Immunology Flashcards

(33 cards)

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
measurement of complement
functional assessment of pathways with functional assays for genetic deficiencies
26
allograft?
transfer between genetically non identical members of the same species
27
xenograft
transfer between species
28
GVHD?
graft versus host disease
29
prevention of graft rejection?
ABO matching Close tissue matching - Class 1 and 2 HLA: especially HLA-A, HLA-B & HLA-DR loci prophylactic immunosuppressive therapy
30
GVHD path
principally occurs with bone marrow transplantation - due to: - presence of functioning immunocompetent donor T cells in the graft - HLA differences
31
early signs of GVHD?
erythematous rash on hands and soles of feet - significant diarrhoea
32
current immunotherapies three main groups
immunosuppressive/immunomodulatory drugs, alternatives to drug therapy and immunoglobulin therapy
33
examples of immunosuppressive drugs
steroids in combination with Azathioprine and Cyclophosphamide