AAW - Immunology Flashcards

1
Q

In lymph tissue, where is the site of B-cell localization and proliferation?

A

Follicle of cortex of lymph node.

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2
Q

What types of cells are in the Medullary sinuses of lymph nodes?

A

Reticular cells and macrophages

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3
Q

Lymph drainage:
What lymph node cluster drains the:

Lower rectum to anal canal (above pectinate line), bladder, vagina (middle third), prostate

A

Internal iliac

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4
Q

Lymph drainage:
What lymph node cluster drains the:

Testes, ovaries, kidneys, uterus

A

Para-aortic

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5
Q

Lymph drainage:
What lymph node cluster drains the:

Anal canal (below pectinate line), skin below umbilicus (except popliteal territory)

A

Superficial inguinal

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6
Q

What drains everything besides the right side of the body above the diaphragm, and where does it drain to?

A

The thoracic duct - drains into junction of left subclavian and internal jugular veins

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7
Q

Histological hallmark of the sinusoids of the spleen

A

Long, vascular channels in red pulp (made of RBCs) with fenestrated “barrel hoop” basement membrane.

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8
Q

What type of cells are found in the periarterial lymphatic sheath of the white pulp of the spleen

A

T cells

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9
Q

What type of cells are found in the follicles within the white pulp of the spleen

A

B cells

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10
Q

What types of cells are found in the marginal zone of the spleen

A

Antigen presenting cells (APC) - macrophages and specialized B cells that capture blood borne antigens

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11
Q

If you have a splenic dysfunction, what infectious organisms are you more susceptible to?

A

Encapsulated organisms:

SHiNE SKiS

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12
Q

What types of cells are in the following areas of the Thymus:

cortex
medulla
Hassal corpuscles

A

Cortex - immature T cells

Medulla - mature T cells

Hassall corpuscles - epithelial reticular cells.

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13
Q

calcineurin inhibitors

name 2
mech
particularly high yield toxicity

A

cyclosporine, tacrolimus

cycloSPORKin TACKrolimus

2 things that stab you

Blocks IL-2 transcription, inhibiting T cells

Nephrotoxic, because when you shank someone you go for the kindeys

also tacroLIMEus and siroLIMEus both bind FKBP (when you get stabbed and put a LIME on it, it hurts and you say FucK)

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14
Q

what is the first test you do to screen for HIV

A

enzyme linked immunosorbent assay to test for antibodies against HIV proteins

the patient could have a false negative until 3-7 weeks after getting HIV

confirm with western blot (AKA checking the viral load)

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15
Q

adult male with random and sudden hemoptysis, elevated creatine and BUN, hematuria

A

goodpastures, autoantibodies against type IV collagen (in pulmonary alveoli and renal glomeruli)

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16
Q

young person has recurrent bacterial and fungal infections with staph, e.coli. and aspergillus

what disease
what cytokine can you give them

A

CGD (chronic granulomatous disease)

lack of NADPH oxidase activity, phagocytes use NADPH oxidase to convert molecular oxygen to ROS

susceptible to catalase positive organisms

give the recombinant cytokine INF-gamma

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17
Q

nitroblue tetrazolium test

A

determines phagocyte NADPH oxidase activity, which is reduced in patients with CGD

phagocytes use NADPH oxidase to convert molecular oxygen to ROS

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18
Q

severe pyogenic infections early in life; opportunistic infection with pneumocystis, cryptosporidium, cmv

increased serum IgM

what is the mech

A

hyper-IgM syndrome:

Most commonly due to
defective CD40L on Th
cells = class switching defect (you can only make IgM);
X-linked recessive.

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19
Q

chronic granulomatous disease - what orgs are you susceptable to?

what is the molecular defect

A
susceptibility to catalase
\+ organisms (PLACESS):
Pseudomonas, Listeria,
Aspergillus, Candida, E. coli,
S. aureus, Serratia.
Defect of NADPH oxidase
decrease in reactive oxygen species
(e.g., superoxide) and
absent respiratory burst
in neutrophils; X-linked
recessive.
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20
Q

HLA-A3

A

hemochromatosis

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21
Q

HLA-B27

A

PAIR

Psoriatic arthritis, Ankylosing spondylitis, arthritis of Inflammatory bowel disease, Reactive arthritis

AKA the seronegative arthropathies

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22
Q

HLA-DQ2/DQ8

A

celiac disease

started going to Dairy queen when I was 2 but had to stop when I was * because they found out i have celiac

23
Q

HLA-DR2

A

multiple sclerosis, hay fever, (2,3,SLE) SLE, Goodpasture syndrome

an MS2 student in a HAY PASTURE with BUTTERFLIES (SLE)

24
Q

HLA-DR3

A

diabetes mellitus type 1, (2,3,SLE) SLE, Graves disease, hashimoto, addison

Addison got recently added to DR3 and 4

hashimoto recently got added to DR3

25
Q

HLA-DR4

A

Rheumatoid arthritis (4 walls in a RHEUM), diabetes mellitus type 1, addison disease

addison got recently added to DR3 and DR4

26
Q

HLA-DR5

A

pernicious anemia –> vit b12 deficiency, Hashimoto thyroiditis (i got five on that hash - and hash is pernicious)

27
Q

anti-ach receptor antibody

A

myasthenia gravis

28
Q

anti-basement membrane antibody

A

goodpasture syndrome (type 4 collagen)

29
Q

anticardiolipin antibody

A

SLE

30
Q

anticentromere antibody

A

limited scleroderma (CREST):

calcinosis and centromere, Raynaud’s, esophageal dysmotility, sclerodactyly, telangiectasia.

31
Q

anti-desmoglein antibody

A

pemphigus vulgaris

32
Q

anti-glutamic acid decarboxylase antibody

A

AKA GAD-65

type 1 diabetes mellitus

33
Q

antihemidesmosome antibody

A

bullous pemphigoid

34
Q

anti-histone antibodies

A

drug-induced lupus

35
Q

anti-Jo, anti-SRP, anti-Mi2

A

polymyositis, dermatomyositis

36
Q

antimicrosomal antibodies

A

hashimotos with antithyroglobulin

37
Q

antimitochondrial antibodies

A

primary biliary cirrhosis

38
Q

antinuclear antibodies

A

SLE, but not specific (used just for screening)

39
Q

antiparietal cell antibodies

A

pernicious anemia

40
Q

antiphospholipase A2 receptor

A

primary membranous nephropathy - granular immune complex deposition, nephrotic syndrome, spike and dome appearance with subepithelial deposits

(glucocorticoids inhibit phospholipase A2, which converts phospholipids to arachidonic acid)

41
Q

anti-dna topoisomerase I antibodies

A

diffuse scleroderma (antibody is also known as anti-scl-70)

42
Q

anti-smooth muscle antibodies

A

autoimmune hepatitis type 1

43
Q

anti-SSA, anti-SSB (anti-Ro, anti-La) antibodies

A

sjogren syndrome

44
Q

anti-U1 RNP antibodies

A

mixed connective tissue disease - features of SLE, systemic sclerosis, and polymyositis

antibodies are related to the anti spliceosomal snRNP antibodies (aka anti smith) seen in SLE

45
Q

voltage-gated calcium channel antibodies

A

lambert-eaton syndrome

46
Q

IgA anti-endomysial, IgA anti-tissue transglutaminase

A

celiac disease

47
Q

MPO-ANCA/p-ANCA antibodies

A

microscopic oplyangiitis, eosinophilic granulomatosis with polyangitis (churg-strauss)

48
Q

PR3-ANCA, c-ANCA

A

granulomatosis with polyangitis (wegeners)

49
Q

autoantibody in Rheumatoid arthritis

A

IgM antibody that targets IgG Fc region (Rheumatoid factor)

also anti-CCP (more specific)

50
Q

snRNP antibody

A

AKA anti-smith antibody

SLE

51
Q

3 things that are s-100 positive

A

langerhans histiocytosis

melanoma

schwannoma

52
Q

where are T cells found in a lymphnode?

b cells?

A

t - paracortex

b - follicles

53
Q

catch-22

A
Cleft palate
Abnormal facies
Thymic aplasia
Cardiac defects
Hypocalcemia secondary to parathyroid aplasia

22q11 microdelesion leads to digeorge syndrome (thymic, parathyroid, and cardiac defects)

and velocardiofacial syndrome (palate, facial, and cardiac defects)