MIDTERM LECTURE 1: KIDD BLOOD GROUP Flashcards

1
Q

ISBT # of Kidd

A

009

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2
Q

how many antigens does Kidd have

A

3

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3
Q

who discovered Kidd blood group

A

Allen and colleagues, 1951

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4
Q

where was the Kidd antibody first found

A

serum of Mrs. Kidd, whose infant have HDFN

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5
Q

anti-Jka reacted with how many percent of Bostonians

A

77%

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6
Q

antithetical antibody of Jka

A

Jkb

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7
Q

null phenotype of Kidd

A

Jk(a-b-)

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8
Q

when was Jk(a-b-) described

A

1959

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9
Q

Jk3 is present in what individuals

A

have RBCs positive for Jka and Jkb

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10
Q

what happens when Jk(a-b-) individuals receive blood other than Jk(a-b-) donor

A

can cause HTR because of anti-Jk3

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11
Q

T or F:
Jk3 is present in Jka+ and Jkb+ individuals

A

T

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12
Q

why does Jk(a-b-) individuals produce anti-Jk3

A

since they do not have Jka and Jkb= absence of Jk3= Jk3 is foreign

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13
Q

why is Kidd considered as the most notorious blood group

A

cause of delayed HTR

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14
Q

T or F:
Jk antigens are well developed on the RBCs of neonates

A

T

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15
Q

Jka can be detected on fetal RBCs as early as

A

11 weeks

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16
Q

Jkb can be detected on fetal RVCs as early as

A

7 weeks

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17
Q

T or F:
Kidd antigens can cause HDFN

A

T

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18
Q

number of antigen sites per cell of Jk (a+b-)

A

14,000

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19
Q

T or F:
Kidd antigens are very immunogenic

A

F
(not that immunogenic)

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20
Q

T or F:
Kidd antigens can be denatured with enzyme treatment

A

F
(instead, enhanced reactivity with Kidd antibodies)

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21
Q

Kidd antigens can be found in platelets, lymphocytes, monocytes, and granulocytes

A

F

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22
Q

T or F:
Kidd blood group exhibit dosage effect

A

T

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23
Q

T or F:
Jka is more frequently encountered than Jkb

24
Q

What methods can enhance Kidd antibody detection?

A

1) LISS or PEG (promote IgG attachment)
2) Using four drops of serum (increases antibody-antigen ratio)
3) Enzyme treatment (ficin or papain)

25
Q

Can Kidd antibodies bind complement?

A

Yes, many examples do

26
Q

Why is serum preferred over plasma for Kidd antibody detection?

A

Serum allows complement activation, which aids detection.

27
Q

What type of hemolysis is commonly associated with Kidd antibodies?

A

Extravascular, but intravascular can occur in severe cases.

28
Q

Why are Kidd antibodies a common cause of delayed hemolytic transfusion reactions (DHTRs)?

A

Their titers drop quickly, making them hard to detect.

29
Q

What antigen is targeted by all Kidd antibodies?

A

Jk3 (present on Jka+ and Jkb+ RBCs).

30
Q

Are Kidd antibodies usually IgG or IgM?

A

Mostly IgG, but can have an IgM component.

31
Q

On which chromosome is the Jk locus located?

A

Chromosome 18 (18q11-q12)

32
Q

What gene encodes the Kidd blood group system?

33
Q

What is the function of the SLC14A1 gene?

A

It encodes a urea transporter

34
Q

How many exons does the SLC14A1 gene have?

35
Q

What causes the Jka/Jkb polymorphism?

A

An amino acid substitution at position 280

36
Q

Where is the Jka/Jkb polymorphism located on the glycoprotein?

A

On the fourth extracellular loop.

37
Q

Are Jka and Jkb inherited dominantly or codominantly?

A

Codominantly.

38
Q

Which antigens are absent in the Jk(a–b–) phenotype?

A

Jka, Jkb, and Jk3

39
Q

Which populations have the highest occurrence of the Jk(a–b–) phenotype?

A

Polynesians, Filipinos, Indonesians, and Chinese.

40
Q

Has the Jk(a–b–) phenotype been reported in European populations?

A

Yes, in Finnish, French, Swiss, and English families.

41
Q

Which South American indigenous group has reported cases of the Jk(a–b–) phenotype?

A

Mato Grosso Indians of Brazil.

42
Q

What screening method is used to detect Jk(a–b–) RBCs?

A

Delayed lysis in 2M urea.

43
Q

Are there any clinical abnormalities associated with the Jk(a–b–) phenotype?

A

may have defect in urine concentration

44
Q

What do family studies indicate about the inheritance of the Jk(a–b–) phenotype?

A

It is typically homozygous for the silent Jk allele.

45
Q

Why do parents of Jk(a–b–) individuals never type as Jk(a+b+)?

A

Because they inherit JkaJk or JkbJk, leading to a single-dose expression of Jka or Jkb.

46
Q

What dominant gene is associated with the Jk(a–b–) phenotype?

A

In(Jk) (inhibitor gene).

47
Q

T or F:
Individuals with the dominant Jk(a–b–) phenotype produce anti-Jk3.

A

F
(since they still have some Kidd antigens)

48
Q

Dominant type vs recessive type Jk(a-b-)

A

dominant: inheritance of In(Jk) gene
recessive: inheritance of JkJk (silent Jk)

49
Q

What RBCs does anti-Jk3 react with?

A

All Jk(a+) or Jk(b+) RBCs except the autocontrol (since anti-Jk3 is an alloantibody)

50
Q

What type of antibody is anti-Jk3?

A

IgG, reactive in AHG phase

51
Q

How can blood banks confirm suspected anti-Jk3?

A

By antigen typing, since most blood banks lack rare Jk(a–b–) cells.

52
Q

What enhances the reactivity of anti-Jk3?

A

Enzyme pretreatment of RBCs (e.g., ficin, papain).

53
Q

What are two major clinical concerns associated with anti-Jk3?

A

Severe hemolytic transfusion reactions (HTRs) and mild hemolytic disease of the fetus and newborn (HDFN).

54
Q

What type of anemia has been associated with Kidd autoantibodies?

A

Autoimmune hemolytic anemia (AIHA).

55
Q

T or F:
autoantibodies with Kidd specificity are common

56
Q

organisms with Jkb-like specificity

A

Entereococcus faecium
Micrococcus
Proteus mirabilis