Abo blood group _ Amanda Flashcards

1
Q

Landsteiner’s Law

A

“If an antigen is present on the RBC of an individual, the corresponding antibody must be absent in the plasma of that individual and vice-versa.”

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2
Q

Landsteiner’s Law example

A

Individual with A antigen on their RBC, hence blood group A, will have anti-B in their plasma

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3
Q

Where is the ABO locus located?

A

ABO locus located on chromosome 9

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4
Q

What deletion causes a frame shift resulting in the group O phenotype?

A

Deletion at residue 261 causes a frame shift

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5
Q

How many allelic forms does the ABO locus have?

A

3: A, B, and O

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6
Q

What do the A and B alleles each encode?

A

Glycosyltransferase that catalyses the final step in the synthesis of the A and B antigen, respectively

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7
Q

What is the expression of A and B dependent upon?

A

A precursor H substance

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8
Q

What do group O individuals lack?

A

Active enzyme

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9
Q

Where is the H gene (FUT) located?

A

Chromosome 19

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10
Q

What does H gene code for?

A
  • inherited independently
  • codes for an enzyme that converts carbohydrate precursors into H substance
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11
Q

What do the A and B genes code for?

A
  • specific enzymes that convert H substance into A and B antigens
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12
Q

How is the blood group O achieved in an individual?

A

O gene produces an inactive transferase so H substance persists unchanged

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13
Q

Type-1 chain basic precursor for ABH antigens

A

Beta (1-3) linkage

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14
Q

Type- 2 chain basic precursor for ABH antigens

A

Beta (1-4) linkage

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15
Q

What enzyme is involved in the formation of H antigen?

A

L Fucosyl Transferase enzyme (product of H gene)

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16
Q

What enzyme is involved in the formation of the A antigen?

A

N-acetylgalactosaminyl transferase (product of A gene)

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17
Q

What enzyme is involved in the formation of the B antigen?

A

D-galactosyl transferase (product of B gene)

18
Q

Why do Group O invidiuals have more H antigen than the other groups?

A

O gene is a silent allele.
Does not alter the structure of the H substance, so more H antigen sites

19
Q

What is the Bombay phenotype ?

A

Individuals whose RBCs lack the H antigen.
Described as Ohh

20
Q

Why does the Bombay phenotype RBCs also lack A and B antigens?

A

A and B antigens cannot be formed without the H antigen precursor

21
Q

What is the result of the Bombay phenotype?

A

O phenotype- since lack of A and B antigens
Produce anti-H

22
Q

Leucocytes

A

Lymphocytes acquire A, B and H antigens from the plasma of secretors

23
Q

Granulocytes and monocytes

A

Don’t express ABH antigens

24
Q

Platelets

A

Express ABH antigens on glycolipipds and the platelet glycoproteins

25
Q

Where is Blood group O frequency highest and lowest?

A

Highest- Nigeria
Lowest- India

26
Q

Where is Blood group A frequency highest and lowest?

A

Highest- Turkey, Denmark and France
Lowest- Nigeria

27
Q

Where is Blood group B frequency highest and lowest?

A

Highest- Pakistan
Lowest- Australia, Denmark, France and USA

28
Q

Where is Blood group AB frequency highest and lowest?

A

Highest- India
Lowest- Iran

29
Q

Blood group antibodies can be classified into:

A

Non-immune (Naturally occurring)
Immune antibodies
- cold and warm

30
Q

What are naturally occurring antibodies usually?

A

IgM (cold)

31
Q

What are non-immune antibodies

A

-ABO
-Predominantly IgM although some IgG
- produced early in neonatal period following colonisation of gastrointestinal system with bacteria

32
Q

What are immune antibodies?

A
  • develop in response to the incompatible red cells- by transfusion or transplacental passage during pregnancy
  • antibodies commonly IgG, although some IgM
32
Q

What immune antibodies are the only one capable of transplacental passage from mother to foetus?

33
Q

What is an important immune antibody?

A

Rhesus antibodies, especially anti-D

34
Q

What serological methods are used in ABO blood grouping?

A
  • test patient red cells with known antibodies for presence of A or B antigens (cell or forward group)
  • test patient’s serum for presence of Anti A and/or Anti-B antibodies by testing against cells of known red cell phenotype ( serum or reverse group)
35
Q

Molecular typing techniques?

A

Identification of gene sequences on chromosome 9 that confer ABO phenotype
- not widely used currently due to the multiple genetic variations that phenotypically give rise to the A, B, AB and O groups

36
Q

ABO incompatibility

A
  • the rapid intravascular haemolysis which occurs in ABO incompatible transfusions can precipitate severe disseminated coagulation (DIC), prolonged hypotension, acute uraemia, and event death
36
Q

Why are ABO antibodies of major clinical significance?

A
  • naturally occurring and found universally
  • highly reactive, complement activating
  • transfusing a patient with the incorrect ABO blood group may have fatal consequences
  • incompatible donor red cells may be rapidly destroyed by anti-A or anti-B antibody in the recipients plasma
37
Q

What shoul blood grouping and identifying compatible blood components prevent?

A

Adverse transfusion reactions caused by ABO antibodies, however, clerical error can result in the “wrong blood” being transfused into a patient, an error which can result in patient death

38
Q

Serological compatibility testing

A

The patients plasma, containing antibodies, is tested against the red cells of the donor to determine if there is going to be a reaction

39
Q

Electron issue compatibility testing

A
  • for patients who don’t have any history of having red cells antibodies and don’t have any unexpected antibodies in their current plasma sample
  • patients and donors are matched electronically for ABO and RhD with no physical cross match performed
40
Q

Antibody screening - blood group of patient is determined and screened for atypical antibodies

A

If antibody screen positive- crossmatched
If antibody screen negative- electronic issue
If blood is required before cross matching can take place, group O is given