Other Major Blood Groups Flashcards

1
Q

What genes are prevalent in the Lewis System?

A

Lewis (Le)
Secretor (Se)

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
2
Q

What are Lewis Antigens produced by?

A

Tissue cells
Found in Plasma/Body secretions

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
3
Q

What adds the L-Fuc to the Type 1 precursor?

A

Se gene

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
4
Q

What adds the L-Fuc to the type 2 precursor?

A

H gene

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
5
Q

What is secreted by Le(a+b-)?

A

Lea Antigen

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
6
Q

What secretes A, B, H substances, and is known at the “True Lewis”?

A

Le(a-b+)

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
7
Q

Where do we see a phenotype of Le(a-b-)?

A

Newborn
Cord blood

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
8
Q

When is Lewis detectable and when does the phenotype officially show?

A

Detectable at 10 days of life
Phenotype appears in 6-7 years

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
9
Q

When can the Lewis antigen dramatically decline?

A

Pregnancy

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
10
Q

What is the biological significance of Lewis?

A

Peptic Ulcers
Helicobacter Pylori

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
11
Q

Where do we find the M and N antigens?

A

Glycophorin A (GPA)
Positions 1 and 5

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
12
Q

Where do we find the S and s antigens?

A

Glycophorin B (GPB)

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
13
Q

What can Anti-S and anti-s cause when binding with complement?

A

Severe Hemolytic Transfusion
HDFN

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
14
Q

What can Anti-U cause when it reacts at 37C and binds complement?

A

Severe Hemolytic Transfusion
HDFN

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
15
Q

What can easily destroy MNS antigens?

A

Ficin
Papain
Bromelin
Trypsin (Not S & s)
Chymptrypsin (Not M & N)

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
16
Q

What is synthesized by the sequential action of Glycosyltransferases?

17
Q

What is a common precursor for the P/Globoside Blood group system?

A

Lactosylceramide

18
Q

What is the most common antigen in the P blood group system?

A

P1 Antigen

19
Q

What can inhibit P1?

A

In(lu) type Lu(a-b-)
Rare dominant

20
Q

What can Anti-P1 cause when it reacts at 37C?

A

Immediate/Delayed Hemolytic Transfusion

21
Q

What is another name for Anti-P?

A

Donath-Landsteiner (IgG)
Powerful Biphasic Hemolysin

22
Q

What disease is associated with P and Globoside blood group system?

A

Paroxysmal Cold Hemoglobinuria (PCH)
E. coli

23
Q

What can experience a transient episode of acute abrupt hemolysis?

24
Q

What are the Kell system antigens?

A

Kpa
Kpb
Jsa
Jsb

25
Q

What is a rare silent gene (amorph) referred to as the Kell-null phenotype?

26
Q

Where is the XK gene responsible for Kx protein located?

A

X chromosome

27
Q

How is Kx protein linked to the Kell glycoprotein?

A

Covalently linked

28
Q

What is the third most clinically significant antibody?

A

Anti-K
Detected at 37C and AHG phase

29
Q

Who discovered the weak expression of k, Kpb, and Jsb and what method was used?

A

Allen and coworkers in 1961
Adsorption-Elution methods

30
Q

What can invade red cells because of the role that the Fy gene plays?

A

Plasmodium Vivax

31
Q

What phenotype is resistant to malaria?

A

Fy(a-b-)
Lack of the Fy6 receptor

32
Q

What is well developed at birth and can be destroyed by enzymes like ficin, papain, and bromelin?

A

Fya and Fyb antigens

33
Q

What is Duffy not destroyed by?

A

Neuraminidase
Purified Trypsin

34
Q

What are RBC’s that are Jk(a-b-) resistant to?

35
Q

What enzymes can destroy Kidd antigens?

36
Q

What is clinically significant about Kidd antibodies?

A

Warm Autoimmune Hemolytic Anemia

37
Q

What are the different methods the Lutheran Null Phenotype (a-b-) come about?

A

Dominant InLu suppressor gene
Recessive LuLu gene
Recessive X-linked gene

38
Q

What does Anti-Lua display during testing?

A

Loose, mixed field reaction during in vitro testing