Immuno Flashcards

(43 cards)

1
Q

HLA A3

A

Hemochromatosis

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2
Q

HLA B27

A

PAIR - Psoriasis, Ankylosing spondylitis, Inflammatory bowel disease, Reiter’s syndrome

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3
Q

HLA DQ2.DQ8

A

Celiac disease

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4
Q

HLA DR2

A

MS, hay fever, SLE, Goodpasture’s

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5
Q

HLA DR3

A

DM Type I, Graves’ disease

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6
Q

HLA DR4

A

DM Type I, RA

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7
Q

HLA DR5

A

Pernicious anemia -> B12 deficiency, Hashimoto’s Thyroiditis

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8
Q

Upper limb/lateral breast

A

axillary nodes

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9
Q

Stomach

A

Celiac nodes

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10
Q

Dudoenum/Jejunum

A

SMA nodes

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11
Q

Sigmoid colon

A

Colic -> IMA nodes

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12
Q

Rectum (lower) and anal canal (above pectinate line)

A

Internal iliac nodes

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13
Q

Anal canal (below pectinate line)

A

Superficial inguinal nodes

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14
Q

Testes/ovaries

A

Paraortic nodes

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15
Q

Scrotum

A

Superficial inguinal nodes

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16
Q

Thigh (superficial)

A

Superficial inguinal nodes

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17
Q

Lateral side of dorsum of foot

A

Popliteal nodes

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18
Q

C3b

19
Q

C3a, C5a

20
Q

C5a

A

neutrophil chemotaxis

21
Q

C5b-C9

A

cytolysis by MAC

22
Q

CD16, CD56

23
Q

CD25, CD3, CD4

A

Regulatory T cells

24
Q

Severe, recurrent pyogenic sinus and respiratory tract infections (S. pneumo, H. influenzae), Inc susceptibility to Type III hypersensitivity (esp. gloerulonephritis)

A

C3 deficiency

25
Defect in BTK (tyrosine kinase) -> no B cell maturation; recurrent bacterial infections after 6 months; dec immunoglobulins of all classes
X-linked (Bruton's) agammaglobulinemia
26
Most common primary immunodeficiency; False-positve beta-hCG due to presence of heterophile Ab; sinopulmonary infections
Selective IgA deficiency
27
Tetany, recurrent vital/fungal infection, congenital and heart and great vessel disease
Thymic aplasia (DiGeorge)
28
Dec TH1 response; disseminated mycobacterial infections, dec IFN-gamma
IL-12 deficiency
29
Eczema, reccurrent staph abscesses, coarse facial features
Hyper-IgE (Job's) - inability of neutrophils to respond to chemotactic stimuli due to TH1 cells failing to produce IFN-gamma
30
Defective IL-2 receptor; adenosine deaminase deficiency; absence of thypic shadow
SCID
31
Failure to thrive, chronic diarrhea, recurrent infections (candida, RSV, VZV, HSV, measles, flu, parainfluenza)
SCID
32
Defects in ATM gene which codes for DNA repair enzymes; cerebellar defects, spider angiomas; IgA deficiency; Inc AFP
Ataxia-Telengectasia
33
Usually defective CD40L on T cells -> inability to class switch; Inc IgM, dec IgG/IgA/IgE; X-linked
Hyper-IgM syndrome
34
WAS gene; T cells unable to reorganize actin cytoskeleton; Inc IgA, dec IgM; X-linked
Wiskott-Aldrich syndrome
35
Thrombocytopenic purpura, Infections, Ezema
Wiskott-Aldrich syndrome
36
Defect in LFA-1 integrin (CD18); recurrent bacterial infections w/ absent pus formationl delayed separation of umbilical cord; neutrophilia
Leukocyte adhesion deficiency (type 1) - neutrophils fail to respond to chemotactic stimuli
37
Defect in lysosomal trafficking regulator gene (LYST); microtubule dysfunction; giant granules in neutrophihls
Chediak-Higashi syndrome
38
Partial albinism, neurological defects, recurrent pyogenic infections
Chediak-Higashi syndrome
39
Lack of NADPH oxidase -> dec reactive oxygen species; inc susceptibility to catalase-positive organisms (S. aureus, E. Coli, Aspergillus, Pseudomonas, Nocardia, Serratia); Abnormal dihydrorhodamine (DHR) flow cytometry test; Negative nitroblue tetrazolium dye test; X-linked
Chronic granulomatous disease
40
CD 14, CD 40, MHC II, B7
Macrophages
41
CD19, CD20, CD21, MHC II, B7
B-cells
42
CD4, CD40L
Helper T cells
43
CD8
Cytotoxic T cells