Communicable Diseases, Disease Prevention and the Immune system Flashcards

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1
Q

what is a pathogen?

A

any micro-organism which cause disease

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2
Q

what are primary defences?

A

primary defences are mechanisms which prevent the entry of pathogenic organisms and are always non specific

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3
Q

what are secondary defences?

A

secondary defences evolved to tackle the pathogens that have entered the body and can be specific or non specific

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4
Q

what are non specific responses?

A

non- specific responses are often general and more immediate.
they involve physical barriers (such as the skin preventing pathogen entry) and some cellular processes such as phagocytosis.
(skin, blood clotting, mucous membranes, expulsive reflexes, tears, inflammation, phagocytosis)

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5
Q

what are specific responses?

A

specific responses are less rapid ad longer lasting.
these responses involve a white blood cell called a lymphocyte and take 2 forms:
- T lymphocytes (T cell) are involved in the cell mediated response
-B lymphocytes (B cell) are involved in the humoral response

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6
Q

what is keratinisation?

A

the process in which the cytoplasm of the keratinocytes is replaced by the protein keratin

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7
Q

how does the skin act as the main non- specific primary defence?

A
  • it’s made mostly of cells called keratinocytes
  • these cells are produced by mitosis at the base of the epidermis and then migrate to the surface of the skin, drying out as they move upwards
  • over 30 days keratinocytes migrate ou to the top of the skin
  • keratinisation takes place (the process in which the cytoplasm of the keratinocytes is replaced by the protein keratin)
  • these cells eventually die by the time they reach the surface of the skin where they act as barrier to the pathogen
  • eventually the dead cells slough off and are replaced
  • Also lots of harmless microbes called skin flora also live on the skin preventing pathogenic microbes from colonising on the sin by competing with them for nutrients
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8
Q

how does blood clotting and wound repair act as a non specific primary defence?

A
  • when a blood clot dries, it forms a temp seal called a scab allowing the skin to repair
  • the scab shrinks as it dries bringing the edges of the cut together
  • to trigger blood clotting, platelets and damages tissues release clotting factors which activate an enzyme cascade
  • to repair the skin, fibrous collagen is deposited under the scab, and the stem cells divide by mitosis in the epidermis to produce new cells
  • the new cells then migrate to the edges of the cut before differentiating to form new cells
  • these new cells then migrate to the edges of the cut before differentiating to form new skin cells
  • they’re supplied with oxygen and nutrients by the growth of new blood vessels
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9
Q

how does the mucus membrane act as a non specific primary defence?

A
  • exchange surfaces where oxygen and nutrients enter the blood are thinner and more exposed to pathogens
  • these areas are protected by mucus membrane, specialised epithelial tissue covered by mucus
  • in the airways, goblet cells and glands secrete mucus, which traps pathogens
  • the epithelium lining the airways contains ciliated cells from which tiny hair-like structures called cilia protrude
  • the cilia waft in a coordinated fashion to move the mucus (containing trapped pathogens) to the top of the trachea
  • the mucus is then swallowed and moves down the oesophagus before entering the stomach
  • the low pH of stomach acid kills the pathogens as their enzymes become denatured
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10
Q

how do expulsive reflexes act as a non specific primary defence?

A
  • some pathogens can release toxins
  • areas which are at risk of infection are very sensitive to pathogens and their toxins
  • when these areas are irritated, they respond with a expulsive reflex (coughing, sneezing, vomiting)
  • this reflex causes are or fluid to be suddenly forced out of the body which carries the pathogen put with it
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11
Q

what are some non specific chemical defences and how do the work?

A
  • saliva, tears nasal secretion
  • these contain and enzyme called a lysozyme
  • lysozyme kills bacteria by breaking down the bacterial cell wall
  • the lysis of the pathogen prevents it from entering nose, eyes and mouth so it cannot cause disease
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12
Q

what is inflammation?

A

when a pathogen infects a tissue- it can cause a tissue to turn red and swell.
-this helps destroy invading pathogens

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13
Q

how does inflammation act as a non specific primary defence?

A

1-the pathogen is detected in the tissues by mast cells (a specialised type of phagocytic cell
2-pathogen detection triggers mast cells to release the cell- signalling chemical histamine. Histamine causes vasodilation, thus making the capillary walls in tissues more permeable to white blood cells
3-more white blood cells can therefore move out of the capillaries into the tissue fluid and reach the site of the infection
4-vasodilation causes more tissue fluid to be produces, which leads to swelling (oedema)
5-the excess tissue fluid is then drained into the lymphatic system where other immune cells are stored. these immune cells can then attack the pathogens present in the tissue fluid

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14
Q

what is phagocytosis?

A

this is where a specific type of white blood cell (called a phagocyte) engulfs and digests pathogens to stop them causing damage.
-some phagocytes can travel in the blood and move out into the tissues when they are needed

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15
Q

what is phagocytosis used for?

A

-phagocytosis is also used to remove dead, damaged or abnormal

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16
Q

what are some example of phagocytes?

A

-macrophages and neutrophils

17
Q

where are monocytes(macrophage precursor cells) and neutrophils made?

A

both are made in the bone marrow

18
Q

what is the difference between neutrophils and macrophages?

A

neutrophils die quickly after a few days whereas macrophages are long lived cells

19
Q

what structure enables neutrophils to perform its function?

A

neutrophils possess multilobed nuclei.

  • when any pathogen infects a tissue, neutrophils arrive first, move out of the blood into the tissue and engulf pathogenic cells
  • neutrophils usually die after ingesting pathogens and then collect to from pus
20
Q

explain the process of phagocytosis

A

1-the pathogen has chemical markers on its cell surface membrane called antigens. Attached to these antigens are non- specific protein molecules called opsonins which enhance the ability of phagocytic cells to carry out their function. The receptors on the surface of the phagocyte can recognise and attach to these opsonins
2-the pathogen is then engulfed by the phagocyte to form a vesicle called a phagosome
3-the lysosomes within the phagocyte move towards and fuse with the phagosome, releasing lysozymes into the phagosome. The lysozymes are enzymes which destroy ingested bacteria by hydrolysing the cell walls in a process similar to digestion
4-the products of the pathogen breakdown are absorbed into the phagocyte

21
Q

what is the difference between monocytes and macrophages?

A

monocytes are present in the blood and upon entry to the tissues and lymph nodes they become macrophages

22
Q

how do macrophages help protect against future infections?

A
  • macrophages do not fully digest the pathogen
  • it saves the antigen from the pathogen cell surface and moves this antigen to a special protein complex
  • the macrophage then exhibits this protein complex its cell surface and becomes an antigen presenting cell (APC)
  • other cells of the immune system can recognise antigens presented by APCs without confusing the macrophage for a foreign pathogen
23
Q

how are phagocytes specialised to perform their function?

A
  • phagocytes have well developed cytoskeletons, allowing them to change shape to engulf pathogens and move lysosomes around
  • they have many mitochondria to release energy required for cell movement
  • they contain ribosomes to synthesise the lysosome enzymes
  • neutrophils have a lobed nucleus to help them squeeze through narrow gaps between cells in the tissues