Diseases of the Immune System Flashcards

1
Q

[type of hypersensitivity reactions]

eosinophils, IL5 from TH2, Antigen binds to IgE on basophils and mast cells
edema, smoothmuscle contraction, mucus production

A

Type 1

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2
Q

[type of hypersensitivity reaction]

Antibodies activate C3a and C5a; functional derangement without evidence of cell or tissue injury

A

Type II

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3
Q

[type of hypersensitivity]

deposition of Ag-Ab complex, inflammation, necrotizing vasculitis, arthus reaction (local)

A

Type III

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4
Q

Granzymes found in CD8 T cell mediate direct killing of antigen by

A

cleaving and activating caspases

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5
Q

Best screening test for SLE

A

ANA

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6
Q

Correlates with disease activity of SLE

A

anti-dsDNA

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7
Q

Specific for SLE

A

anti-smith, anti-dsDNA

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8
Q

[class of lupus nephritis]

Normal LM, ICs in mesangium

A

minimal change disease (Class I)

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9
Q

[class of lupus nephritis]

Messangial cell proliferation, granular mesangial Ig and complement WITHOUT involvement of glomerular capillaries

A

Mesangial proliferative (Class II)

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10
Q

<50% of glomeruli involved, wire-loop appearance, subendothelial IC deposits

A

Focal (Class III)

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11
Q

> /50% of glomeruli involved, wire-loop appearance, subendothelial IC deposits

A

Diffuse (Class IV)

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12
Q

diffuse capillary thickening, subepithelial deposits

A

Membranous (Class V)

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13
Q

Dry eyes, dry mouth, destruction of lacrimal and salivary glands

A

Sjogren Syndrome

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14
Q

Chronic Inflammation, damage to small vessels, rubber hose inflexibility of esophagus, sclerotic atrophy of the skin, thinning of the epidermis, intimal thickening of interlobular arteries

A

Systemic Sclerosis/Scleroderma

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15
Q

Components of CREST syndrome

A
Calcinosis
Reynaud Phenomenon
Esophageal dysmotility
Sclerodactyly
Telangectasia
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16
Q

Autoantibodies in diffuse scleroderma

A

Anti-DNA topoisomerase I

17
Q

[Allorecognition pathway]

Donor Ags presented by recepient APCs to recipient T cells

A

Indirect pathway

18
Q

Occulocutaneous albinism, immunodeficiency, mild bleeding tendency

A

Chediak-Higashi syndrome

o,paored phagolysosome

19
Q

NADPH oxidase deficiency

A

CGD

20
Q

Oral candidiasis, extensive diaper rash, failure to thrive, morbiliform rash due to GVHD; due to adenosine deaminase deficieny

A

SCID

21
Q

Oral candidiasis, extensive diaper rash, failure to thrive, morbiliform rash due to GVHD; due to adenosine deaminase deficieny

A

SCID

22
Q

At 5 to 6 months of age, noted infection H. influenzae, S. pneumoniae, S. aureus, enterovirus, giardia lamblia

A

Bruton aggamoglobinemia

23
Q

Thrombocytopenia, Infections/Immunodeficiency, Eczema

Low IgM, normal IgG, Increased IgA, Increased IgE

A

Wiskott-Aldrich Syndrome

24
Q

HIV initially infects ___ cells

A

dendritic

25
Q

[HIV life cycle]

gp120 binds to ____ during attachment

A

CXCR4 and CCR5

26
Q

[HIV life cycle]

____ is the fusion protein used to integrate itself into host cel

A

gp41

27
Q

apple green bifringence under polarized light

in the spleen, tapioca-like granules (sago spleen); coalesce of deposits: map-like areas (lardaceous spleen)

A

amyloidosis