Common Blood groups Flashcards

1
Q

At what temperature do Duffy antigens optimally react?

A

37°C

The reactive phase for Duffy antigens is typically observed at this temperature using AHG.

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2
Q

What enzymes can destroy Duffy antigens?

A

Papain, ficin, trypsin, bromelain

These enzymes are used in blood typing to assess the presence of Duffy antigens.

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3
Q

What is the frequency of Fy(b) antigen in the Caucasian population?

A

80%

Fy(b) antigen was first identified in 1951 and is prevalent in Caucasians.

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4
Q

What type of antibodies are frequently seen in the Black population concerning the Duffy system?

A

Anti-Fy(a) and Anti-Fy(b)

These antibodies often arise from multi-transfusions and can lead to delayed hemolytic transfusion reactions.

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5
Q

What class of antibodies is associated with the Kidd Blood Group System?

A

IgG

These antibodies are clinically significant and react optimally at 37°C.

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6
Q

What immunoglobulin class is associated with anti-Lu(a)?

A

IgM and IgG

Most examples of anti-Lu(a) are IgM and may occur without prior RBC stimulation.

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7
Q

What is the optimal reaction temperature for anti-Lu(b)?

A

37°C

Most reactions for anti-Lu(b) occur during the indirect antiglobulin test.

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8
Q

What is the main antigen in the P Blood Group System?

A

P1 antigen

The P blood group system also includes Pk and Luke antigens.

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9
Q

What is unique about the P1 and P2 phenotypes?

A

P1 phenotype has both P and P1 antigens; P2 phenotype has P antigen only

80% of individuals with P antigen are P1 phenotype.

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10
Q

What is autoanti-P associated with?

A

Paroxysmal Cold Hemoglobinuria (PCH)

It binds to antigens on the patient’s red cells in cold temperatures and causes hemolysis at 37°C.

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11
Q

What is the Donath-Landsteiner test used for?

A

To confirm the presence of anti-P antibodies

It tests for hemolysis at specific temperatures.

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12
Q

Are I and i antigens antithetical?

A

No

I and i are not antithetical antigens.

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13
Q

Where can I and i antigens be found as soluble glycoprotein Ag’s?

A

In plasma and body secretions

Examples include amniotic fluid and breast milk.

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14
Q

What is the most commonly encountered autoantibody?

A

Anti-I

Using cord cells aids with identification.

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15
Q

What temperature enhances the reactivity of the I autoantibody?

A

Colder temperatures

Testing at 4ºC aids in confirmation of the presence of the antibody.

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16
Q

What is associated with strong autoanti-I?

A

Mycoplasma pneumoniae infections and cold hemagglutinin disease

Anti-i is associated with infectious mononucleosis and lymphoproliferative disease.

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17
Q

What type of antibody is anti-I?

A

IgM

It is poorly developed in infants and is not associated with hemolytic disease of the newborn (HDN).

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18
Q

What happens in reverse grouping when anti-I is present?

A

All results are positive

A1 and B cells always agglutinate, reversing results as group O.

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19
Q

What technique can correct forward typing affected by autoanti-I?

A

Washing cells in warm saline and re-testing

Correcting reverse grouping involves serum prior to testing.

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20
Q

What is anti-IH directed against?

A

Both I antigens and H antigens

It reacts most strongly with group O adult cells.

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21
Q

What are the reactions of Anti-I, Anti-IH, and Anti-H with adult A cells?

A

Anti-I: 2+, Anti-IH: 2+, Anti-H: 0

These reactions vary with other cell types.

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22
Q

Is anti-i clinically significant?

A

No

Auto-anti-i is rare and gives weaker reactions with I RBCs.

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23
Q

What are the serological characteristics of HTLA antibodies?

A

IgG, weak positive to 1+ reactions

They react optimally after 37°C incubation and are inconsistent.

24
Q

Do HTLA antibodies cause hemolytic transfusion reactions?

A

No

They are not clinically significant and may mask clinically significant antibodies.

25
What is a potential issue with HTLA antibodies?
They may mask clinically significant antibodies ## Footnote This is especially relevant in serological testing.
26
How are antibodies classified in blood group systems?
Clinically significant, clinically insignificant, and naturally occurring.
27
What is the significance of amorph (silent) alleles?
They are rare and when inherited, no antigens are made.
28
What is the null phenotype?
Both paired chromosomes possess the same silent allele.
29
What does the term 'high-titre' refer to?
High-titre refers to antibodies that can agglutinate at high dilutions.
30
Fill in the blank: Lewis antigens are _______ and not manufactured by RBCs.
[secreted by tissues].
31
What is the role of secretor genes in the Lewis blood group system?
They help in the formation of Lewis antigens from H structure.
32
What happens to Lewis antigen expression during pregnancy?
Lewis antigen strength may decline due to increased lipoproteins and decreased red cell mass.
33
Describe the inheritance of Lewis antigens.
* Dependent on three sets of independently inherited genes: Lewis genes, Secretor genes, Hh genes.
34
What is the significance of the MNSU blood group system?
* Antigens: M, N, S, s * Clinical significance: Associated with hemolytic transfusion reactions.
35
What are the characteristics of the Kell blood group system?
* Antigens: K, k * Clinical significance: Low-incidence and high-incidence antigens.
36
What is the McLeod Phenotype?
A rare blood group phenotype associated with the Kell system.
37
What is the Duffy blood group system associated with?
Plasmodium vivax resistance.
38
What is the Kidd blood group system known for?
Common cause of delayed hemolytic transfusion reactions (DHTR’s).
39
What type of antibodies are produced by individuals with Le(a-b-) phenotype?
Anti-Le(a).
40
Fill in the blank: The Lewis antibodies are primarily _______.
[IgM].
41
How can Lewis antibodies be neutralized in vitro?
By adding Lewis substance.
42
What is the primary antibody of the Lewis system?
Anti-Le(a).
43
What is the primary antibody produced by individuals with Le(a+b-) phenotype?
Anti-Le(b).
44
Describe the timeline of Lewis antigen development in newborns.
Absent at birth, begins to develop within the first week, and may take up to 6 years for full expression.
45
What is the expected phenotype for most newborns regarding Lewis antigens?
Le(a-b-).
46
How can anti-Lea be neutralized?
By incubating with soluble Lewis substance
47
Who usually produces anti-Lea?
Individuals Le (a–b–) or occasionally Le (a+b–)
48
What are the challenges when identifying Lewis antibodies?
* Agglutination observed at immediate spin, 37°C, and AHG phase * Agglutination is often fragile and easily dispersed
49
What are the M and N alleles?
Co-dominant alleles with antithetical antigens closely linked to S and s antigens
50
What is significant about the U antigen?
It is always present if S or s is present
51
What class is anti-M?
IgM
52
What is the clinical significance of anti-M?
Clinically insignificant, but can react at 37°C and is significant at that temperature
53
What is the frequency of U antigen in the Black population?
Less than 1% are U negative
54
What is the inheritance pattern of the Kell system?
Co-dominant inheritance with three pairs of alleles
55
How is McLeod syndrome inherited?
X-linked inheritance
56
What are common red cell abnormalities in McLeod syndrome?
* Anisocytosis * Acanthocytosis * Reticulocytosis