Disease Challenges and Strategies Flashcards

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1
Q

How was disease brought about?

A

> Europeans brought disease such as a wave of epidemic diseases including smallpox, typhoid, pneumonia, whooping cough etc.
Many of the europeans colonist populations had resistance to diseases like measles, scarlet fever as thy already had been exposed to the responsible pathogens before coming to Australia.
However, these diseases spread rapidly through and annihilated those who hadn’t been exposed to it before.

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2
Q

Diet?

A

> There was restricted access to traditional foods, rationing was imposed ( low quality and quantity of foods)
Aboriginal people where forced to adapt to European style of high sugar and flour based diet

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3
Q

Lifestyle?

A

> Nomadic life morphed into a more stationary lifestyle
As Aboriginal people lived in one place = to an increased exposure to an increased spread of pathogens

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4
Q

Pathogen

A

A disease causing organism

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5
Q

Infection

A

Occurs when a pathogen has breached the first line of defence and has started to replicate within the host

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6
Q

Disease

A

Is the consequence of the pathogen’s invasion causing damage and impacting on the normal function of the body’s tissues

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7
Q

Virulence

A

The likelihood that a pathogen, once it is in the body, will cause disease and harm to the host

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8
Q

Contagious

A

Is the likelihood that the pathogen will spread between individuals

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9
Q

Emerging Disease

A

A disease that has occurred in humans before, or has occurred previously, but affected only a small number of people.
E.g. HIV infections, west nile virus, lyme disease, ebola.

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10
Q

Re-emerging disease

A

A disease that was once present and had a dramatic decline in case numbers, but has returned and is affecting a significant proportion of the population.
E.g. Influenza, malaria, tuberculosis.

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11
Q

Contributing factors to emergency of disease is human behaviour

A

> Population growth, travel, poverty, ecological damage, food supply chains, intensive farming and climate change

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12
Q

2 reasons for a disease to re-emerge

A

> Resistance/ Evolution of a pathogen
Drop of vaccination numbers

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13
Q

Resistance

A

Bacteria can either mutate or exchange genetic material with other bacteria of the same or different species.

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14
Q

Mutations

A

Mutations of bacterial genes could result in the bacteria being able to:
> Prevent drugs from adhering to their surface
> Decrease the permeability of their plasma membrane to drugs
> Actively pump out the drug
> Use enzymes that destroy the action of the drug

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15
Q

Exchange of Genetic Material

A

> Conjugation is one way in which genetic material is exchanged between bacteria.
Involves the pilus from one bacterium extending and joining that of another bacterium, forming a bridge enabling the plasmid DNA to be exchanged between the two bacteria.
The plasmid could then contain a gene that increases the bacterium’s ability to survive medications.
The widespread use of antibiotics is acting as a selection pressure driving the evolution of stronger and more resistant pathogens.

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16
Q

Differences between endemic, epidemic and pandemic

A

> Classification due to rate of spread, not severity.
Endemic: Transmission occur, but the number of cases remain constant
Epidemic: The number of cases increases
Pandemic: When the epidemic occur at several continents (global epidemic)

17
Q

Endemic

A

> Similar to a pandemic due to its contagiousness and longevity
Contained to a specific geographical area
More predictable and therefore easier to manage

18
Q

Epidemic

A

> An unexpected increase in the number of disease cases in a specific geographical area. Disease in this context doesn’t always pertain to a contagious illness

19
Q

Pandemic

A

> When the growth rate of a particular disease or sickness is considered exponential.
Spread across many countries

20
Q

Immunotherapy

A

> Is a treatment for a disease that causes the activation or suppression of the immune system.
The main types of immunotherapy include:
- Monoclonal antibodies (mAbs)
- Non-specific immunotherapies
- Cancer vaccines

21
Q

Monoclonal Antibodies

A

Are made in the laboratory to work in the same way that naturally produced antibodies respond during the adaptive immune response.
There are numerous types and can be made to target a variety of cells and substances.

22
Q

Two types of mAbs

A

> Bispecific mAbs: Attach to target cells to signal for an immune response. Is laboratory made with two different antigen-binding sites, so it can attach to two different antigens at one time.

> Conjugated mAbs: Deliver a cytotoxic or radioactive ‘payload’ directly to the target cell. Is one that has been combined with a chemotherapy drug (a cytotoxin) or radioactive substance.
Can therefore be used to deliver the drug or radioactive substance directly to the cancerous cells, preventing their growth and lessening the damage to healthy cells in the area.

23
Q

Autoimmune Disease

A

> Are a malfunction of the immune system.
Using drugs against the malfunctioning cells is difficult due to the risk of weakening the immune response so much that it allows pathogens to take hold.
Treatments should specifically target only the malfunctioning cells or molecules of the immune system, not the whole system.

24
Q

Multiple Sclerosis

A

Occurs when a person’s own immune cells attack the central nervous system, resulting in damage to the insulating myelin sheath of nerve cells.

Ocrelizumab is the first approved monoclonal antibody treatment for a type of multiple sclerosis.
Ocrelizumab targets the CD20 receptor of B cells.
Reduced the attacks by the immune cells on the central nervous system.

25
Q

Allergic Reactions

A

Another example is the use of mAbs to inhibit IgE antibodies involved in moderate to severe allergic reactions.

26
Q

Sources of protein that makes up mAbs

A

> Murine: Made of mouse proteins
Chimeric: A mixture of mouse and human proteins
Humanised: Mouse Protein attached to predominantly human proteins
Transgenic: Fully human proteins produced with the use of transgenic mice

27
Q

How to make mAbs

A

> The first mAbs were mouse mAbs.
So not to be rejected by humans (as mouse mAbs would be considered non-self), researchers used recombinant DNA techniques to produce chimeric, humanised and transgenic mAbs.