Chapter 11.1 Flashcards

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1
Q

what are Phagocytes

A

are white blood cells that are produced continuously in the bone marrow

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2
Q

where are phagocytes stored

A

in the bone marrow before being distributed around the body in the blood

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3
Q

function of phagocytes

A
  • They are responsible for removing dead cells and invasive microorganisms
  • They carry out what is known as a non-specific immune response
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4
Q

There are two main types of phagocyte

A
  • Neutrophils
  • Macrophages
  • As both are phagocytes, both carry out phagocytosis (the process of recognising and engulfing a pathogen) but the process is slightly different for each type of phagocyte
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5
Q

Neutrophils

A
  • Neutrophils travel throughout the body and often leave the blood by squeezing through capillary walls to ‘patrol’ the body tissues
  • During an infection, they are released in large numbers from their stores
  • However, they are short-lived cells
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6
Q

The stages of phagocytosis, as carried out by a neutrophil

A
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7
Q

Neutrophils mode of action

A
  • Chemicals released by pathogens, as well as chemicals released by the body cells under attack (eg. histamine), attract neutrophils to the site where the pathogens are located (this response to chemical stimuli is known as chemotaxis)
  • Neutrophils move towards pathogens (which may be covered in antibodies)
  • The antibodies are another trigger to stimulate neutrophils to attack the pathogens (neutrophils have receptor proteins on their surfaces that recognise antibody molecules and attach to them)
  • Once attached to a pathogen, the cell surface membrane of a neutrophil extends out and around the pathogen, engulfing it and trapping the pathogen within a phagocytic vacuole
  • This part of the process is known as endocytosis
  • The neutrophil then secretes digestive enzymes into the vacuole (the enzymes are released from lysosomes which fuse with the phagocytic vacuole)
  • These digestive enzymes destroy the pathogen
  • After killing and digesting the pathogens, the neutrophils die
  • Pus is a sign of dead neutrophils
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8
Q

Macrophages

A
  • Macrophages are larger than neutrophils and are long-lived cells
  • Rather than remaining in the blood, they move into organs including the lungs, liver, spleen, kidney and lymph nodes
  • After being produced in the bone marrow, macrophages travel in the blood as monocytes, which then develop into macrophages once they leave the blood to settle in the various organs listed above
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9
Q

Mode of action: Macrophages

A
  • Macrophages play a very important role in initiating an immune response
  • Although they still carry out phagocytosis in a similar way to neutrophils, they do not destroy pathogens completely
  • They cut the pathogens up so that they can display the antigens of the pathogens on their surface (through a structure called the major histocompatibility complex)
  • These displayed antigens (the cell is now called an antigen-presenting cell) can then be recognised by lymphocytes (another type of white blood cell)
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10
Q

Lymphocytes

A

are another type of white blood cell

  • They play an important part in the specific immune response
  • They are smaller than phagocytes
  • They have a large nucleus that fills most of the cell
  • They are produced in the bone marrow before birth
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11
Q

There are two types of lymphocytes (with different modes of action). The two types of lymphocytes are:

A

-B-lymphocytes (B cells)

T–lymphocytes (T cells)

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12
Q

B-lymphocytes (B cells)

A

remain in the bone marrow until they are mature and then spread through the body, concentrating in lymph nodes and the spleen

  • Millions of types of B-lymphocyte cells are produced within us because as they mature the genes coding for antibodies are changed to code for different antibodies
  • Once mature, each type of B-lymphocyte cell can make one type of antibody molecule
  • At this stage, the antibody molecules do not leave the B-lymphocyte cell but remain in the cell surface membrane
  • Part of each antibody molecule forms a glycoprotein receptor that can combine specifically with one type of antigen
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13
Q

If that antigen enters the body

A

-B-lymphocyte cells with the correct cell surface receptors will be able to recognise it and then divide by mitosis (clonal selection)

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14
Q

-During a primary immune response, B-lymphocytes

A

divide repeatedly by mitosis (clonal expansion) and differentiate into two main types of cell:

  • Plasma cells
  • Memory cells
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15
Q

The maturation of B-lymphocytes

A
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16
Q

T-lymphocytes

A
  • Immature T-lymphocytes leave the bone marrow to mature in the thymus
  • Mature T-lymphocytes have specific cell surface receptors called T cell receptors
  • These receptors have a similar structure to antibodies and are each specific to one antigen
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17
Q

T-lymphocytes are activated when they

A

encounter (and bind to) their specific antigen that is being presented by one of the host’s cells (host cells being the human’s own cells)

-This antigen-presenting host cell might be a macrophage or a body cell that has been invaded by a pathogen and is displaying the antigen on its cell surface membrane

18
Q

These activated T-lymphocytes (those that have receptors specific to the antigen) divide

A

by mitosis to increase in number (similar to the clonal selection and clonal expansion of B-lymphocytes) and differentiate into two main types of T cell:

  • Helper T cells
  • Killer T cells
19
Q

Neutrophils in the blood increase in number during

A

bacterial infections and when tissues become inflamed and die

20
Q

Lymphocytes in the blood increase in number during

A

viral infections and tuberculosis

21
Q

Blood tests are regularly carried out by doctors to help them diagnose

A

diseases and assess the success of treatments

-The numbers of different types of white blood cells in the blood can provide information about what type of infection someone might have, the severity of the infection, or whether the treatment that has been prescribed is working

22
Q

The two groups of stem cells in the bone marrow are:

A
  • Myeloid stem cells – differentiate to form red blood cells, neutrophils, monocytes and platelets
  • Lymphoid stem cells – differentiate to form lymphocytes (both B-lymphocytes and T-lymphocytes)
  • These stem cells divide in a rapid but controlled way, producing very large numbers of differentiated white blood cells that carry out specific functions within an immune response
23
Q

Leukaemia

A
  • Leukaemias are cancers of these bone marrow stem cells
  • When someone has leukaemia, these stem cells divide rapidly but uncontrollably, producing large numbers of cells that do not differentiate properly (known as malignant cells) and therefore do not function appropriately
  • The malignant cells also fill the bone marrow and disrupt the production of normal blood cells (including red blood cells and platelets). They then enter the blood and the lymphatic system
24
Q

There are two types of leukaemia, each having a slightly different effect:

A
  • Myeloid leukaemias
  • Lymphoblastic leukaemias
25
Q

Myeloid leukaemias

A

neutrophil-producing stem cells divide rapidly and uncontrollably (number of immature neutrophil cells increases)

26
Q

Lymphoblastic leukaemias are

A

– lymphocyte-producing stem cells divide rapidly and uncontrollably (number of immature lymphocyte cells increases)

27
Q

Myeloid and lymphoblastic leukaemias can take two forms:

A
  • Acute form – acute leukaemias develop rapidly, have severe effects and must be treated as soon as a diagnosis is made
  • Chronic form – chronic leukaemias develop slowly (some take many years) and changes in blood cell counts are monitored over time so that treatment can be given when it has the highest chance of curing the disease
28
Q

immature white blood cells disrupt the balance of components in the blood: in what way

A
  • The number of red blood cells or platelets decreases, resulting in anaemia and an increased risk of excessive bleeding
  • The number of mature neutrophils and lymphocytes decreases, resulting in immunosuppression (increased susceptibility to infections)
29
Q

antigens

A
  • Every cell in the human body has markers that identify it
  • Microorganisms (both pathogenic and non-pathogenic), such as bacteria and viruses, also have their own unique markers
  • they allow cell-to-cell recognition
  • Antigens are found on cell surface membranes, bacterial cell walls, or the surfaces of viruses
  • Some glycolipids and glycoproteins on the outer surface of cell surface membranes act as antigens
30
Q

Antigens produced by the organism’s own body cells (those that the immune system does not recognise as foreign antigens)

A

are known as self antigens

-Self antigens do not stimulate an immune response

31
Q

Antigens not produced by the organism’s own body cells (those that the immune system recognises as being foreign eg. the antigens found on pathogenic bacteria and viruses or if a person receives a different blood type during a transfusion) are known as

A
  • non-self antigens
  • Non-self antigens stimulate an immune response
32
Q

During an immune response, B-lymphocytes form two types of cell:

A

plasma cells and memory cells

33
Q

Memory cells form the basis of

A

immunological memory – the cells can last for many years and often a lifetime

34
Q

There are two types of immune response:

A
  • Primary immune response (responding to a newly encountered antigen)
  • Secondary immune response (responding to a previously encountered antigen)
35
Q

Primary immune response

A
  • When an antigen enters the body for the first time, the small numbers of B-lymphocytes with receptors complementary to that antigen are stimulated to divide by mitosis
  • As these clones divide repeatedly by mitosis (the clonal expansion stage) the result is large numbers of identical B-lymphocytes being produced over a few weeks
  • Some of these B-lymphocytes become plasma cells that secrete lots of antibody molecules (specific to the antigen) into the blood, lymph or linings of the lungs and the gut
  • These plasma cells are short-lived (their numbers drop off after several weeks) but the antibodies they have secreted stay in the blood for a longer time
  • The other B-lymphocytes become memory cells that remain circulating in the blood for a long time
  • This response to a newly encountered pathogen is relatively slow
36
Q

clonal selection

A

When an antigen enters the body for the first time, the small numbers of B-lymphocytes with receptors complementary to that antigen are stimulated to divide by mitosis

37
Q

Secondary immune response

A
  • If the same antigen is found in the body a second time, the memory cells recognise the antigen, divide very quickly and differentiate into plasma cells (to produce antibodies) and more memory cells
  • This response is very quick, meaning that the infection can be destroyed and removed before the pathogen population increases too much and symptoms of the disease develop
  • This response to a previously encountered pathogen is, relative to the primary immune response, extremely fast
38
Q

T-lymphocytes also play a part in the secondary immune response

A

They differentiate into memory cells, producing two main types:

  • Memory helper T cells
  • Memory killer T cells
  • Just like the memory cells formed from B-lymphocytes, these memory T cells remain in the body for a long time
  • If the same antigen is found in the body a second time, these memory T cells become active very quickly
39
Q

The effect of Myasthenia gravis at a neuromuscular junction

A
40
Q

autoimmune diseases:

A
  • Autoimmune disease occur because the body’s immune system attacks one or more self antigens (antigens that are produced by human body cells)
  • During the maturation of T cells, many of the T cells are destroyed because they have incorrect T cell receptors that are complementary to self-antigens (these T cell surface receptors should only be complementary to non-self antigens)
  • However, some of these incorrect T cells evade destruction and become activated to stimulate an immune response against these self-antigens (ie. against the body itself)
  • This starts an attack (usually involving antibodies and killer T cells) against the body
  • In some autoimmune diseases, this attack is localised and directed against one organ (eg. Type 1 diabetes). In others, it is directed against the whole body (eg. lupus)
41
Q

Myasthenia gravis (MG)

A
  • That targets the neuromuscular junctions between motor neurones (nerve cells) and skeletal muscle cells
  • That causes the immune system to block receptor proteins at the neuromuscular junction (antibodies are produced, which then bind to these receptor proteins, blocking the transmission of impulses from motor neurons)
  • Where muscles fibres absorb the receptor-antibody complexes and destroy them
  • That results in non-functioning receptors which results in muscle cells receiving no stimulation and can lead to muscle tissue starting to break down
42
Q

Myasthenia gravis (MG) meaning

A

grave (serious) muscle weakness, is an autoimmune disease: