5. Cell Recognition and immune system Flashcards

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1
Q

How does the body detect pathogens?

A

Body can recognise ‘non self’ protiens on the set face of the cell

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2
Q

What is an antigen

A

(Macromolecule) markers that allow cell to cell recognition. Can either be self or non self

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3
Q

How do pathogens avoid causing a specific immune response?

A

Antigen variability, antigen change due to genetic mutations.
Memory cells can no longer bind

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4
Q

How does passive immunity happen?

A

Anti-venoms, fetal immunity (breast milk)

No memory cells are made, immunity is temporary

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5
Q

What is (natural) active immunity?

A

Organism is infected, triggering numeral immune response

Antibodies made but symptoms of disease may be displayed

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6
Q

What is (artificial) active immunity?

A

Vaccination, body produces antibodies and memory cells providing long-term immunity

Without experiencing symptoms

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7
Q

Describe process of phagocytosis

A
  • phagocyte is attracted to pathogen by the pathogens chemical products
  • pathogen attaches to receptors on phagocyte
  • lysosomes migrate to forming phagosome as pathogen gets engulfed
  • lysosomes release lysoZYmes into phagosome, these hydrolyse the pathogen
  • pathogen absorbs hydrolysis products

[ext] phagocyte ‘present’ pathogens antigens. (Not part of cell phagocytosis)

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8
Q

What are the two types of phagocytes?

A

Neutrophils
Macrophages

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9
Q

Two examples of specific immune responses?

A

Cell mediated- T cells
(matured in thymus)

Humeral- B cells
(matured in bone marrow)

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10
Q

Summarise the role of T cells in CELL-MEDIATED immunity

A
  • receptors helper T-cell fit onto antigen presenting cell
  • T-cell is activated to divide by mitosis
  • cloned T cells can either:
    Become memory cell
    Stimulate phagocytosis
    Stimulate B cell
    Activate TC cell
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11
Q

What is a TC cell?
Explain how they carry out function.

A

Cells that kill infected body cells by releasing the protein perforin. This protein makes holes in membrane

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12
Q

When are b cell produced produced?

A

At birth, around 10 million of each are present in body.

B cells are not produced in response to pathogen, they only multiply in response to pathogen

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13
Q

When b cells are cloned they can either be…

A

plasma cells or memory cell.

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14
Q

What cells are involved in primary and secondary responses

A

Primary - PRODUCTION of antibodies and memory cells

Secondary - memory cells recognise pathogen, providing faster response on later infection

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15
Q

How are monoclonal antibodies used to treat cancer? (indirect and direct)

A

DIRECT
Antibodies specific to cancer antigen blocks chemicals that stimulate uncontrolled growth.

INDIRECT
Radioactive or cytotoxic material is attached to MA, binding to and killing cancer

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16
Q

How are monoclonal antibodies used in diagnosis

A

Eg. Prostate cancer causes an increase in PSA antibodies, this is detected and causes concern for further testing

The ELISA test

17
Q

Give three reasons why monoclonal antibodies raise ethical issues

A

Mice involved in production

Deaths linked with MA

drug testing (2006 six volunteers had multiple organ failure)

18
Q

What 5 things are necessary for an effective vaccination program

A

Economically viable

Few side effects

Viable transport, storage + production

Training of staff to perform vaccination

Majority of population must be vaccinated = herd immunity

19
Q

6 reasons why vaccination might not work

A

-will not work on people with defected immune systems

  • disease may develop immediately after vaccination, potentially spreading to others

-antigen variability
-variants of the same pathogen

-Some pathogens ‘hide’ in body cells eg HIV

-some may object because of medical or ethical issues

20
Q

Discuss ethical issues of vaccination

A

Testing often involves animals

Potentially long lasting side effects

Risks involved in human testing

Should it be compulsory so herd immunity can be achieved?

21
Q

What do Plasma cells do?

A

Secrete antibodies into blood plasma. Survive for short amount of time but produce a lot of antibodies

22
Q

What do memory cells do?

A

Memory cells live longer, when they ‘recognise’ the same pathogen they divide rapidly and develop into plasma cells.
They provide readiness for future infections

23
Q

Summarize the humoral response.

A

B-cell takes up antigens of pathogens and presents them.

Helper T cells attach, activating B cell.

Stimulated to clone into plasma or memory cells.

24
Q

Draw and label an antibody

A

go online for images;
- light chain
- heavy chain
- constant region
- variable region
- antigen binding sites

25
Q

Explain how antigens are destroyed by antibodies.

A
  • agglutination of bacterial cells, clumps of cells are formed (antigens have multiple binding sites) Easier for phagocytes to find.
  • act as markers for phagocytes to engulf cells they are attached
26
Q

Where do T and B cells mature?

A

T cells, mature in thymus

B cells, mature in bone marrow

27
Q

Explain how vaccinations work.

A
  • Small amounts of weakened/ dead pathogen injected
  • B cells are activated (plasma/memory)
  • memory cells remain in the bloodstream
28
Q

Explain the concept of herd immunity

A

If enough of the population is vaccinated, pathogens cannot easily spread.

protects those who aren’t vaccinated/ can’t get vaccinated.

29
Q

Draw the structure of HIV.

A
  • RNA
  • Reverse transcriptase
  • capsid
  • matrix
  • attachment proteins
  • membrane
30
Q

Summarize the replication of HIV

A

HIV is transported in blood until it attaches to a CD4 PROTEIN on a helper T-cell

HIV capsule fuses with the Th-cell, RNA and reverse transcriptase enter.

Th-cell synthesises new viral enzymes and RNA

31
Q

How do new viral RNA and proteins exit host cell? (HIV)

A

Move to cell membrane, and is released, New HIV molecules membrane is from Th-cell

32
Q

What is AIDS?

A

Replication of viruses via Th-cells interferes with immune response. The host is vulnerable to infections and cancer.

33
Q

Explain the process of the Enzyme linked immunosorbent assay (ELISA)

7 steps…

A
  • add a test sample to the base of a beaker
  • wash to remove any unbound test sample
  • add an antibody, complementary in shape of antigen that is being tested for
  • wash any unbound antibody
  • add a second antibody antibody that is complementary to the first, enzyme attached to it, rinse unbound antibodies
  • add substrate for enzyme - colorless in absence of enzyme, coloured in the presence of enzyme
  • colour indicates presence of enzyme and therefore antigen. intensity indicates quantity present
34
Q

Why are antibodies ineffective against viruses?

A

viruses rely on host cells for metabolic pathways. no mechanisms for antibodies to disrupt.
inside organisms own cells, cant be reached

35
Q
A