Cells (Immunity) - Adaptive Immune Response Flashcards

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1
Q

What is the difference between T and B cells?

A

T-cells respond to antigens presented on the surface of our own cells (antigen presenting cells). They have receptor proteins that can detect antigens and form antigen-receptor complexes.

B-cells respond to free antigens found in our blood plasma and tissue fluid. They display and secrete antibodies that can detect antigens and form antigen-antibody complexes.

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2
Q

What is the humoral response?

A

Produces antibodies that are complementary to the antigen. They destroy the pathogen and their toxins. Called ‘humoral’ because it is triggered by antigens in the body’s ‘humour’ (body fluids).

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3
Q

What are the phases of the immune response?

A

physical barrier -> phagocytosis -> cell-mediated immunity -> humoral immunity

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4
Q

What is immunity?

A

Immunity is the ability of organisms to resist infection by protecting against disease-causing microorganisms or their toxins that invade their bodies due to the presence of antibodies. It involved the recognition of foreign material (antigens).

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5
Q

What is an antigen?

A

An antigen is any part of an organisms or substance that is recognised as non-self (foreign) by the immune system and stimulates an immune response. Antigens are usually proteins 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. The antibodies are specific to the antigen and react with it to make it harmless.

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6
Q

What is the difference between the specific and non-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.

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7
Q

What does the specific immune response depend on?

A

The specific immune response depends on a type of white blood cell called a lymphocyte. Lymphocytes are produced by stem cells in the bone marrow. There are two types of lymphocytes, each with its own role in the immune response.

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8
Q

What are B-lymphocytes (B cells)?

A

B lymphocytes (B cells) are so called because they originate and 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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9
Q

What are T-lymphocytes (T cells)?

A

T lymphocytes (T cells) are so called because they originate in bone marrow and mature in the thymus gland. They are associated with cell-mediated immunity, that is immunity involving body cells.

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10
Q

What do lymphocytes respond to?

A

Lymphocytes respond to an organism’s own cells that have been infected by non-self material from a different species, e.g. a virus. They also respond to cells from other individuals of the same species because these are genetically different. These therefore have different antigens on their cell-surface membrane from the antigens on the organism’s own cells.

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11
Q

How do 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 membrane.
  • 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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12
Q

What are antigen presenting cells?

A

Cells that display foreign antigens on their surface are called antigen-presenting cells because they can present antigens of other cells on their own cell-surface membrane.

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13
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 acts as an APC and places antigens from the pathogen on its cell-surface membrane.
  3. Helper T cells are activated by antigen presenting cells. 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:
    - develop into memory cells that circulates in the blood and tissue fluid in readiness to respond to future infections by the same pathogen (provide long-term immunity)
    - stimulate phagocytes to engulf pathogens by phagocytosis
    - stimulate B cells to divide and secrete their antibody specific to the pathogen
    - activate cytotoxic T cells to kill infected cells by perforin making holes in their cell-surface membranes

Helper T cells also produce cytokines that increase proliferation of these cells, and produce interferons which increase the immune response.

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14
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 causing apoptosis.
  • They produce a protein called perforin that binds to the cell-surface membrane of the target cell and perforates the membrane.
  • These holes mean the cell membrane becomes freely permeable to all substances and the cell dies as a result.
  • Before apoptosis, interferons are released. Interferons inhibit viral replication in the surrounding area, and increase the anti-viral defence mechanisms of other body cells.
  • Many viruses are released during target cell apoptosis. Upon recognising a particular virus, the antibodies bind to it, and opsinate it. Opsination of a virus covers its attachment proteins which prevent it from binding to and infecting other cells.
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15
Q

How do B cells divide?

A

The first phase of the specific response to infection is the mitotic division of specific T cells to form a clone of the relevant T cells to build up their numbers. Some of these T cells stimulate B cells to divide. It is the B cells that are involved in the next phase of the immune response: humoral immunity.

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16
Q

Why is it called humoral immunity?

A

Humoral immunity is so called because it involves antibodies, and antibodies are soluble in the blood and tissue fluid of the body. An old-fashioned word for body fluids is ‘humour’.

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17
Q

How many types of B cells are there?

A

There are many different types of B cell, possibly as many as ten million, and each B cells starts to produce a specific antibody that responds to one specific antigen. When an antigen, for example, a protein on the surface of a pathogen, foreign cell, 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. The antibody therefore attaches to this complementary antigen.

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18
Q

How does the antigen enter the B cell?

A

The antigen enters the B cell by endocytosis and gets presented on its surface (processed).

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19
Q

What is clonal selection?

A

T cells bind to the processed antigens and stimulates 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.

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20
Q

What are monoclonal antibodies?

A

In practice, 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 cell.

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21
Q

Are B cells produced in response to a pathogen?

A

B cells with the appropriate antibody to bind to antigens of a pathogen are not produced in response to the pathogen. They are present from birth. Being present, they simply multiply in response to the pathogen.

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22
Q

What are plasma cells?

A

Plasma cells 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. The plasma cells are therefore responsible for the immediate defence of the body against infection. The production of antibodies is known as the primary immune response.

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23
Q

What are memory cells?

A

Memory cells are responsible for the secondary immune response. Memory cells live considerably longer than plasma cells, often for decades. These cells do not produce antibodies directly, but circulate in the blood and tissue fluid. When they encounter the same antigen at a later date, they 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. In this way, memory cells provide long-term immunity against the original infection. An increased quantity of antibodies is secreted at a faster rate than in the primary immune response. It ensures that a new infection is destroyed before it can cause any harm - and individuals are often totally unaware that they have ever been infected.

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24
Q

Explain the role of B cells in immunity.

A

B cells are specific against a particular antigen and pathogen. Similarly, a particular B cell will be activated by a particular helper T Cell.

  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 proliferate via mitosis. They differentiate 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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25
Q

What is the structure of antibodies?

A

Composed of four polypeptide chains:

  • 2 heavy chains
  • 2 light chains
  • joined by disulphide bonds

Form a Y-shaped structure:

  • the stem = constant region
  • the ends of the arms = variable regions that bind to the antigen
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26
Q

What does the variable region do?

A

The variable region binds to the antigen forming an antibody-antigen complex. Cloned B cells will only make antibodies with the same shape variable region - they are genetically identical.

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27
Q

What is the specific immune response?

A

The specific immune response is antigen specific and produces responses specific to one type of pathogen only.

28
Q

What are B effector or plasma cells?

A

antibody producing cells

29
Q

What are T helper cells?

A

stimulates B cells and T killer cells to divide

30
Q

What are T killer cells?

A

destroy pathogen infected cells

31
Q

What are antibodies? What is agglutination?

A

In the humoral response, plasma cells produce antibodies. These are made of four polypeptide chains forming a Y shaped structure. These are complementary to only a single antigen. They work by forming an antigen-antibody complex which serve as markers for phagocytes to destroy attached cells. Due to antibodies having two binding sites they can also clump cells together making them easier for phagocytes to find. This process is called agglutination.

32
Q

What are B lymphocytes responsible for?

A

Producing antibodies which are protein molecules that are specific to an antigen and neutralise it.

33
Q

Where are antibodies found?

A

Antibodies are present in the plasma and can bind to specific antigens free in bodily fluids or antigens on cells.

34
Q

What is direct contact?

A

Direct contact happens when the lymphocyte comes across the pathogenic cells in the lymph nodes.

35
Q

What is indirect contact?

A

Indirect contact happens when the lymphocyte comes across an antigen presenting cell which phagocytosed the pathogen.

36
Q

What are interleukins?

A

Other immune cells like macrophages secrete a type of cell signalling molecule called interleukins. These interleukins bind specifically to the selected lymphocyte and cause it to divide by mitosis to produce lots of clones.

37
Q

What is clonal expansion?

A

When the number of cells is increased by mitotic division.

38
Q

What can memory T cells differentiate into?

A

Memory T cells are activated and can differentiate into T killer cells and T helper cells.

39
Q

What is the primary response?

A
  • Antigen has entered the body
  • Activates a slow response – not many B cells to bind (millions present but all have different
    receptors)
  • Eventually the body will make enough antibody to overcome the infection (plasma B cells, short lasting)
  • Usually during this time the infected person shows symptoms
  • After being exposed to an antigen, both T- and B- cells produce memory cells (stay in the body)
  • These memory cells produce specific antibodies needed to bind to the antigen (responds quickly to the second infection)
40
Q

What is the secondary response?

A
  • If the same pathogen enters again
  • Quicker, stronger immune response
  • Clonal selection – memory B-cells activated and divide into plasma cells, produce right antibody to the antigen
  • Memory T cells – activate and divide to produce the Tc cells that kill the cell carrying the antigen
  • Secondary response often gets rid of the pathogen before you begin to show any symptoms
41
Q

Why is the secondary response quicker?

A

Because clonal selection and clonal expansion are skipped. Plasma cells produce antibodies much sooner and more rapidly. This is usually quick enough to prevent any symptoms from appearing.

42
Q

What is the thymus gland?

A

The thymus gland is located above the heart on the wind pipe. It is large in infants but regresses with age. Immature T cells move to the thymus to mature before migrating to other lymphatic organs.

43
Q

What 2 kinds of cells to B cells differentiate into?

A
  • Memory cells: Some B cells differentiate into long-lived memory cells. When these cells encounter the same antigen again (even years or decades later), they rapidly differentiate into antibody-producing plasma cells. They are involved in the secondary immune response, when the body is reinfected by the same pathogen. Upon secondary infection by the same pathogen, memory B cells rapidly differentiate into plasma B cells to quickly produce antibodies against the pathogen.
  • Plasma cells: When stimulated by an antigen, some B cells differentiate into plasma cells, which are short lived and secrete large amounts of antibodies against a particular antigen into the blood system. The antibodies then inactivate the circulating antigens. Their main function is during the primary immune response.
44
Q

What 4 kinds of cells to T cells differentiate into?

A
  • Helper T cell: Activates cytotoxic T cells and other helper T cells. They are necessary for B cell activation.
  • T cell for delayed hypersensitivity: Protects against pathogens. Causes transplant rejection and inflammation in allergic reactions.
  • Suppressor T cell: Regulates immune response by turning it off when no more antigen is present.
  • Cytotoxic T cell: Destroys target cells on contact. Recognises tumour (cancer) or virus infected cells by their surface (antigens and MHC markers).
45
Q

How do antibodies inactivate antigens?

A
  • neutralisation: antibodies bind to viral binding sites and coat bacterial toxins.
  • sticking together particulate antigens: solid antigens such as bacteria are stuck together in clumps.
  • precipitation of soluble antigens: soluble antigens are stuck together to form precipitates.
  • activation of complement: tags foreign cells for destruction by phagocytes and complement.
46
Q

What is the immune system?

A

This consists of a number of lymphoid organs linked by lymphatic vessels and capillaries. The lymphoid organs house billions of lymphocytes which are responsible for identifying and eliminating infectious parasites.

47
Q

What are lymphocytes?

A

Large lymphocytes are formed from stem cells in the bone marrow. The B-lymphocytes make antibodies (humoral response) and are found in the lymphoid organs (except thymus). The T-lymphocytes develop in the thymus, and are concerned not only with cellular immunity but also with the regulation of the humoral response by the B-lymphocytes.

48
Q

What are phagocytes?

A

Cells, e.g. neutrophils and eosinophils, which carry out phagocytosis (the ingestion and destruction of microbes and other particulate matter). The cells can wander around the body by amoeboid action and will congregate in huge numbers at a site of infection in order to engulf any microbial material. Phagocytes are attracted to sites of infection by chemotaxis.

49
Q

What is the clonal selection theory?

A

At birth the lymphoid system is thought to contain as many as one hundred million different clones of small lymphocytes, each one committed by the shape of its antigen receptors to recognise just one antigen grouping. Each clone consists of less than a hundred cells but there are more than enough clones to recognise all the different antigen groupings that might be encountered throughout life. (A clone is a population of genetically identical cells formed by mitosis). Thus if the lymphocytes encounter a particular antigen only a few cells (one clone) will recognise it and respond.

50
Q

What are T-cells and cellular immunity?

A

The invading pathogen are initially phagocytosed by macrophages. Some of the macrophages only partially digest the pathogen and then display the antigen on their cell surfaces, together with one of the body’s own antigenic recognition factors. These two antigens are then presented to and activate the T-lymphocytes. Such activated cells are said to be sensitised, and will increase in size and divide many times to form a clone of genetically identical cells. These cells then differentiate to form clones of killer, memory, amplifier, helper, suppressor and delayed hypersensitivity T-cells, which all have particular roles to play in immunity.

51
Q

What are the major roles of killer/cytotoxic T-cells?

A
  1. Leave lymphoid tissue and attach to and destroy invading cells.
  2. Secret lymphokines which:
    - stimulate T-cell growth, division and differentiation
    - cause non-sensitised lymphocytes nearby to become killer T-cells
    - attract macrophages to the area and also stimulate them to increase activity
  3. Secrete interferons which inhibit viral replication.
52
Q

What are the major roles of memory cells?

A

Are programmed to remember the original invading antigen. They remain stored in the lymphoid tissue and if the same antigen is encountered again it is destroyed before disease symptoms occur.

53
Q

What are the major roles of helper T-cells?

A
  1. Co-operate with B-cells to induce and amplify antibody production.
  2. Stimulate multiplication of killer T-cells, thus enhancing the immune response.
54
Q

Which cells remain in the lymphoid tissues?

A

Only the memory cells remain in the lymphoid tissues, the other cells migrate out into other tissues and organs. During the processing and presentation of antigens, macrophages secrete lymphokines which stimulate T-cell growth, division and differentiation.

55
Q

What are B-cells and humoral immunity?

A

Unlike T-cells, B-cells do not attack pathogens directly. Instead, they remain in the lymphoid tissue (spleen, lymph nodes) and produce antibodies.

56
Q

What are the major roles of plasma B-cells?

A

Secrete antibodies into the circulation. The antibodies are specific to the pathogenic antigen, which is destroyed. The rate of antigen secretion can be as high as 2000 molecules per second per cell and the active plasma cell will live for 4-5 days.

57
Q

What are the major roles of memory B-cells?

A

These are programmed to remember the specific antigen and to respond very rapidly should the body be challenged by that antigen on a subsequent occasion, thus preventing further infection.

58
Q

What is the nature of antigens?

A

An antigen has two important characteristics:

  1. immunogenicity - ability to stimulate the formation of specific antibodies.
  2. reactivity - ability of the antigen to react specifically with the antibodies.
59
Q

What is the nature of antibodies?

A

Most antibodies contain two pairs of polypeptide chains. Two of the chains are identical to each other and are referred to as heavy chains. The other two chains are also identical to each other and are referred to as light chains. The antibody consists of two identical halves held together by disulphide bonds. Each half consists of a heavy chain and a light chain, also joined together by a disulphide bond. Under the electron microscope, they appear T shaped before combination with antigen and become Y shapes on combination with the antigen.

There are two distinct regions within the light and heavy chains. The tops of the chains are called the variable portions and are the sites which bind to the antigen. The variable portion is different for each kind of antibody and allows the antibody to recognise and attach specifically to a particular antigen. The remainder of each polypeptide chain is called the constant portion.

60
Q

Why is AIDS a problem of immunity?

A

Acquired Immune Defiency Syndrome is caused by the Human Immunodeficiency Virus. The HIV virus binds to special receptors, called CD4 receptors, which are on the surfaces of T-helper cells. These are killed by the virus and thus the immune response is impaired. This immunodeficiency exposes the infected person to infection by other pathogenic organisms which will eventually result in death.

61
Q

Why is autoimmune disease a problem of immunity?

A

Autoimmune disease is where the body produces antibodies against some of its own tissues and thus these tissues are destroyed, resulting in disease.

62
Q

Why is tissue rejection a problem of immunity?

A

Tissue rejection is a problem in treating patients by transplantation. The implanted organs are recognised as foreign and thus antibodies are produced which may damage or destroy them. This is known as tissue rejection. The problems may be reduced by transplanting closely matching tissues (with same or similar surface/HLA antigens) and by using drugs which suppress the immune response, such as cyclosporine.

63
Q

Why is incompatible blood transfusion a problem of immunity?

A

Incompatible blood transfusion with either ABO groups or Rhesus groups will cause a problem if the immune system has previously been challenged by the wrong blood and thus has an immunological memory. The antibodies produced will clump the red cells together and these clumps can block capillaries and small arterioles in the kidneys, heart, brain or anywhere in the body. This could result in death.

64
Q

How is the adaptive response activated?

A
  • Antigen presenting cells activate the adaptive response.
  • The three major leukocytes that carry out antigen presentation are dendritic cells, neutrophils and macrophages.
  • APCs, macrophages and dendritic cells phagocytise foreign pathogens.
  • They represent their antigens to the innate immune system.
65
Q

How are T-cells formed?

A
  • T-cells originate in the bone marrow, where they are formed from adult (hematopoietic) stem cells.
  • Immature T-cells (thymocytes) are transported to the thymus gland.
  • Thymocytes undergo maturation and clonal deletion in the thymus.
66
Q

What is immunological memory?

A
  • When memory B Cells allow the body to fight a disease more quickly and effectively than the primary infection.
  • This provides many organisms with long term immunity against particular pathogens.