Cell recognition and the immune system Flashcards

1
Q

Describe how the immune system identifies its own cells

A

Each type of cell has specific molecules (proteins) on it cell surface. On its own cells these are self antigens which the immune system doesn’t make antibodies.

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2
Q

How do pathogens trigger the immune system?

A

The non-self antigens on its cell surface membrane will trigger the productions of antibodies

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3
Q

What type of cells does the immune system identify?

A

-Pathogens
-cells from other organisms of the same species
-abnormal body cells
-cancer cells

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4
Q

Define antigen

A

A protein molecule found on the cell surface membrane of cells that stimulates an immune response.

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5
Q

What is antigen variability

A

the ability of pathogens to change their surface antigens ( normally through a mutation in their genetic material)

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6
Q

What is the effect of antigen variability on disease prevention (vaccines)

A

Vaccine becomes ineffective as the new antigens are no longer recognised by the immune system which means it doesn’t produce the antigens to destroy the pathogen.

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7
Q

Explain phagocytosis (steps)

A

-Pathogen with antigens on its surface
-Phagocyte is attracted to pathogen through its receptors on its surface and attaches to the antigens
-Phagocyte engulfs the pathogen forming a phagosome
-Lysosome fuses with the phagosome and releases a lysozome enzyme which hydrolyses the pathogen
-The product of the hydrolysis are absorbed by the pathogen.

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8
Q

Describe T lymphocytes response to a foreign antigen (steps)

A

-phagocytosis
-Phagocyte presents the antigens onto its cell surface membrane (APC)
-Specific receptors on the helper T cells attach to the antigen
-This activates the helper T cell to divide by mitosis to form clones.
-Some of these clones differentiate into memory cells which stay in the blood and allow a quicker response if re-infected with the same pathogen.
-Some remain as helper T cells and activate phagocytosis, activate cytotoxic T cells and stimulate B cells to divide.

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9
Q

Describe the response of B lymphocytes to a foreign antigen (steps)

A

-Antigen of pathogen are taken up by the B cell and presented onto its cell surface membrane
-Helper T cell is binds to the antigens and activates the B cell (clonal selection)
-The activated B cell then divides by mitosis to form clones (clonal expansion)
-Some differentiate into memory B cells which remain in the blood and can differentiate into plasma cells if re-infected with the same pathogen.
-Some differentiate into plasma cells which produce the specific antibodies for (/complementary to) the antigen.

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10
Q

What defence mechanism is slower

A

specific

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11
Q

what defence mechanism is immediate

A

non-specific

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12
Q

Give examples of non-specific defence mechanisms

A

-physical barrier (skin)
-Phagocytosis

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13
Q

Give examples of specific defence mechanisms

A

-Cell mediated immunity
-Humoral immunity

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14
Q

T lymphocytes

A

-Type of white blood cell
made in bone marrow
-mature in thymus gland
-involved in cell mediated immunity

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15
Q

B lymphocyte

A

-type of white blood cell
-made and matures in bone marrow
-involved in humoral immunity

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16
Q

What are the differences between humoral response and cell mediated immunity

A

-cell mediated immunity involved T cells, whereas humoral response mainly involves B cells
-Cell mediated immunity doesn’t produce antibodies but humoral response does
-Cell mediated immunity is the first stage of the immune response whereas humoral response is the second stage.
-Cell mediated immunity is effective through cells, whereas humoral response is effective through body fluids

17
Q

Define antibody

A

-A protein with receptors that have a complementary shape to bind to a specific antigen

18
Q

Describe the structure of an antibody

A

-quaternary structure
-has disulphide bridges, variable region, antigen binding sites and short and long chains

19
Q

What is the role of the disulphide bridges in an antibody

A

To hold/join together the 4 polypeptide chains

20
Q

Why is the primary immune response slower

A

time taken for antigen presentation, clonal selection, clonal expansion and differentiation of B cells into plasma cells and then the production of antibodies is slower as there are no memory cells

21
Q

Why is the secondary immune response faster

A

The memory cells allow clonal expansion of the correct B cell to happen quickly which allows faster differentiation into plasma cells which secrete more antibodies faster.

22
Q

How do antibodies destroy pathogens?

A

-An antigen-antibody complex is formed
-Antigen binding site on the antibody is specific and will only bind to the antigen with the complementary shape
-Agglutination (clumps of bacterial cells form)
-Acts as markers for phagocytes to engulf them

23
Q

Define a vaccine

A

Contains antigens from the pathogen and stimulates the production of antibodies and memory cells against the target pathogen without causing the disease

24
Q

How do vaccines prevent a person from developing a certain disease

A

-produces a primary immune response
-memory B cells are made
-Exposure to the pathogen means memory cells differentiate into plasma cells faster so the antigens are made more quickly and in large numbers before symptoms can occur

25
Q

Define herd immunity

A

A form of immunity that occurs when the vaccination of a significant portion of the population provides a measure of protection for individuals who have not developed immunity
makes it less likely to spread

26
Q

What is active immunity

A

The individual produces their own antibodies as they have had direct contact with the pathogen

27
Q

What is passive immunity

A

The individual receives antibodies

28
Q

What is the difference between natural and artificial active immunity

A

natural active immunity is when a person has become infected by the disease, artificial is through the basis of immunization/ vaccines

29
Q

What is the difference between natural and active passive immunity

A

Natural is where the antibodies pass across placenta for fetus or breast milk for babies, artificial is where ready made antibodies are given to a person

30
Q

What are the differences between active immunity and passive immunity
-Memory B cells
-Antibodies outside source
-Long term/short term
-takes time/fast acting

A

-Active immunity involves memory B cells, passive immunity doesn’t
-Active immunity is where the antibodies are not introduced by outside source, passive immunity they are
-Active immunity is long term, passive immunity is not
Active immunity takes time to develop, passive immunity is fast acting

31
Q

What does HIV stand for

A

Human immunodeficiency virus

32
Q

What is the structure of HIV

A

-Genetic material (RNA)
-attachment protein (allows attachment to the receptor of the host cell/ helper T cell
-Lipid envelope (phospholipid bilayer)
-Capsid (encloses the enzyme and the 2 strands of RNA)
- reverse transcriptase enzyme

33
Q

What cells does HIV infect and destroy

A

Helper T cells

34
Q

Describe how HIV is replicated

A

-Attachment proteins attach to receptor molecules on the cell membrane of the helper T cell
-The capsid is released into the cell, where it un-coats and releases the genetic material (RNA) into the cell cytoplasm
-Inside the cell, reverse transcriptase enzyme is used to make complementary strand of DNA from the viral RNA template
-Double strand DNA is made and inserted into the human DNA
-Host cell enzyme are used to make viral proteins from the viral DNA ( found within the human DNA)
-The viral proteins are assumed into new viruses bud from the cell