Blood Transfusion and Leukocyte Depletion
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Questions and Answers

What is the required enzyme for the normal structure of the T receptor in the Tk polyagglutination?

  • α-1,3-fucosyltransferase
  • β-1,4-galactosyltransferase
  • α-2,3-sialyltransferase
  • β-3-D-galactosyltransferase (correct)
  • Which of the following is NOT a requirement for autologous donation in predeposit autologous donation (AD)?

  • ABO blood group compatibility
  • No strict weight requirement
  • Cross-matching (correct)
  • No age limit
  • What is the function of acetic anhydride in relation to the Tn polyagglutination?

  • Adds a N-acetyl group to galactosamine (correct)
  • Inhibits the α-1,3-fucosyltransferase enzyme
  • Removes a sialic acid group from the oligosaccharide
  • Activates the β-3-D-galactosyltransferase enzyme
  • Which of the following plants is positive for the Tk antigen?

    <p>Glycine soja</p> Signup and view all the answers

    What is the characteristic of the Cad antigen?

    <p>Expressed on the surface of red blood cells</p> Signup and view all the answers

    Which of the following is an example of acquired non-microbially associated polyagglutination?

    <p>VA polyagglutination</p> Signup and view all the answers

    What is the name of the receptor related to the Tn polyagglutination?

    <p>Tetrasaccharide of Thomas and Winzler</p> Signup and view all the answers

    Which of the following is related to the HEMPAS/CDA II?

    <p>Adult i Ag = òH Ag, òSialic acid</p> Signup and view all the answers

    What is the function of the microbial fucosidase in relation to the VA polyagglutination?

    <p>Removes a fucose group from the oligosaccharide</p> Signup and view all the answers

    Which of the following is an example of inherited polyagglutination?

    <p>Tn polyagglutination</p> Signup and view all the answers

    Study Notes

    Leukocyte Depletion Filter

    • Speed of infusion: 15gtts = 1mL, 60gtts = 1min, 1min = 4mL, 1hr = 240mL, Rate = 240mL/hr
    • 1 unit must be completed within 4hrs of blood transfusion

    Polyagglutination

    • Also known as Hubener-Thomsen-Fridenrich Phenomenon
    • Cryptantigens (Hidden Ag9s) are covered with N-acetylneuraminic acid (NANA) or sialic acid
    • When NANA is destroyed (by neuraminidase), Ag9s are exposed
    • Exposed Ag9s react with tetrasaccharide of Thomas & Winzler (T receptor)

    Microbially-Associated Polyagglutination

    • Caused by bacteria that produce neuraminidase:
    • C.perfringens
    • V.cholerae
    • S.pneumoniae
    • E.coli
    • Proteus sp.

    ABO Hemolytic Disease of the Newborn (ABO HDN)

    • Mother: Group O
    • Child: Group A or B

    Group I Discrepancies

    • Weak reacting/missing Ab9s
    • Occurs in:
    • Newborns
    • Elderly patients
    • Hypogammaglobulinemia/agammaglobulinemia

    Group II Discrepancies

    • Weak reacting/missing Ag9s (less frequent)
    • Occurs in:
    • Leukemia
    • Acquired B phenomenon
    • Subgroups of A
    • Hodgkin's disease
    • BGSS (Remedy: Wash RBCs)

    Group III Discrepancies

    • Plasma abnormalities resulting in Rouleaux formation (Plasma factor)
    • Caused by:
    • ñ globulins: MM, WM, HL
    • ñ fibrinogen
    • Dextran and PVP
    • Wharton's jelly (Remedy: Wash cord cells 6-8x)

    Group IV Discrepancies

    • Miscellaneous:
    • Polyagglutination
    • Anti-I (cold agglutinin)
    • Cis > E > C > e (Least immunogenic)

    Rh Blood Group System

    • R or r
    • D or d
    • 1 or 8
    • Ce
    • 2 or 89
    • cE
    • Z or y
    • CE
    • G: D+C+ red cell
    • Rh: 13, 14, 15, 16 (4 different parts of the D mosaic)

    Weak D

    • Genetic weak D: D Ag9s expressed appear complete but few in number
    • D Mosaic (Partial D): if one or more parts of D Ag is missing → weakened expression of D Ag
    • May produce anti-D (Ab against missing fragment)

    Other

    • C Trans: D ---(trans)---> C (Ex. Produce weaker neuraminidase)
    • Tx: Bacterial and viral, unknown mechanism
    • Tk: N-acetyl + galactosamine, Galactosamine = Group B
    • Remedy: Add acetic anhydride
    • VA: Vienna, Virginia, Microbial fucosidase = òfucose = òH
    • Acquired Non-Microbially Associated Polyagglutination:
    • Tn: (-) β-3-D-galactosyltransferase enzyme needed for the normal structure of T receptor (Tetrasaccharide of Thomas and Winzler)
    • Inherited Polyagglutination:
      • Cad: ñSd a
      • HEPAS/CDA II: ñAdult i Ag = òH Ag, òSialic acid
      • Others: HbM – Hyde Park, NOR = Norfolk, Virginia

    Autologous Donation

    • Predeposit AD: Before anticipated transfusion
    • Requirements:
    • No age limit
    • No strict weight requirement (òvol)

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    Description

    This quiz covers the concepts of leukocyte depletion filters, speed of infusion, and polyagglutination phenomenon in blood transfusion. It also touches on cryptantigens and their hiding mechanisms.

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