Immunology 2 Flashcards

1
Q

HLA class II structure

A

2 chains (alpha and beta) similar to Ig light chains with transmembrane domain

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2
Q

Clues to Bcell/immunoglobulin defect

A

bacterial infections of respiratory tract

recurrent/persistant Giardiasis

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3
Q

Clues to Tcell defect

A

viral and fungal infections

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4
Q

Phagocytic defects

A

staph infections

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5
Q

Terminal complement defect

A

encapsulated bacterial (Strep. pneumo, Neisseria)

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6
Q

Microlymphocytotoxicity assay

A
To detect HLA class I antigens or antibodies
HLA antisera are incubated with Pt lymphocytes with excess complement and dye (color is + reaction)
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7
Q

mixed lymphocyte culture detects

A

HLA class II diferences

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8
Q

HLA class ___ are 2nd importance only to ABO compatibility in solid organ transplants

A

Class II

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9
Q

mixed lymphocyte culture method

A

dissimilarities in HLA cause proliferation of lymphs

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10
Q

Matching for transplant involes at least

A

A, B, DR

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11
Q

what is mediator of hyperacute rejection

A

HLA abs

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12
Q

transplant crossmatch done by

A

incubating donor lymphos with recipient serum + complement

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13
Q

HLA matching is not as important in which organs

A

heart and lung

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14
Q

Antibodies to protein antigens requres ____ cells

A

Tcells and B cells

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15
Q

antibodies to carbohydrate antigens requires ____ cells

A

B cells only

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16
Q

Most common immunoglobulin defect

A

IgA deficiency

17
Q

Conditions assd with increased IgE

A
parasites,
Churg-Strauss,
Job syndrome,
IgE myeloma,
Hodgkin dz
18
Q

RAST

A

allergen specific IgE measurement (best for inhaled antigens)
not a screening test

19
Q

Delayed type hypersensitivity reaction uses ___ cellls

A

T cells

20
Q

Mitogens used in T cell proliferation assays

A

phytohemagglutinin, concanavalin A

21
Q

severe infection reported in isolated NK cell deficiency

A

herpes virus

22
Q

how to tes for NK cell function

A

chromium release assay

23
Q

nitroblue tetrazolium test

A

<10% cells purple in chronic granulomatous dz (assd with McCloud phenotype/Kx negative)

24
Q

Screening test for classical complement system

A

CH50 (% of Ig-coated sheep red cells lysed by patient serum)

25
Q

Quantitative deficiences of which complement components will decrease CH50

A

C1-9

26
Q

decreased levels of C3 reflect

A

primary C3 deficiency

activation of alternate pathway

27
Q

C4 and C1q levels look at

A

classical pathway

28
Q

which immune defects don’t appear until around 6 months

A

B cell

29
Q

Bruton agammaglobulinemia genetics

A

Atk gene on ChX

30
Q

Testing in Bruton agamma

A

very decreased IgG, decreased circulating B cells, no geminal centers, no plasma cells

31
Q

other conditions assd with Brutons agamma

A

leukemia/lymphoma, autoimmune dz