Blood Bank 4 Flashcards

1
Q

S and s code for the production of which siaglycoprotein?

A

Glycophorein B

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2
Q

All cells that are positive for either S or s are also positive for what antigen?

A

U

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3
Q

What temp doe anti-M most commonly react at?

A

Room temp or below

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4
Q

Anti-M and anti-N characteristics

A

Exhibit dosage

Inhibited by enzymes

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5
Q

Anti-S and anti-s react at what temp

A

37C and AHG

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6
Q

Does enzyme treatment effect reactivity of anti-S or -s

A

Variable effect

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7
Q

Is P1 or P2 more common

A

P1

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8
Q

What antigens do P1 individuals have

A

P1
P
Pk

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9
Q

What antigens do P2 individuals have

A

P

Pk

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10
Q

Which alloantibody, -P or -P1 is more significant for transfusion purposes

A

Anti-P

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11
Q

What autoantibody is known as Donath-Landsteiner antibody

A

Autoanti-P

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12
Q

How does Donath-Landsteiner Ab cause intravascular hemolysis

A

-P binds to RBCs at lower temps in peripheral circulation, activates complement which causes intravascular hemolysis when warmed back to 37C in body core

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13
Q

What disease is Donath-Landsteiner Ab associated with

A

Paroxysmal cold hemoglobinuria

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14
Q

From what is P1 substance made and what does it do

A

Pigeon egg whites

Inhibits P1 antibody reactions

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15
Q

What what temp does anti-LuA and what type of reactivity is seen

A

IS/room temp

Mf pattern of small agglutinates in background of free cells

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16
Q

At what phase does anti-LuB react

A

AHG and 37C

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17
Q

Is LuA high or low frequency

A

Low

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18
Q

Is LuB antigen high or low frequency

A

High

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19
Q

Most significant high frequency Kell antigen

A

k
KpB
JsB

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20
Q

What are the most significant low frequency Kell antigens

A

K
KpA
JsA

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21
Q

McLeod phenotype characteristics

A

Absence of normal XK1 gene
Kx Ag not produced
Kell antigens decreased in amount

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22
Q

McLeod syndrome sometimes associated with what immunodeficiency

A

Type 2 chronic granulomatous disease

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23
Q

K0 phenotype have what antigens

A

High level Kx

Lack all other Kell antigens

24
Q

Antigen second to D in immunogenicity

25
At what phase do K system antigen show up
AHG only
26
What genes influence Lewis phenotype
Le | Se
27
Effect of pregnancy on Lewis antigens
Can cause transient decline
28
Lewis phenotype of leleSese individual
Le(a-b-) | No expression
29
Lewis phenotype of Lelesese individual
Le (a+b+) | LeA only
30
Lewis phenotype of LeleSese individual
Le (a-b+) | LeB only
31
Most common Lewis phenotype
LeB
32
Are Lewis antibodies commonly NRCS
Yes
33
Why do Lewis antibodies not commonly cause HDFN?
Usually IgM Rarely IgG Antigens not well developed at birth
34
What Duffy phenotype are most whites
FyAB (a+b+)
35
What Duffy phenotype are most blacks
Fy (a-b-)
36
Cells with Fy (a-b-) phenotype are resistant to what
Plasmodium vivax infection
37
At what phase do Duffy system antibodies show up
AHG
38
What does enzyme treatment of cells do to reactivity of Fy antibodies
Terminated reactivity
39
At what phase do Kidd antibodies show up
AHG
40
What activity of Kidd allows for detection
Complement binding activity | Causes hemolysis
41
Most common Kidd phenotype in whites
Jk (a+b+)
42
Most common Kidd phenotype in blacks
Jk (a+b-)
43
What trait of Kidd antibodies make them likely to cause HTR
Disappearing act, levels quickly fall to undetectable levels
44
Is I activity stronger in adult or newborn
Adult
45
Is i activity stronger in adult or newborn
Newborn
46
What type of adult has weak expression of I activity and strong expression of i activity and may develop a potent alloanti-I
ii phenotype seen in Japanese individuals
47
Potent autoanti-i capable of causing transient hemolytic anemia is often associated with what disease
Infectious mono
48
What precautions should be taken when transfusing a patient with a potent anti-I or -i
Blood warmer Slower transfusion Keep patient warm
49
What cold reactive alloantibody can group A individuals make which will cause serum to react with all group O cells, but not with group A cells
Anti-IH Must use pre warmed technique Characteristically clumps at IS then goes away
50
What antibodies are inactivated by enzyme treatment
XgA Duffy (Fy) M N
51
Characteristics of anti-XgA
``` Doesn't usually cause HDFN 66% of males 89% of females Usually immune stimulated IgG Detected at AHG Binds complement Doesn't cause in vitro hemolysis ```
52
Type of reactivity seen with anti-SdA
Mixed field pattern of small tightly agglutinated refractile clumps in background of free cells at AHG
53
What can be used to neutralize anti-SdA
SdA substance found in urine
54
Which blood group shows a relationship with the HLA antigens found on young nucleated RBCs
Bg
55
HTLA stands for what
High titer low avidity
56
Chief features of HTLA antibodies
Typically demonstrate weak reactivity that persists even when sera is significantly diluted, Pattern of reactivity at AHG often not reproducible, IgG antibodies may be immune or naturally occurring
57
M and N code for production of which sialoglycoprotein?
Glycophorin A