Immuhematology- Testing for Antibodies Flashcards

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1
Q
  1. A patient has the Lewis phenotype Le(a−b−). An
    antibody panel reveals the presence of anti-Lea.
    Another patient with the phenotype Le(a−b+) has
    a positive antibody screen; however, a panel
    reveals no conclusive antibody. Should anti-Lea be
    considered as a possibility for the patient with the
    Le(a−b+) phenotype?
    A. Anti-Lea should be considered as a possible
    antibody
    B. Anti-Lea may be a possible antibody, but further
    studies are needed
    C. Anti-Lea is not a likely antibody because even Leb
    individuals secrete some Lea
    D. Anti-Lea may be found in saliva but not
    detectable in serum
A

C. Anti-Lea is not a likely antibody because even Leb
individuals secrete some Lea

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2
Q
  1. A technologist is having great difficulty resolving
    an antibody mixture. One of the antibodies is antiLea. This antibody is not clinically significant in
    this situation, but it needs to be removed to reveal
    the possible presence of an underlying antibody of
    clinical significance. What can be done?
    A. Perform an enzyme panel
    B. Neutralize the serum with saliva
    C. Neutralize the serum with hydatid cyst fluid
    D. Use DTT (dithiothreitol) to treat the panel cells
A

B. Neutralize the serum with saliva

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3
Q
  1. What type of blood should be given to an
    individual who has an anti-Leb that reacts 1+ at
    the IAT phase?
    A. Blood that is negative for the Leb antigen
    B. Blood that is negative for both the Lea and Leb
    antigens
    C. Blood that is positive for the Leb antigen
    D. Lewis antibodies are not clinically significant, so
    any type of blood may be given
A

A. Blood that is negative for the Leb antigen

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4
Q
  1. Which of the following statements is true
    concerning the MN genotype?
    A. Antigens are destroyed using bleach-treated cells
    B. Dosage effect may be seen for both M and N
    antigens
    C. Both M and N antigens are impossible to detect
    because of cross-interference
    D. MN is a rare phenotype seldom found in routine
    antigen typing
A

B. Dosage effect may be seen for both M and N
antigens

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5
Q
  1. Anti-M is sometimes found with reactivity
    detected at the immediate spin (IS) phase that
    persists in strength to the IAT phase. What is the
    main testing problem with a strong anti-M?
    A. Anti-M may not allow detection of a clinically
    significant antibody
    B. Compatible blood may not be found for the
    patient with a strongly reacting anti-M
    C. The anti-M cannot be removed from the serum
    D. The anti-M may react with the patient’s own
    cells, causing a positive autocontro
A

A. Anti-M may not allow detection of a clinically
significant antibody

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6
Q
  1. A patient is suspected of having paroxysmal
    cold hemoglobinuria (PCH). Which pattern
    of reactivity is characteristic of the Donath–
    Landsteiner antibody, which causes this condition?
    A. The antibody attaches to RBCs at 4°C and causes
    hemolysis at 37°C
    B. The antibody attaches to RBCs at 37°C and
    causes agglutination at the IAT phase
    C. The antibody attaches to RBCs at 22°C and
    causes hemolysis at 37°C
    D. The antibody attaches to RBCs and causes
    agglutination at the IAT phase
A

A. The antibody attaches to RBCs at 4°C and causes
hemolysis at 37°C

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7
Q
  1. How can interfering anti-P1 antibody be removed
    from a mixture of antibodies?
    A. Neutralization with saliva
    B. Agglutination with human milk
    C. Combination with urine
    D. Neutralization with hydatid cyst fluid
A

D. Neutralization with hydatid cyst fluid

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8
Q
  1. Which antibody is frequently seen in patients with
    warm autoimmune hemolytic anemia?
    A. Anti-Jka
    B. Anti-e
    C. Anti-K
    D. Anti-Fyb
A

B. Anti-e

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9
Q
  1. An antibody shows strong reactions in all test
    phases. All screen and panel cells are positive. The
    serum is then tested with a cord cell and the
    reaction is negative. What antibody is suspected?
    A. Anti-I
    B. Anti-i
    C. Anti-H
    D. Anti-p
A

A. Anti-I

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10
Q
  1. Which group of antibodies is commonly found as
    cold agglutinins?
    A. Anti-K, anti-k, anti-Jsb
    B. Anti-D, anti-e, anti-C
    C. Anti-M, anti-N
    D. Anti-Fya, anti-Fyb
A

C. Anti-M, anti-N

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11
Q
  1. Which of the following antibodies
    characteristically gives a refractile mixed-field
    appearance?
    A. Anti-K
    B. Anti-Dia
    C. Anti-Sda
    D. Anti-s
A

C. Anti-Sda

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12
Q
  1. What does the 3+3 rule ascertain?
    A. An antibody is ruled in
    B. An antibody is ruled out
    C. 95% confidence that the correct antibody has
    been identified
    D. 95% confidence that the correct antibody has
    not been identified
A

C. 95% confidence that the correct antibody has
been identified

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13
Q
  1. The k (Cellano) antigen is a high-frequency
    antigen and is found on most red cells. How
    often would one expect to find the corresponding
    antibody?
    A. Often, because it is a high frequency antibody
    B. Rarely, because most individuals have the
    antigen and therefore would not develop the
    antibody
    C. It depends upon the population, because certain
    racial and ethnic groups show a higher frequency
    of anti-k
    D. Impossible to determine without consulting
    regional blood group antigen charts
A

B. Rarely, because most individuals have the
antigen and therefore would not develop the
antibody

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14
Q
  1. Which procedure would help to distinguish
    between an anti-e and anti-Fya in an antibody
    mixture?
    A. Lower the pH of test serum
    B. Run an enzyme panel
    C. Use a thiol reagent
    D. Run a LISS pane
A

B. Run an enzyme panel

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15
Q
  1. Which characteristics are true of all three of
    the following antibodies: anti-Fya, anti-Jka,
    and anti-K?
    A. Detected at the IAT phase; may cause hemolytic
    disease of the newborn and hemolytic transfusion
    reactions
    B. Not detected with enzyme-treated cells
    C. Requires the IAT technique for detection;
    usually not associated with HDN
    D. Enhanced reactivity with enzyme-treated cells;
    may cause severe hemolytic transfusion reactions
A

A. Detected at the IAT phase; may cause hemolytic
disease of the newborn and hemolytic transfusion
reactions

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16
Q
  1. A patient is admitted to the hospital. Medical
    records indicate that the patient has a history of
    anti-Jka. When you performed the type and screen,
    the type was O positive and screen was negative.
    You should:
    A. Crossmatch using units negative for Jka antigen
    B. Crossmatch random units, since the antibody is
    not demonstrating
    C. Request a new sample
    D. Repeat the screen with enzyme-treated screening
    cells
A

A. Crossmatch using units negative for Jka antigen

17
Q
  1. A technologist performs an antibody study and
    finds 1+ and weak positive reactions for several of
    the panel cells. The reactions do not fit a pattern.
    Several selected panels and a patient phenotype do
    not reveal any additional information. The serum
    is diluted and retested, but the same reactions
    persist. What type of antibody may be causing
    these results?
    A. Antibody to a high-frequency antigen
    B. Antibody to a low-frequency antigen
    C. High titer low avidity (HTLA)
    D. Anti-HLA
A

C. High titer low avidity (HTLA)

18
Q
  1. An antibody is detected in a pregnant woman and
    is suspected of being the cause of fetal distress. The
    antibody reacts at the IAT phase but does not react
    with DTT-treated cells. This antibody causes in
    vitro hemolysis. What is the most likely antibody
    specificity?
    A. Anti-Lea
    B. Anti-Lua
    C. Anti-Lub
    D. Anti-Xga
A

C. Anti-Lub

19
Q
  1. What sample is best for detecting complementdependent antibodies?
    A. Plasma stored at 4°C for no longer than
    24 hours
    B. Serum stored at 4°C for no longer than 48 hours
    C. Either serum or plasma stored at 20°C–24°C no
    longer than 6 hours
    D. Serum heated at 56°C for 30 minutes
A

B. Serum stored at 4°C for no longer than 48 hours

20
Q
  1. Which antibody would not be detected by group
    O screening cells?
    A. Anti-N
    B. Anti-A1
    C. Anti-Dia
    D. Anti-k
A

B. Anti-A1

21
Q
  1. Refer to Panel 1. Which antibody is most likely
    implicated?
    A. Anti-Fyb
    B. Anti-Jkb
    C. Anti-e
    D. Anti-c and anti-K
A

B. Anti-Jkb

22
Q
  1. Refer to Panel 2. Which antibody specificity is
    most likely present?
    A. Anti-S and anti-E
    B. Anti-E and anti-K
    C. Anti-Lea and anti-Fyb
    D. Anti-C and anti-K
A

D. Anti-C and anti-K

23
Q
  1. On Panel 2, which of the following antibodies
    could not be ruled out?
    A. Anti-Jkb
    B. Anti-C
    C. Anti-M
    D. Anti-Fyb
A

B. Anti-C

24
Q
  1. On Panel 2, which cells are homozygous for C?
    A. 1, 2, 3
    B. 1, 2, 9
    C. 3, 4, 7
    D. 7, 8, 10
A

B. 1, 2, 9

25
Q
  1. A 77-year-old female is admitted to a community
    hospital after a cardiac arrest. History includes an
    abdominal aortic aneurysm 2 years ago in which
    she received 6 units of packed cells. Her blood type
    is A positive and antibody screen is positive at
    AHG phase in screening cells II and III. A panel
    is performed using LISS. Referring to panel 3,
    which antibodies are likely implicated?
    A. C and K
    B. Jka and c
    C. E and c
    D. Fya and M
A

C. E and c

26
Q
  1. What observation is apparent with one of the
    antibodies present on Panel 3?
    A. One antibody is only reacting with heterozygous
    cells
    B. Both antibodies are only reacting with
    homozygous cells
    C. One antibody is only reacting with homozygous
    cells
    D. Both antibodies are exhibiting dosage
A

C. One antibody is only reacting with homozygous
cells