2.4 T Lymphocytes and cell-mediated immunity & B lymphocytes and humoral immunity Flashcards

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1
Q

What is immunity?

A

The ability of organisms to resist infection by protecting against disease-causing microorganisms or their toxins that invade their bodies. It involves the recognition of foreign material (antigens)

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2
Q

What is an antigen?

A

• Any part of an organism or substance that is recognised as non-self by the immune system and stimulates an immune response.
• Antigens are usually glycoproteins, sometimes glycolipid or polysaccharide that are part of the cell surface membranes or cell walls of invading cells, such as microorganisms, or abnormal body cells, such as cancer cells.
• The presence of an antigen triggers the production of an antibody as part of the body’s defence system
• Immune system recognises as ‘self’ or ‘nonself’ = enables identification of cells from other organisms of same species, pathogens, toxins and abnormal body cells

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3
Q

What are B lymphocytes?

A
  • They mature in the bone marrow
  • They are associated with humoral immunity, that is, immunity involving antibodies that are present in body fluids, or ‘humour’ such as blood plasma
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4
Q

What are T lymphocytes?

A
  • They mature in the thymus gland
  • They are associated with cell-mediated immunity, that is immunity involving body cells
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5
Q

What are lymphocytes produced by?

A

Stem cells in the bone marrow

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6
Q

What are non-specific and specific responses?

A
  • Immune responses such as phagocytosis are non-specific and occur whatever the infection.
  • The body also has specific responses that react to specific antigens. These are slower in action at first, but they can provide long-term immunity. This depends on a type of white blood cell called a lymphocyte
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7
Q

How can T lymphocytes distinguish invader cells from normal cells?

A
  • Phagocytes that have engulfed and hydrolysed a pathogen present some of a pathogen’s antigens on their own cell-surface membranes
  • Body cells invaded by a virus present some of the viral antigens on their own cell-surface membrane
  • Transplanted cells from individuals of the same species have different antigens on their cell-surface membrane
  • Cancer cells are different from normal body cells and present antigens on their cell-surface membranes
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8
Q

What are antigen-presenting cells?

A

Cells that display foreign antigens on their surface because they can present antigens of other cells on their own cell-surface membrane

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9
Q

What is cell mediated immunity/cellular response?

A

T lymphocytes will only respond to antigens that are presented on a body cell, rather than to antigens within the body fluids

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10
Q

What is the role of the receptors on T cells?

A
  • The receptors on each T cell respond to a single antigen
  • It follows that there is a vast number of different types of T cell, each one responding to a different type of antigen
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11
Q

What are the stages in the response of T lymphocytes to infection by a pathogen?

A
  1. Pathogens invade body cells or are taken in by phagocytes
  2. The phagocyte places antigens from the pathogen on its cell-surface membrane
  3. Receptors on a specific helper T cell fit exactly onto these antigens
  4. This attachment activates the T cell to divide rapidly by mitosis and form a clone of genetically identical cells
  5. The cloned T cells:
    a. develop into memory cells that enable a rapid response to future infections by the same pathogen
    b. stimulate phagocytes to engulf pathogens by phagocytosis
    c. stimulate B cells to divide and secrete their antibody
    d. activate cytotoxic T cells
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12
Q

How do cytotoxic T cells kill infected cells?

A
  • Cytotoxic T cells kill abnormal cells and body cells that are infected by pathogens,
  • by producing a protein called perforin that makes holes in the cell-surface membrane.
  • These holes mean the cell membrane becomes freely permeable to all substances and the cell dies as a result.
  • This illustrates the vital importance of cell-surface membranes in maintaining the integrity of cells and hence their survival
  • The action of T cells is most effective against viruses because viruses replicate inside cells. As viruses use living cells in which to replicate, this sacrifice of body cells prevents viruses multiplying and infecting more cells.
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13
Q

What is the role of B cells in humoral immunity?

A
  1. The surface antigens of an invading pathogen are taken up by a B cell
  2. The B cell processes the antigens and presents them on its surface
  3. Helper T cells attach to the processed antigens on the B cell thereby activating the B cell
  4. The B cell is now activated to divide by mitosis to give a clone of plasma cells
  5. The cloned plasma cells produce and secrete the specific antibody that exactly fits the antigen on the pathogen’s surface
  6. The antibody attaches to antigens on the pathogen and destroys them
  7. Some B cells develop into memory cells. These can respond to future infections by the same pathogen by dividing rapidly and developing into plasma cells that produce antibodies. This is the secondary immune response
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14
Q

What is humoral immunity?

A

It involves antibodies which are soluble in the blood and tissue fluid of the body. There are many different types of B cell, possibly as many as 10 million, and each B cell starts to produce a specific antibody that responds to one specific antigen.

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15
Q

What is the response of B lymphocytes to a foreign antigen?

A

When an antigen, for example, a protein on the surface of a pathogen, foreign cells, toxin, damaged or abnormal cell, enters the blood or tissue fluid, there will be one B cell that has an antibody on its surface whose shape exactly fits the antigen, that is, they are complementary. The antibody therefore attaches to this complementary antigen. The antigen enters the B cell by endocytosis and gets presented on its surface.

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16
Q

What is clonal selection?

A

T cells bind to processed antigens and stimulate the B cell to divide by mitosis to form a clone of identical B cells, all of which produce the antibody that is specific to the foreign antigen. This is called clonal selection and accounts for the body’s ability to respond rapidly to any of a vast number of antigens

17
Q

How are monoclonal antibodies released?

A

A typical pathogen has many different proteins on its surface, all of which act as antigens. Some pathogens, such as the bacterium that causes cholera, also produce toxins. Each toxin molecule also acts as an antigen. Therefore many different B cells make clones, each of which produces its own type of antibody. As each clone produces one specific antibody these antibodies are referred to as monoclonal antibodies. In each clone, the cells produced develop into one of two types of cells.

18
Q

Describe plasma cells

A
  • Secrete antibodies usually into blood plasma
  • These cells survive for only a few days but each can make around 2000 antibodies every second during its brief lifespan
  • These antibodies lead to the destruction of the antigen
  • Plasma cells are responsible for the immediate defence of the body against infection
19
Q

What is primary immune response?

A

The production of antibodies and memory cells

20
Q

Describe memory cells

A
  • Responsible for the secondary immune response
    • specialised Th/B cells produced from primary immune response
    • remain in low levels in the blood
    • can divide very rapidly by mitosis if organisms encounters the same pathogen again
  • Live longer than plasma cells-decades
  • Don’t produce antibodies directly but circulate in the blood and tissue fluid
  • When they encounter the same antigen at a later date, the divide rapidly and develop into plasma cells and more memory cells
  • The plasma cells produce the antibodies needed to destroy the pathogen, while the new memory cells circulate in readiness for any future infection
    -This means memory cells provide long-term immunity against the original infection
  • An increase of antibodies is secreted at a faster rate than in primary immune response and ensures that a new infection is destroyed before it can cause harm
21
Q

What are the steps Involved in the Humoral Response?

A
  1. Complementary T helper lymphocytes bind to foreign antigen on antigen-presenting T cells. Activation of B cells by T helper cells
  2. Division of B cells into plasma cells by clonal selection
  3. Plasma cells secrete antibodies with complementary variable region to antigen
  4. Binding of antibodies to the antigens of pathogens
  5. Agglutination and phagocytosis of pathogens
22
Q

What is the role of antigen-presenting cells?

A

• Macrophage displays antigen from pathogen on its surface ( after hydrolysis in phagocytosis)
• Enhances recognition by T helper cells, which cannot directly interface with pathogens/antigens in body fluid

23
Q

Give 2 differences between specific and nonspecific immune response.

A

• nonspecific = same for all pathogens
• specific = complementary pathogen
• nonspecific = immediate
• specific = time lag

24
Q

Name the 2 types of specific immune response

A

• cell mediated
• humoral

25
Q

What is the process of the cell mediated response?

A
  1. complementary T helper lymphocytes bind to foreign antigen on APC
  2. release cytokines that stimulate
    a) clonal expansion of complementary T helper cells: become memory cells or trigger humoral response
    b) clonal expansion of cytotoxic T cells: secrete enzyme perforin to destroy infected cells
26
Q

Describe the secondary immune response

A

• faster rate of antibody production
• shorter time lag between exposure and antibody production
• higher concentration of antibodies
• antibody level remains higher after the secondary response
• pathogen usually destroyed before any symptoms

27
Q

What causes antigen variability?

A
  1. random genetic mutation changes DNA base sequence
  2. Results in different sequence of codons on mRNA
  3. Different primary structure of antigen = H-bonds, ionic bonds and disulfide bridges form in different places in tertiary structure
  4. Different shape of antigen
28
Q

How does antigen variability affect the incidence of disease?

A

• memory cells no longer complementary to antigen = individual not immune = can catch the disease more than once
• many varieties of a pathogen = difficult to develop vaccine containing all antigen types