Cell Recognition and the Immune System Flashcards

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1
Q

What is the non-specific immune response?

A

It is the immediate response to a pathogen and is the same for all pathogens. Includes phagocytosis.

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2
Q

What is the specific immune response?

A

It is the slower response to a pathogen and is the specific to each pathogens. Includes the cell response and the humoral response.

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3
Q

In what ways does your body try to prevent pathogens from invading?

A
  1. Lysozymes in tears and saliva breaks down pathogens.
  2. Mucus membranes on respiratory and reproductive systems
  3. Acid in the stomach
  4. Skin
  5. Immune system
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4
Q

How do phagocytes engulf and destroy pathogens?

A
  1. Phagocyte engulfs pathogen in endocytosis
  2. Pathogen is put in a vesicle
  3. Lysosomes containing digestive enzymes (lysozymes) fuse with vesicle
  4. Pathogen is hydrolysed and digested
  5. Waste is released via exocytosis and the pathogens antigen is presented on the phagocytes cell membrane
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5
Q

What is cell mediated immunity?

A

T-lymphocytes respond to an organisms own cells that have been invaded by external material e.g. a virus.

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6
Q

How do T-lymphocytes tell invader cells apart from normal cells?

A

A pathogens antigens are presented on the phagocyte cell surface and T-lymphocytes have protein receptors on their surface that are complimentary to the antigen.

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7
Q

What do T-helper cells do?

A

They activate B cells and make memory cells.

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8
Q

What do T-cytotoxic cells do?

A

They release chemicals that kill infected body cells by damaging cell membranes.

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9
Q

How do cytotoxic T cells destroy infected cells?

A

They produce a protein that makes holes on the cell surface membrane of the infected cell, making the membrane freely permeable, which is very effective against viruses.

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10
Q

What are B cells?

A

They are a type of white blood cell covered with antibodies. These bind to antigens to form antigen-antibody complexes.

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11
Q

What happens when B cells are activated?

A

They produce plasma B cells by mitosis, which are identical clones of the B cell. These secrete antibodies that are specific to the antigens. These are called monoclonal antibodies.

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12
Q

What do monoclonal antibodies do?

A

They bind to the antigens on the surface of the pathogen, forming antigen-antibody complexes. They have two binding sites so can bind to two antigens at once and clump them together. This is called agglutination. These clumps are them engulfed by phagocytes.

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13
Q

What is agglutination?

A

When antibodies binds to antigens, clumping them up with their two binding sites.

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14
Q

Describe the cell mediated response. (4)

A
  • Bind to antigen presenting cells
  • Divide by mitosis
  • T helper cells produce chemicals which cause B lymphocytes to divide in mitosis
  • T cytotoxic cells produce chemicals that kill pathogens or infected cells
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15
Q

Describe the humoral response (4)

A
  • T helper cells produce chemicals to aid mitosis in B cell activation
  • Memory cells are made for future infections
  • Plasma cells are made to make antibodies
  • Antibodies bind to pathogens
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16
Q

What is the structure of an antibody?

A
  • They are proteins made of chains of amino acids.
  • Their specificity depends on their variable region.
  • Each antibody has a unique variable region due to its tertiary structure, making them complimentary to one type of antigen only.
  • All antibodies have the same constant region
17
Q

Describe how phagocytosis of a virus leads to presentation of its antigens

A
  1. Phagosome/vesicle fuses with lysosome
  2. (Virus) destroyed by lysozymes/hydrolytic enzymes
  3. Peptides/antigen (from virus) are displayed on the cell membrane;
18
Q

Describe how presentation of a virus antigen leads to the secretion of an antibody against this virus antigen.

A
  1. Helper T cell/TH cell binds to the antigen (on the antigen-presenting cell/phagocyte)
  2. This helper T/TH cell stimulates a specific B cell
  3. B cell clones OR B cell divides by mitosis 4. (Forms) plasma cells that release antibodies;
19
Q

Some white blood cells are phagocytic. Describe how these phagocytic white blood cells destroy bacteria.

A

1.Phagocyte attracted to bacteria by chemicals / recognise antigens on bacteria asforeign
2. Engulf / ingest bacteria
3. Bacteria in vacuole / vesicle
4. Lysosome fuses with / empties enzymes into vacuole
5. Bacteria digested / hydrolysed;

20
Q

Vaccines protect people against disease. Explain how.

A
  1. Vaccines contain antigens / dead / weakened pathogens / antigens dead / weakened pathogens are injected
  2. Memory cells made
  3. On second exposure memory cells produce antibodies
  4. Idea of memory cells responding
  5. Rapidly produce antibodies / produces more antibodies.
  6. Antibodies destroy pathogens;
21
Q

HIV can only infect cells that express the CD4 cell-surface receptor, such as T-cells. Explain why.

A

The attachment protein on the virus have a specific tertiary structure which allows them to bind to the complementary CD4 receptor but not any other receptors.

22
Q

Phagocytes and lysosomes are involved in destroying microorganisms. Describe how. (3)

A
  1. (Phagocyte engulfs) to form vacuole / vesicle / phagosome;
    Accept surrounds bacteria with membrane
  2. Lysosome empties contents into vacuole / vesicle / phagosome;
    Accept joins / fuses
  3. (Releasing) enzymes that digest / hydrolyse bacteria;
    Ignore breakdown / destroy / lytic enzymes
23
Q

When a pathogen enters the body it may be destroyed by phagocytosis.
Describe how. (4)

A
  1. Phagocyte attracted by a substance / recognises (foreign) antigen;
    Accept named substance eg chemical / antigen
  2. (Pathogen)engulfed / ingested;
    Accept: description
  3. Enclosed in vacuole / vesicle / phagosome;
  4. (Vacuole) fuses / joins with lysosome;
  5. Lysosome contains enzymes;
    Accept named example of enzyme
  6. Pathogen digested / molecules hydrolysed;
    Neutral: Destroyed
24
Q

Describe the difference between active and passive immunity. (5)

A
  1. Active involves memory cells, passive does not;
  2. Active involves production of antibody by plasma cells / memory cells;
  3. Passive involves antibody introduced into body from outside / named source;
  4. Active long term, because antibody produced in response to antigen;
  5. Passive short term, because antibody (given) is broken down;
  6. Active (can) take time to develop / work, passive fast acting.
25
Q

Describe how B-lymphocytes respond when they are stimulated by antigens. (4)

A
  1. Divide by mitosis / form clones;
  2. Produce plasma cells; (plasma cells)
  3. Make antibodies;
  4. (Plasma cells) produce memory cells;
26
Q

When a vaccine is given to a person, it leads to the production of antibodies against a disease-causing organism. Describe how. (5)

A
  1. Vaccine contains antigen from pathogen;
  2. Phagocyte presents antigen on its surface;
  3. T cell with complementary receptor protein binds to antigen;
  4. T cell stimulates B cell;
  5. (With) complementary antibody on its surface;
  6. B cell secretes large amounts of antibody;
  7. B cell divides to form clone all secreting / producing same antibody
27
Q

Bacterial meningitis is a potentially fatal disease affecting the membranes around the brain. Neisseria meningitidis (Nm) is a leading cause of bacterial meningitis.
In the UK, children are vaccinated against this disease. Describe how vaccination can lead to protection against bacterial meningitis. (5)

A
  1. Antigen on surface of N. meninigitidis / bacterium binds to surface protein / surface receptor on a T cell.
  2. (Activated) T cell divides by mitosis / produces clone;
  3. (Division) stimulated by cytokines / by B cells;
  4. B cells / plasma cells release antibodies;
  5. (Some) B cells become memory cells;
  6. Memory cells produce plasma / antibodies faster
28
Q

Describe how humans produce antibodies against a pathogen such as Salmonella. (6)

A
  1. Salmonella pathogen has specific antigen on surface;
  2. Salmonella pathogen engulfed by phagocyte;
  3. T-cells activate B-cells;
  4. B-cell with complementary/specific receptor antibody activated/
    clonal selection;
  5. B-cells divide/form clone/clonal expansion;
  6. Plasma cells make antibodies;
  7. Specific to antigen/bind to salmonella bacterial antigen;
    Accept macrophage presents antigen to T/B cells;
    Accept T-cells release factors;