Immune System Flashcards

(29 cards)

1
Q

Most potent eosinophil activating cytokine

A

IL-5

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2
Q

Opsonization complement in type 2 hypersensitivity

A

C3b

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3
Q

Inflammation complement in type 2 hypersensitivity

A

C3a and C5a

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4
Q

Common tissues involved in Type III Hypersensitivity

A

Kidneys
Joints
Small blood vessels

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5
Q

CD8 cell action in type IV hypersensitivity is through

A

Perforins

Granzymes- cleave and activate caspases

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6
Q

Accumulation of mononuclear cells, mainly CD4 and macrophages around venules, producing perivascular “cuffing”

A

Tuberculin reaction

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7
Q

Best screening test for SLE

A

ANA antibody

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8
Q

Specific for SLE antibodies

A

Anti -Smith

Anti- dsDNA

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9
Q

Lupus nephritis type where there is swelling and hypercellularity
Affecting <50% of glomeruli

A

Focal (Class 3)

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10
Q

Lupus nephritis class where there is wire loop appearance of capillaries and >50% glomeruli affected

A

Diffuse (Class 4)

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11
Q

Lupus nephritis class where there is >90% sclerosis of glomeuli

A

Advanced sclerosing (Class 6)

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12
Q

Drug induced lupus is associated with anti histone antibodies and these drugs

A

Hydralazine
INH
Procainamide
D-Penicillamine

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13
Q

Dry eyes
Dry mouth
Autoimmune destruction of lacrimal and salivary glands

A

Sjogren

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14
Q

Diagnosis for Sjogren syndrome

A

Lip biopsy

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15
Q

Most important and most common autoantibodies detected in Sjogren

A

Anti Ro and Anti La

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16
Q

Triad of Scleroderma

A

Chronic inflammation
Widespread damage to small blood vessels
Progressive interstitial and perivascular fibrosis in the skin and multiple organs

17
Q

CREST syndrome of Scleroderma

A
Calcinosis
Raynaud phenomenon
Esophageal dysmotility
Sclerodactyly
Telangiectasia
18
Q

Autoantibodies in diffuse scleroderma

A

Anti DNA topoisomerase I (anti-scl 70)

19
Q

Autoantibodies in limited scleroderma

A

Anti centromere

20
Q

Most common antibody associated with scleroderma renal crisis

A

Anti-RNA pol III

21
Q

Most common extracutaneous manifestation of scleroderma

A

Raynaud phenomenon

22
Q

Most common cause of death in scleroderma

A

Interstitial lung disease and pulmonary arterial hypertension

23
Q

Most commonly seen in both limited and diffuse cutaneous scleroderma

A

Skin involvement

Raynaud phenomenon

24
Q

Autoantibody in mixed connective tissue disease

A

Anti-RNP particle containing U1 RNP

25
Presentation of mixed connective tissue disease
Synovitis of the fingers Raynaud phenomenon Mild myositis
26
Usual organs affected in Graft vs Host disease
Skin GIT HBT Immune system
27
``` X linked recessive Btk gene defect No B cell development Symptoms at 5-6 months of life Absent germinal centers and plasma cells Infections of respiratory tract, viral, Giardia lamblia ```
Bruton X agammaglobulinemia
28
Treatment for Bruton agammaglobulinemia
Immunoglobulin replacement
29
X linked disturbance of early T lymphocyte development
Severe combined immunodeficiency