cause clumping and agglutination which attracts phagocytes

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8
Q

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

A
  • 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
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9
Q

In the UK, children are vaccinated against NM. Describe how vaccination can lead to protection against NM

A
  • 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
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10
Q

When a vaccine is given to a person, it leads to the production of antibodies against a disease causing organism. Describe how

A
  • 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
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11
Q

Explain why the number of hiv particles in the blood rises during the first few months after infection

A
  • hiv is invading cells which make new viruses
    2. Cells release viruses into blood a
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12
Q

Describe how antibodies are produced in the body following a viral infection

A
  1. virus contains antigen;
  2. virus engulfed by phagocyte
  3. presents antigen to B-cell
  4. memory cells / B-cell becomes activated;
  5. (divides to) form clones
  6. by mitosis;
  7. plasma cells produce antibodies;
  8. antibodies specific to antigen;
  9. correct reference to T-cells / cytokines
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13
Q

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

A
  1. Person (infected with HIV) has HIV DNA (in
    their DNA);
  2. New HIV (particles) still made;
  3. (AZT) inhibits reverse transcriptase;
  4. (AZT) stops these (new HIV particles) from
    forming new HIV DNA;
    OR
    Slows / stops replication of HIV;
  5. Stops destruction of more / newly infected
    T cells;
  6. So immune system continues to work (and
    AIDS does not develop);
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14
Q

Explain why viruses are described as acellular and non living

A

Acellular - no cell surface membrane
Non living- cannot reproduce on its own

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15
Q

Give one reason why antibiotics are not effective against viruses

A

Do not have bacterial structures/enzymes
OR
Do not have metabolic processes
OR
Do not have a cell wall/murein;

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16
Q

Explain how the use of antibiotics has led to antibiotic-resistant strains of bacteria becoming a common cause of infection acquired when in hospital

A
  1. (Some bacteria have) alleles
    for resistance;
  2. (Exposure to) antibiotics is the
    selection pressure
    OR
    Non-resistant bacteria die
    OR
    Resistant bacteria
    survive/reproduce;
  3. More antibiotics used in
    hospital (compared with
    elsewhere)
    OR
    Patients have weakened
    immune systems
    OR
    (So) high frequency of
    resistance allele (in bacterial
    population);
17
Q

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)

A
  1. Tetracycline used more often / in higher doses;
  2. Resistant bacteria more likely to (survive and
    reproduce and) pass on allele/gene for
    (tetracycline) resistance;

OR

  1. More / higher frequency of mutations (for
    tetracycline resistance);
  2. (so) gene passed on to more bacteria;

OR

  1. Tetracycline used over longer time period;
  2. More time for (chance) mutation to occur / for
    selection to occur;