C3.2 Defence against disease Flashcards

1
Q

What are pathogens

A

Pathogens are disease-causing organisms like viruses, bacteria, fungi and protists that result in disease upon entry into the body

[most not pathogenic to humans but have exceptions]

  • pathogens use human tissues as food and shelter but their means of growth and secretions can cause us harm
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2
Q

NOS 1

A

meticulous observations can lead to break throughs
- 1854, major cholera outbreak in suburb of London, UK
- Vibio cholerae bacteria that causes cholera is found in faeces of infected Indivs
- common practice in 1800s to empty waste into areas in front of homes –> bacteria moved through soil and infected drinking well used by many
- a physician named JOHN SNOW suspected cholera was transmitted in water supplies
- he created a map of all known infections and found one particular well was used by all
- the well was closed –> number of cholera infections fell
- info & map by SNOW formed basis of modern epidemiology studies that trace outbreaks

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3
Q

NOS 2

A

In mid 1800s, physician IGNAZ SEMMELWEIS in Vienna, Austria studied a lethal diseases called childbed fever
- disease alrdy had alarming high rates of infection & death in Vienna maternity wards
- semmelweis noted a difference in infection rates btw 2 maternity wards
- one ward staffed by midwifes, one staffed by other physicians and medical students
- rate of infection & death much faster in physcians’ ward
- he eliminated specific differences btw 2 wards, besides who staffed them
- one difference which proved to be consequential is that physicians often carried out autopsies before childbirth
- he postulated that the physicians were carrying small “particles” that caused the disease from autopsies to pregnant women
- he ordered all to wash hands w chlorine solution before treating patients –> immediate improvement in infection rate

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4
Q

Lines of defence against pathogens

A
  1. First line of defence - surface barriers that prevent entry of pathogens into body
    - skin, mucous membrane, secretions of skin & mucous membrane
  2. Second line of defence - non-specific phagocytes & internal mechanisms that comprise innate immunity
    - phagocytic leukocytes
    - antimicrobial proteins
    - inflammatory response
    - fever
  3. Third line of defence - specific lymphocytes that produce antibodies as part of adaptive immune response
    - lymphocytes
    - antibodies
    - memory cells
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5
Q

Skin and mucous membrane as primary defence [physical & chemical barrier to pathogens]

A

Skin has 2 primary layers:
1. Dermis (underneath)
- sweat glands, capillaries, sensory receptors, dermal cells which give structure and strength to skin
2. Epidermis (top layer)
- constantly replaced as the underlying dermal cells die and move upwards
- layer of dead cells forms physical barrier against most pathogens bc it is not alive
- as long as skin is intact, we are protected from most pathogens

BUT pathogens can enter body through a few locations not covered by skin - these entry points are lined with tissue cells that form a mucous membrane
- cells of mucous membranes produce and secrete a lining of sticky mucus
- mucus traps incoming pathogens –> preventing them from reaching cells they can infect
- some mucous membrane tissues lined with cilia [hair-like extensions capable of wave-like movement –> movement carries trapped pathogens up and out of mucous-lined tissues like trachea]

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6
Q

Areas with mucous membrane

A

Trachea - tube that carries air to and from lungs
Nasal passages - tubes that allow air to enter nose then trachea
Urethra - tube that carries urine from bladder to outside
Vagina - reproductive tract leading from uterus to outside

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7
Q

Sealing of cuts in skin by blood clotting

A

Plasma proteins circulate in the blood plasma:
1. Prothrombin
2. Fibrinogen
they circulate in the blood plasma and remain inactive till events like bleeding occur

Cell fragments that circulate in bloodstream: Platelets
- they form in the bone marrow, along w RBC (erythrocytes) and WBC (leucocytes) but don’t remain as entire cells
- one breaks down into many fragments and each becomes a platelet –> they don’t have nucleus and hence has short cellular life span of 8-10days

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8
Q

Process of blood clotting

A
  1. when cells of blood vessels damaged, chemicals are released to stimulate platelets to adhere to damaged area –> forming a “plug”
  2. damaged tissue and platelets release chemicals called clotting factors that convert prothrombin to thrombin
  3. thrombin is an active enzyme that catalyses the conversion of soluble fibrinogen into relatively insoluble fibrin
  4. fibrin is a fibrous protein that forms a mesh-like network which helps stabilise platelet plug
  5. more and more cellular debris gets trapped in fibrin mesh –> stable clot is formed, preventing further blood loss & entry of pathogens
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9
Q

Innate immune system (First layer of human immunity)

A
  • responds to broad categories of pathogens & don’t change during a person’s lifetime
  • recognise things that belong and those that don’t belong in human body
  • the molecules of foreign/ non self entities are called ANTIGENS which can trigger an immune response
  • the innate immune system involves the activation of a group of leucocytes (WBC) called phagocytes which are able of engulfing invading materials by endocytosis
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10
Q

Adaptive immune response (Second layer of human immunity)

A
  • develops over time & only after exposure to specific antigens of specific pathogens
  • first exposure to specific antigen leads to series of cellular events culminating in molecules and cells that are longed lived and have ability to defend body against specific pathogen
  • specific long-lived WBC formed during first exposure are memory cells
  • upon second exposure to same pathogen, these specific memory cells are activated quickly –> very effective in fighting a pathogen
  • adaptive immune response become more effective with age, as a person becomes exposed to more pathogens
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11
Q

Phagoctyes

A

They are leucocytes (WBC) capable of AMEOBOID MOVEMENT –> can purposefully extend sections of their plasma membrane, followed by cytoplasm and organelles
- phagocytes use this motion to squeeze their way through capillaries so that they can leave & enter bloodstream to move through body tissues

When phagocyte encounters something in body tissues that contain antigens –> sends out plasma membrane extensions to engulf foreign body in ENDOCYTOSIS
- hydrolytic enzymes of LYSOSYMES inside phagocyte digest potential invader
[this response is non-specific and hence innate immune response]

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12
Q

Lymphocytes

A

Continuously circulate in bloodstream & contained in
lymphatic system (lymph nodes)

  1. B-lymphocyte [B-cells]
    - produce protein molecules called ANTIBODIES as part of adaptive immune response
    - each type of B-lymphocyte can only synthesise a specific antibody [each antibody is diff bc its produced in response to a diff pathogen]
    - each specific antibody recognises and binds to a specific antigen
  2. ## T-lymphocyte [T-cells]
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13
Q

Antibodies

A

Y-shaped proteins
- at the end of each branch of the Y is a binding site
- binding site is where antibody attaches itself to antigen
- bc antigen is a protein on the surface of a pathogen, antibody attaches to pathogen

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