Immunology Flashcards

1
Q

what is the difference between MHC 1 and MHC 2?

A

MHC 1 expressed on all cells - presents to cytotoxic CD* T cells, triggering apoptosis. normally in case of intracellular organisms ie virus, parasites
MHC 2 expressed on APC cells (especially dendritic cells) - present to helper T cells, priming them for further action

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2
Q

which type of cell is the most common antigen presenting cell (APC)?

A

dendritic cell

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3
Q

what are primary vs secondary lymphoid organs?

A

primary - where immune cells deveop/mature (ie thymus, bone marrow)
secondary - where immune cells interact with antigens (ie lymph nodes, spleen)

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4
Q

what are the main subtypes of T helper cells, and which cytokines do they secrete?

A

Th1 - Interferon gamma, IL2
Th2 - secretes IL4, IL5, IL13
Th17 - IL17A, IL17F, IL22

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5
Q

which T helper cell subtype is associated with allergic and parasitic infections?

A

T helper 2

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6
Q

which T helper cell is most likely to be involved in viral infections?

A

TH1

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7
Q

which T helper cell is most likely to be involved in bacterial and fungal infections?

A

TH17

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8
Q

how do T helper cells coordinate an immune response against an infection?

A

through cytokine release

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9
Q

which type of T helper cell secretes interferon gamma?

A

TH1

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10
Q

what is the role of cytokines?

A
  • communicate locally/at a distance
  • recruit more cells
  • coordinate immune cell activity
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11
Q

what are the enzymes used by cytotoxic T cells and NK cells to kill infected cells?

A

perforin

granzyme

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12
Q

what cytokine do NK cells secrete?

A

interferon gamma

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13
Q

what do NK cells do?

A

help kill infected cells if T cell response is not optimal

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14
Q

which type of immunoglobulin does breast milk contain?

A

IgA

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15
Q

what are the physiological changes that occur on the target cell membrane as a result of opsonisation?

A
  • negative charge removed so phagocytes can bind

- increase in number of receptors for phagocytes to bind to

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16
Q

what is the aetiology of primary immunodeficiency diseases?

A

genetic abnormalities (mutations)

17
Q

how can primary immunodeficiency diseases be classified?

A
  • abnormalities in innate immune system
  • abnormalities in lymphocyte development
  • abnormalities in lymphocyte reaction to antigens
18
Q

what is the main primary immunodeficiency disease that results from abnormalities in lymphocyte development?

A

severe combined immunodeficiency (SCID)

19
Q

what types of immunodeficiency disorders are hypogammaglobulinaemia and agammaglobulinaemia?

A

primary immunodeficiencies, resulting from abnormal immune reaction to antigens

20
Q

what is seen is common variable immunodeficiency (CVID)?

A

low levels of IgG

21
Q

what are the three mechanisms by which genetic changes can cause primary immunodeficiency disease?

A
  • single nucleotide polymorphisms
  • mutations
  • polygenic causes
22
Q

how is primary immunodeficiency treated?

A

mild cases - antibiotic prophylaxis

severe cases - immunoglobulin replacement therapy

23
Q

what is the treatment for Severe Combined Immunodeficiency (SCID)?

A
  • stem cell transplant early in life

- gene therapy if no suitable stem cell donor

24
Q

what is the pathology behind SCID?

A

lymphocyte precursors are mutated so don’t respond to growth factors promoting differentiation

25
Q

what’s the acronym that characterises infections seen in immunocompromised patients?

A

SPUR:

serious, persistent, unusual, recurrent

26
Q

what is the common presentation of immunodeficiency caused by abnormalities in antibodies and T cells respectively?

A
  • antibody abnormality: recurrent respiratory infections

- T cell abnormality: serious viral, fungal and intracellular infections