Week 8 Flashcards

ANTIBODY IDENTIFICATION - ADDITIONAL SPECIAL TECHNIQUES

1
Q

What is the clinical significance of cold antibodies?

A

Cold antibodies are usually clinically insignificant and do not cause red cell destruction.

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2
Q

Why are cold antibodies significant in testing?

A

They interfere with testing intended to detect significant antibodies.

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3
Q

At which temperatures are cold (IgM) antibodies typically present?

A

Cold antibodies are typically present at IS (Immediate Spin), RT (Room Temperature), and sometimes at 37°C.

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4
Q

What type of reactions can cold antibodies show on MTS gel cards?

A

Cold antibodies can show mixed field reactions on MTS gel cards.

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5
Q

How can weak reactions of cold antibodies on a panel be enhanced?

A

By incubating the panel at or below room temperature, sometimes at 4°C in a fridge.

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6
Q

What does a positive DAT indicate in the context of cold antibodies?

A

It indicates that patient cells are reacting with patient plasma in vivo.

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7
Q

What is the next step if polyspecific testing is positive for cold antibodies?

A

The next step is to differentiate between IgG and C3.

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8
Q

What kind of reaction strength is commonly observed across the cell panel in cold antibody testing?

A

Non-specific reactions or phases with fairly consistent reaction strengths.

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9
Q

What technique might be used if cold antibodies are causing confusion in test results?

A

The absorption technique may be used to try and remove the antibody.

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10
Q

How can cold antibodies lead to ABO discrepancies, and in which blood group is this not typically seen?

A

Cold antibodies can cause ABO discrepancies, but this is not typically seen in Group O patients.

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11
Q

What medical conditions are often associated with patients who have cold antibodies?

A

Mild anemia, Mycoplasma pneumonia infection, or infectious mononucleosis.

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12
Q

What technique might be required in crossmatching blood for patients with cold antibodies?

A

A prewarm technique may be required.

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13
Q

What class of antibodies does the Ii blood group system belong to, and what is its optimal reaction phase?

A

It belongs to Class IgM, with an optimal reaction phase at room temperature.

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14
Q

Where is the i antigen expressed in the Ii blood group system?

A

The i antigen is expressed on newborn cells and cord blood cells.

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15
Q

Over what period does the i antigen convert to the I antigen structure in the Ii blood group system?

A

The i antigen converts to the I antigen structure over a 2-year period.

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16
Q

Where is the I antigen expressed in the Ii blood group system?

A

The I antigen is expressed on adult cells.

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17
Q

What type of antibody is Anti-I and when does it show optimal reactivity?

A

Anti-I is a common autoantibody with optimal reactivity at colder temperatures.

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18
Q

Is Anti-I clinically significant?

A

No, Anti-I is clinically insignificant, although it can vary in reactivity with different adult red cells.

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19
Q

What causes variability in reactivity of Anti-I with adult red cells?

A

The variability is due to different chain structures in the oligosaccharide chains (I antigens are branched while i antigens are linear).

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20
Q

What makes Anti-I a compound antibody?

A

Anti-I also reacts with H, forming a compound antibody.

21
Q

What is Anti-IH, and with which cells does it exhibit stronger agglutination?

A

Anti-IH exhibits stronger agglutination with red cells that have a higher number of H antigens, such as O and A2 cells.

22
Q

Why can Anti-I and Anti-IH cause confusion in serological testing despite being clinically insignificant?

A

Both can interfere with testing due to their reactions, even though they are not clinically significant.

23
Q

How common are allo Anti-I and auto Anti-i antibodies?

A

Allo Anti-I is rare, and Auto Anti-i is uncommon.

24
Q

What conditions are associated with stronger Auto Anti-I?

A

Auto Anti-I is associated with Mycoplasma pneumoniae infections and cold hemagglutinin disease.

25
Q

What conditions are associated with Anti-i?

A

Anti-i is associated with infectious mononucleosis, lymphoproliferative disease, and occasionally cold hemagglutinin disease.

26
Q

What are some frequently encountered cold allo-antibodies?

A

Anti-P1, Anti-M, Anti-N, Anti-Lea, and Anti-Leb.

27
Q

What method would you use to eliminate the M and N antibodies from reacting on a panel?

A

Use enzyme treatment, as it destroys M and N antigens, thereby preventing their reaction on the panel.

28
Q

What method would you use to eliminate the P1, Lea, and Leb antibodies from reacting on a panel?

A

Prewarm technique or cold adsorption can be used to eliminate these antibodies from reacting on a panel.

29
Q

What are some frequently encountered cold auto-antibodies?

A

Anti-IH and Anti-I.

30
Q

What causes differences in antigen levels on RBCs among the subgroups of blood type A?

A

Different A genes code for varying amounts of enzyme, resulting in fewer antigens on the RBC membrane.

31
Q

What antigens are present in the A1 subgroup?

A

The A1 subgroup has both A1 and A antigens, with Anti-B in the plasma.

32
Q

What antigens are present in the A2 subgroup?

A

The A2 subgroup has only the A antigen, with Anti-A1 and Anti-B in the plasma.

33
Q

Why might the A2 subgroup show an extra reaction in reverse cells?

A

The extra reaction occurs because A1 cells are used in reagent racks, which may react with Anti-A1 in A2 subgroup plasma.

34
Q

What percentage of the Group A population belongs to the A1 subgroup?

A

Approximately 80% of the population is in the A1 subgroup.

35
Q

How is the A2 subgroup confirmed?

A

Confirmation is done by phenotyping the patient with Anti-A1 lectin.

36
Q

What is the purpose of testing with Screen Cells I and II in cold antibody screens?

A

To detect other blood group antibodies.

37
Q

What is the purpose of the Auto Control in cold antibody screens?

A

To test for allo or auto antibodies and specifically to test for Anti-IH.

38
Q

Why are Cord Cells used in cold antibody testing?

A

For testing Anti-i or Anti-I, as cord cells have very little or no I antigens on red cells.

39
Q

What is the purpose of using A1 and A2 Cells in cold antibody screens for certain patients?

A

To test for Anti-A1 and Anti-IH, particularly in patients suspected of being in group A or AB.

40
Q

Why are B Cells tested on patients suspected of being group B and AB in cold antibody panels?

A

To test for Anti-IH.

41
Q

What is the reason for using both A1 and B Cells in cold antibody panels for suspected group AB patients?

A

To test for Anti-IH.

42
Q

How can extra reactions due to a subgroup of A be confirmed?

A

By using a cold panel (only A1 cells will be positive) and phenotyping with Anti-A1 lectin. Anti-A1 lectin is derived from the plant Dolichos biflorus.

43
Q

What steps are taken to confirm other blood group antibodies in cold antibody testing?

A

Use a cold panel (Screen Cells I and/or II will be positive), perform a full panel to identify the antibody (using exclusion rules), and ensure the auto control is negative.

44
Q

What are RA/RB cells used for in the context of other blood group antibodies?

A

RA/RB cells are commercially purchased cells used for reverse testing in the ABO group; they are positive when phenotyping, reacting with the antibody in the plasma.

45
Q

How are cold auto antibodies, such as Auto Anti-I or Auto Anti-IH, confirmed?

A

By performing a cold panel (auto control is positive), DAT testing (positive with Anti-C3d), and titration to determine antibody concentration.

46
Q

Which reagent should be used in the AHG test to avoid anti-complement activity?

A

Use Anti-IgG antiglobulin reagent instead of a polyspecific reagent.

47
Q

What readings should be eliminated to avoid reactivity in antibody testing?

A

Eliminate the IS (Immediate Spin) and 37°C readings.

48
Q

What enhancement technique should be avoided, and what should be used instead?

A

Avoid the LISS enhancement technique, use albumin, and increase the incubation period.

49
Q

What technique should be performed to avoid reactivity, and what special steps are involved?

A

Perform the prewarm technique by warming all samples and reagents and using warm saline for washing. Crossmatch units with a prewarm technique to prevent incompatibility.