Infection and immunity Flashcards

1
Q

What are the 3 roles of the lymphatic system?

A

Fluid balance
Fluid absorption
Defence

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2
Q

Describe the composition of the lymphatic system

A

The lymph capillaries and vessels

Lymph tissue and organs.

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3
Q

Why are lymph vessels more permeable than blood vessels?

A

They lack a basement membrane.

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4
Q

How do the lymph vessels promote the movement of fluid within them towards the heart?

A

One way semilunar valves,
Thin layer of muscle contained within the wall
Pressure from skeletal muscle contraction.

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5
Q

Describe the lymph drainage into the major veins.

A

Right arm, axillary region, and right side of heart drain into right sub-clavian. The rest of the body drains into the left sub-clavian.

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6
Q

Name the lyphoid organs

A

Lymph nodes, Tonsils, Spleen, Thymus gland

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7
Q

Describe the structure and function of a lymph node.

A

Rounded structures distributed along the lymphatic vessels composed of a cortex and a medulla.
Cortex contains lymphocyte germinal centres and medulla contains the phagocytic macrophages.
Functions include;
Fluid balance- 10% of fluid that leaves the blood returns to the heart via the lymph (3 litres)
Fat absorption- This is via lacteals in the GI tract. The lymph lacks a basement membrane so allows for easy permeability relative to blood vessels. A chyle is lymph milky in appearance from the presence of fat.
Defence- Drainage from sites of inflammation allows APCs to identify any pathogens by the lymphocytes aiding the immune response.

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8
Q

Describe Lymphadenopathy

A

Collective term for all lymph enlargement.
This can be lymphadenitis from infection (painful) or as a SOL due to metastasis from a tumour (firm and usually painless)

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9
Q

Describe the tonsils

A

Small masses of lymphoid tissue around the pharynx. They trap and remove bacteria however congestion with causes tonsillitis.

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10
Q

Describe the spleen

A

Largest lymphoid organ with two main tissue types
Red pulp- Receives Arterial blood and removes old RBCs and recycles the iron though macrophages.
White pulp- Contains T and B cell compartments. Recognise/removes pathogens and activates T and B cells.
It contains a store of blood for in the case of hemorrhagic shock and although its possible to live without a spleen it leaves the body open to certain infections more readily.
Spleen also produces opsonins to enhance phagocytosis and properdin which activates the alternative pathway complement system by binding to and promoting the hydrolysis of C3 into C3a and b.

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11
Q

Describe the thymus

A

Larger in infancy and puberty and shrinks in adults eventually getting fibrosed. Secretes thymosins and is a site of T lymphocyte maturation and production.

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12
Q

What is the role of hepcidin?

A

A chemical mediator that is released from the liver in response to inflammatory markers in the blood. It results in the sequestering of Iron to inhibit bacterial infection growth and proliferation. In chronic inflammation of neoplasia where there is a release of the markers it can lead to anemia of chronic disease.

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13
Q

Define an infection

A

An invasion of a host’s tissues by microorganisms and it can result in a loss of homeostasis of the body by a number of mechanisms i.e mutiplication, host response and toxins.

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14
Q

Provide an example of an intermediary transmission of an infection

A

An individual carrying MRSA on their skin and infecting someone else with it.

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15
Q

How can a patient get infected by a disease they are carrying?

A

Ordinary microbiota/ commensals that have a normal role in the right place. They can cause harm if they go into a new place.

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16
Q

What is horizontal transmission?

A

Contact, inhalation and ingestion.

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17
Q

What is vertical transmission?

A

from mother to child either at or before birth.

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18
Q

what are the 5 stages of an infection getting established in a host

A

exposure, adherence, invasion, multiplication and dissemination. The rate it occurs depends on a number of factors both of the patient and of the pathogens. These are known as virulence factors.

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19
Q

What are the two most significant disease determinants?

A

Pathogen: Virilence factors, size, and antimicrobial resistance.
Patient: Site of infection, comorbidity

20
Q

How do you test for if a patient has an infection?

A

History: symptoms both focal and systemic, severity of and duration of.
Examination: organ specific
Investigations:supportive investigations like FBC, CRP, blood chemistry and imaging and then bacteriology (specimens MCS antigens and nucleic acid detection) and virology.

21
Q

What are the signs of acute inflammation?

A

Focally: Redness, hot, swelling, pain and loss of function.
systemically: fever, elevated WBC levels, increased CRP levels, inflammatory markers in the blood, loss of appetite, sepsis.,

22
Q

Describe the model of an infection?

A

An interplay between the pathogen and the patient. The way they interact is the infection and the severity and management of this infection is what determines the outcome.

23
Q

Describe the types of microbiological agents that can cause disease

A

Prions, virus, bacterium, fungus (yeast mould) and parasite (protozoa, helminth)

24
Q

What are the major patient factors?

A

Age, gender, comorbidities, genetic predisposition, smoking, obesity, social economic state, physiological state, immunosuppression, drugs,

25
Q

What are the major ways that bacteria can be classified?

A

Grain stain (+ve, -ve, acid fast)
Shape.- cocci, baccili, spirochete, and diplo, staph strep,
Aerobic and anerobic
evolutionary routes- archaea and bacterium.

26
Q

What is RSV?

A

Resp syncytial virus.

27
Q

What are the mechanisms of disease spread? examples of each?

A

direct spread- STD.
Inoculation- Hep B, HIV
Haematogenous- endocarditis
Ingestion-C.difficile, helicobacter pylori
Inhalation- TB, chickenpox, norovirus
Vector- malaria, rabies
Vertical transmission- rubella, syphilis, herpes, HIV, cytomegalovirus

28
Q

How does an infection result in host damage?

A

Toxin production and inflammation resulting from interaction with host defences.

29
Q

What are the 3 stages to DDX?

A

History, examination, investigations.

Where is the infection-what is the infection??

30
Q

What are the two types of treatment? examples of each?

A

Specific- antibiotics, surgical drainage and repair

Supportive- symptomatic relief, pain killers, IV fluids, electrolyte input.

31
Q

what is the role of CD3?

A

Required for activation of T cells. Acts as a co receptor in the cell and is activated by phosphorylation.

32
Q

What is the t cell receptor?

A

Molecule that is found on the surface of the t lymphocytes with the role of binding antigens on MHC molecules. Co receptors differ between cells. CD4 on helpers for class 2 MHC and CD8 on cytotoxic t cells for class 1 MHC.

33
Q

What is the role of a CD8 cytotoxic t cell?

A

Role in killing cancer cells, virally infested cells and damaged cells.

34
Q

What are the types of toxins in bacteria?

A

Endotoxins and exotoxins

35
Q

Define immune system

A

Cells and organs that contribute to immune defences against infections and non infectious substances.

36
Q

What are the properties of the innate immune system?

A

instantaneous, non specific, no change in intensity and lack of memory.

37
Q

Describe the barriers that make up the first lines of defence in the body against infections.

A

Physical barriers- skin- impermeable and thick
, mucous membranes (GI tract, respiratory tract and urinary tract.
Mucous and cilia are also part of the physical entrapment and movement process.
Physiological barriers- flushing toxins and bacteria out of the system. Diarrhoea vomit, coughing and sneezing.
Chemical barriers- Low pH (stomach), antimicrobial molecules (IgA, lysozyme, mucous, beta defencins)
Biological barriers- Normal flora to maintain a stable environment which are all non-pathogenic in a normal state.

38
Q

Describe staph aureus

A

c

39
Q

Describe strep pneumoniae

A

c

40
Q

Describe neisseria meningitidis

A

c

41
Q

What is bacteraemia

A

c

42
Q

When can normal flora and commensals become pathogenic?

A

Patient problems- Diabetes, AIDS and immunocompromised, malignant disease, chemotherapy, antibiotics, damage to mucosal surfaces (poor dentition for example), surgical infections into normally aseptic environments.
Breaching of the skin integrity i.e surgery and injections.
Ingestion and UTIs.

43
Q

How do phagocytes recognise pathogens?

A

c

44
Q

How do phagocytes kill pathogens?

A

c

45
Q

What is the role of eosinophils?

A

target multi cellular pathogens.

46
Q

What are PAMPs?

A

c