blood groups Flashcards

(42 cards)

1
Q

Kidd system immunoglobulin type

A

IgG

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2
Q

true or false
the kidd system antigens can bind compliment

A

true
- IgG but can bind

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3
Q

enzyme effect on Kidd system

A

enhanced

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4
Q

Kidd system antigens

A

antithetical: Jka, Jkb
Jk3 present with a or b
-> cells will have Jka/b and 3

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5
Q

Kell system antigens

A

antithetical: K-k, Jsa-Jsb, Kpa-Kpb

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6
Q

frequency of kell system antigens

A

k, Kpb, Jsb: 100
K: 9

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7
Q

frequency of kidd system antignes

A

Jka: 75
Jkb: 75
JK3: 100

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8
Q

duffy system antigens

A

antithetial: Fya-Fyb

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9
Q

duffy system immunoglobulin type

A

IgG

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10
Q

enzyme interaction with duffy system antigens

A

destroyed by enzymes

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11
Q

special characteristics of duffy

A

duffy null prevents vivax entry
syntetic to Rh
- GATA 1 mutation = no duffy on red cells only (no antibodies made)

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12
Q

lutheran system antigens

A
  • Lub: IgG
  • Lua: IgM
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13
Q

chemical interaction with lutheran system

A

destroyed by DTT

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14
Q

special characteristics of lutheran

A

mixed field reactions

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15
Q

P system antigens

A

non antithetical: P1, P, Pk, p (null)

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16
Q

immunoglobulin type of P system

A

IgM -> normally anti P1

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17
Q

special characteristics of P

A

donath-landsteiner
gene codes for galactose transferase

18
Q

MNS system antigens

19
Q

MNS system nulls

A

Mk: whole system
Ena: MNS null but U pos
U: absence of glycophorin B

20
Q

MNS system immunoglobulin type

A

M-N: IgM
S-s: IgG

21
Q

enzyme reaction with MNS system

A

destroyed by enzymes

22
Q

special consideration for MNS

A

dosage, M/N may react into 37 phase (significant), falciparum entry point
-> anti-N made transiently by dialysis patients

23
Q

MNS system frequencys

A

M: 85
N: 70
S: 50
s: 90
U: 100

24
Q

P system frequencies

A

P1: 80
P2: 100
p: 100

25
duffy system frequencies
Fya: 60 Fyb: 75 Fy3: 100
26
lutheran system frequencies
Lua: 5 Lub: 99
27
units to test formula
(100*units needed)/(100-antigen frequency)
28
what is on glycophorin A
- chromosome 4 - attaches M and N on the tail
29
what is on glycophorin B
S or s at the bottom slight N on ends U at base
30
what antigens are present in P1 phenotype
P1, P, Pk w/ no anti-P antibodies
31
describe the action of P1Pk gene
transferase adding galactose to end of sugar of type 2 forms pk antigen - in competition with H fucosyltransferase
32
describe the glob gene
galactosaminyl transferase recognizing two galactoses to add a galnac => P antigen Glob gene on chromosome 3
33
compare I and i
- I: branched, adults - i: linear, fetal
34
describe auto anti-I
- most common cold agglutinin - strong reaction with adults no reaction with fetal cells - enhanced by poly-AHG
35
describe P antibodies
- anti-P1: naturally occurring IgM - anti-P1PL: naturally occuring in Pnull (IgG)
36
what chromosome is Kell located
7
37
Kell null syndrome name
Mcleod - acanthocytes
38
role of XK
XK multipass protein with KX antigen
39
describe big I
internal portion of type 2 chains branchy, adult form related to M. pneumonia
40
describe little i
in infants, linear i related to infectious mono
41
describe anti-I
auto-anti-I causing cold agglutination -> agglutinates only with m. pneumonia infection, otherwise undetectable
42
describe anti-i
in infants after infectious mono infection