Immunology Flashcards

1
Q

site of fluid absorption and entrance for circulating lymphocytes to the node

A

high endothelial venules
endothelial cells have signals for antigen carrying cells:
• T cells remain in the deep cortex
• B cells migrate to the nodular cortex

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2
Q

embryologic derivation of the thymus

A

3rd and 4th pharyngeal pouches

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3
Q

distinguishing feature of the thymic medulla

A

Hassall corpuscle
contains mature T cells
keratinized center

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4
Q

part of the spleen that filters blood and contains macrophages for removal of RBCs

A

red pulp

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5
Q

Within the spaces of the bone, medullary cavity of young long bones and spaces of spongy bone

A

red bone marrow

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6
Q

Bone marrow not active in blood cell formation contains adipose cells giving it the appearance of adipose tissue

A

yellow bone marrow

present in the medullary cavity in adults

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7
Q

mediated by molecules in the blood and mucosal secretions (antibodies) produced by B lymphocytes. Principal defense mechanism against extracellular microbes & their toxins

A

humoral immunity

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8
Q

Innate or adaptive?

lysozyme, complement, CRP, mucus, defensins

A

innate immunity

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9
Q

LPS, flagellin, ssRNA

A

PAMPs = pathogen-associated molecular patterns

recognized by TLRs

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10
Q

encoded for by the HLA genes

A

MHC

these present antigen to T cells and bind TCRs (CD3)

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11
Q

loci for MHC I
expressed on all nucleated cells
present endogenously synthesized antigens (from inside the cell -> so recognizes self)

A

HLA: A, B & C

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12
Q

loci for MHC II
Expressed ONLY on APCs
presents exogenously synthesized proteins (ex from bacteria & viral capsids)

A

HLA: DR, DP, DQ

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13
Q
HLA subtype associated with PAIR diseases:(seronegative arthropathies)
Psoriatic arthritis
Ankylosing spondylitis
Inflammatory Bowel Disease arthritis
Reactive arthritis (Reiter syndrome)
A

B27

the B27 has a “pair” of engines on each wing

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14
Q

HLA subtype associated with hemochromatosis

A

A3

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15
Q

HLA subtypes associated with celiac disease

A

DQ2/DQ8

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16
Q
HLA subtype associated with:
Multiple sclerosis
hay fever
SLE
Goodpasture
A

DR2

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17
Q

HLA subtype associated with:
type I DM
SLE
Graves disease

A

DR3

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18
Q

HLA subtype associated with:
DM type 1
Rheumatoid arthritis

A

DR4

a “rheum” has 4 walls”

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19
Q

HLA subtype associated with:
pernicious anemia
Hashimoto thyroiditis

20
Q

cell that responds to absence of MHC I

A

NK

use perforin & granzymes to induce apoptosis of virally infected cells and tumor cells

21
Q

T cell that directly kills virally-infected cells
Delayed type hypersensitivity (Type IV)
Acute & chronic organ rejection

22
Q

TCRs express high affinity for self antigens & undergo apoptosis

A

Negative selection -> occurs in the medulla of the thymus

Positive selection occurs in the cortex and is the survival of T cells that have TCRs that can bind self MHC

23
Q

signal 2 of T cell activation

A

dendritic B7 and naive T cell CD28

24
Q

helps deliver granule contents of CTL to target cell

25
produces IL-10 and TGF-beta (anti-inflammatory cytokines)
T regs
26
immunoglobulins that fix complement
IgG and IgM
27
binds mast cells and basophils cross-links when exposed to allergen & mediates type I hypersensitivity through release of histamine & other inflammatory mediators
IgE
28
Acute phase reactants produced by the liver in both acute and chronic inflammatory states. Induced by IL-6, IL-1, TNF-alpha, IFN-gamma
``` serum amyloid A CRP -> opsonin ferritin fibrinogen -> correlates with ESR hepcidin -> prevents iron release from ferritin -> anemia of chronic disease ```
29
complement pathway activated by microbe surface molecules
alternative pathway
30
complement pathway mediated by IgG and IgM
classic pathway | "GM makes classic cars"
31
complement proteins of anaphylaxis
C3a, C4a, C5a
32
complement component for neutrophil chemotaxis
C5a
33
complement opsonin
C3b | "C3b binds bacteria"
34
MAC
C5b-9
35
prevent complement activation on self cells
DAF (CD55) and C1 esterase inhibitor
36
deficiency causes complement-mediated lysis of RBCs & paroxysmal nocturnal hemoglobinuria
DAF
37
deficiency causes hereditary angioedema
C1 esterase inhibitor
38
increases susceptibility to recurrent Neisseria infections
C5-C9 deficiency
39
increases susceptibility to recurrent pyogenic sinus and resp tract infections, as well as type III hypersensitivity
C3 deficiency
40
activates NK cells to kill virus-infected cells
IFN-gamma
41
``` enhances class switching to IgA growth & differentiation of eosinophils ```
IL-5
42
cytokine chemotactic for neutrophils
IL-8
43
Which cells do not have MHC I?
Red blood cells. All others do
44
MHC I molecule composition
Heavy chain & beta2 microglobulin | MHC I presents foreign antigen to cd8 T cells
45
Enzyme specific to mast cell and is elevated in drug hypersensitivity
Tryptase
46
Recurrent otitis media, sinusitis, bronchitis and GI infections Transfusion with blood products can cause fatal anaphylaxis
Selective IgA deficiency | Form IgG antibodies to IgA