Hypersensitivity Flashcards

1
Q

Type 1 Hypersensitivity

A

Immediate
Mechanism: IgE
Main player: Antibodies
Mechanism of injury: Mast cells and their mediators

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2
Q

Type 2 Hypersensitivity

A

Antibody mediated
Mechanism: IgM, IgG. Against cell surface or ECM antigens
Main player: Antibodies
Mechanism of injury: Opsonization and phagocytosis, complement

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3
Q

Type 3 Hypersensitivity

A

Immune complex mediated
Mechanism: IgM or IgG + antigen
Main player: Antibodies
Mechanism of injury: Complement

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4
Q

Type 4 Hypersensitivity

A

T cell mediated
Mechanism: CD4+ T cells (cytokine-mediated inflammation)
CD8+ T cells (T cell mediated cytolysis)
Main player: T cells
Mechanism of injury: Recruitment and activation of leukocytes

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5
Q

Mast cells activated by cross-linking of ____

A

Fc-epsilon-RI molecules

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6
Q

Lipid mediators of type 1 hypersensitivity

Causes:

A

Prostaglandin D2, Leukotrienes C4, D4, E4

Vasodilation, increased vascular permeability, bronchoconstriction, mucus secretion

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7
Q

Cytokine mediators of type 1 hypersensitivity

Causes:

A

IL-4, IL-5, IL-13

Inflammation/late-phase reaction, IgE production, Eosinophil production/activation

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8
Q

Autoimmune hemolytic anemia

A

IgG against protein antigens on surface of RBCs

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9
Q

Acute Rheumatic Fever

A

Type 2 hypersensitivity
Molecular mimicry
Occurs 2-4 weeks after group A streptococcus pharyngitits

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10
Q

Post-streptococcal glomerulonephritis

A

Type 3 hypersensitivity
Immune complexes in glomeruli trigger inflammation
Occurs after skin or throat infection w/ group A streptococci
Very low serum C3

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11
Q

TH1 produce ____ which leads to ____

A

IFN-gamma

activate macrophages

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12
Q

TH17 produce ____ which leads to ____

A

IL-17

Recruit neutrophils

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13
Q

Poison ivy dermatitis

A

Type 4 hypersensitivity

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14
Q

AIRE gene mutations

A

Failure to delete autoreactive T cells

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15
Q

APECED

A

AIRE gene mutations
Autoimmune PolyEndocrinopathy, Candidiasis, Ectodermal Dystrophy
Hypoparathyroidism, adrenal insufficiency, hypogonadism

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16
Q

FAS gene mutations

A

Impaired apoptosis

17
Q

ALPS

A

FAS gene mutations
Autoimmune LymphoProliferative Syndrome
Hemolytic anemia, thrombocytopenia (low platlets), neutropenia (low neutrophils)
Increased risk of lymphoma

18
Q

FOXP3 gene mutations

A

Impaired regulatory T cells

19
Q

IPEX

A

FOXP3 gene mutations
Immune dysregulation, Polyendocrinopathy, Enteropathy, X-linked
Chronic life-threatening diarrhea due to enteropathy, dermatitis

20
Q

Systemic Lupus Erythematosus

A

Type 3 Hypersensitivity

IC deposition

21
Q

Rheumatoid Arthritis

Cytokines:

A

Type 4 Hypersensitivity
T cell and Abs –> joint inflammation
Innate immune response in synovium
Proinflammatory cytokines: IL-17, TNF, IL-1

22
Q

Diabetes Mellitus Type 1

Inflammation mediated by:

A

Type 4 Hypersensitivity
Immune-mediated destruction of pancreatic beta cells of islets of Langerhans –> insulin deficiency
Mediated by CD4 TH1 cells

23
Q

Myasthenia Gravis

A

Type 2 Hypersensitivity

Abs against acetylcholine receptors at postsynaptic membrane of neuromuscular junction

24
Q

Graves’ Disease

A

Type 2 Hypersensitivity
Hyperthyroidism
Simulated by immune response

25
Q

Hashimoto’s Thyroiditits

A

Hypothyroidism

Autoimmune destruction of thyroid gland