Immunology Flashcards

1
Q

HLA class 1 presents to

A

CD8 - cytotoxic T cells

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2
Q

HLA class 2 presents to

A

CD4 - helper T cells

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3
Q

hypersensivity

A

immune response is exaggerated or inappropriate to harmless environmental antigens

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4
Q

Ab in type 1 hypersensitivity, also called?

A

IgE

also called allergy and atopy

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5
Q

allergy is a result of

A

end result of complex interplay of a number of factors - atopy, environment, immune reactivity

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6
Q

pathogenesis of allergy

A

mast cells + IgE - stimulate mediators to cause secretions, vasodilation, mucosal oedema

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7
Q

diagnosis of allergy

A

hx , ex, skin prick tests

IgE (RAST test)

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8
Q

type 2 hypersensitivity

A

IgG.or IgM

self or exogenous stimulator

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9
Q

examples of type 2 self hypersensitivity

A

graves
myasthenia gravis
goodpastures

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10
Q

examples of type 2 exogenous hypersensitivity

A

blood transfusion - haemolytic reaction

HDN

hyper acute graft rejection

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11
Q

type 3 hypersensitivity

A

antibody antigen complex disposition in tissues = immune complex recruits inflammatory cells - tissue damage

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12
Q

two outcomes from hypersensitivity type 3

A

serum sickness

arthrus reaction

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13
Q

serum sickness?

A

systemic illness where immune complexes form in the circulation and are deposited in a widespread fashion throughout many tissues

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14
Q

arthrus reaction

A

a more localised disorder where complexes are actually formed locally in tissues rather being deposited from the blood

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15
Q

e.g. of Hypersensitivity 3

A

EAA
post strep GN
SLE

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16
Q

type IV hypersensitivity mediated by

A

T helper cell mediated and its cytokine products IL2 , gamma interferon

17
Q

type 4 examples

A

Mantoux test

contact dermatitis

18
Q

autoimmunity due to

A

loss of tolerance - therefore autoreactive T and B cells are able to mature

19
Q

primary defects of innate immunity

A

chronic granulomatous disease: problem with intracellular killing

leucocyte adhesion def (LAD): neutrophils unable to attach to endothelium

20
Q

complement deficiencies?

C1-c4?

C3?

C5-C9?

A

C1-C4: immune complex disease, infection (strep, haemophilia, meningococcus)

C3: recurrent above infections

C5-C9: recurrent neisserial infection

21
Q

hereditary angioedema

A

similar presentation to anaphylaxis - but not itchy, or painful

deficiency of C1 inhibitor (control protein)

tx - infusion of C1 inhibitor

22
Q

SCID?

A

severe combined immune deficiency

dysfunction with T AND B cells

23
Q

SCID pc?

A

well for first 3 months

persistent superficial candida

diarrhoea and failure to thrive

then cross line –> chronic bronchitis, interstitial pneumonitis, bacterial seps

24
Q

TX for SCID

A

supportive until suitable bone marrow donor

earlier the better

25
Q

measurement of complement

A

functional assessment of pathways with functional assays for genetic deficiencies

26
Q

allograft?

A

transfer between genetically non identical members of the same species

27
Q

xenograft

A

transfer between species

28
Q

GVHD?

A

graft versus host disease

29
Q

prevention of graft rejection?

A

ABO matching
Close tissue matching - Class 1 and 2 HLA: especially HLA-A, HLA-B & HLA-DR loci

prophylactic immunosuppressive therapy

30
Q

GVHD path

A

principally occurs with bone marrow transplantation - due to:
- presence of functioning immunocompetent donor T cells in the graft

  • HLA differences
31
Q

early signs of GVHD?

A

erythematous rash on hands and soles of feet - significant diarrhoea

32
Q

current immunotherapies three main groups

A

immunosuppressive/immunomodulatory drugs, alternatives to drug therapy and immunoglobulin therapy

33
Q

examples of immunosuppressive drugs

A

steroids in combination with Azathioprine and Cyclophosphamide