OTHER Blood Group Systems

Cards (24)

  • ISBT OO4 Rh BLOOD GROUP SYSTEM
    • In 1939, Levine and Stetson described a hemolytic transfusion reaction in an obstetrical patient and this was the first noted RH HTR case
    • The most important blood group system associated with HDN
    • The second leading cause of HDN
    • The type of hemolysis is DELAYED AND EXTRAVASCULAR
    • RH genes are inherited as codominant alleles. The product of RH genes are nonglycosylated proteins.
  • TERMINOLOGIES OF Rh System
    1. Fisher-Race (DCE)
    Fisher race antigens: D, C, E, c, e
    “d” = amorph and represents absence of D antigen, reported as Rh (-)
    Rh null phenotype= absence of all RH antigens
    RH null phenotype can be written as Rhnull, —/—, or RH: –1, –2, –3, –4, –5
    Order of Immunogenicity: D>c>E>C>e
  • Wiener believed there was one gene responsible for defining Rh that produced an agglutinogen containing a series of blood factors
  • Rh-Hr terminology
    Wiener believed there was one gene responsible for defining Rh that produced an agglutinogen containing a series of blood factors
  • Rosenfield (Alpha numeric) assigns a number to each antigen of the Rh system in order of its discovery
  • Rosenfield (Alpha numeric)
    The nomenclature has no genetic basis
  • Rosenfield (Alpha numeric) antigens
    • D= Rh1
    • C= Rh2
    • E= Rh3
    • c= Rh4
    • e= Rh5
  • International Society of Blood Transfusion (ISBT) adopted a six-digit number for each blood group specificity
  • International Society of Blood Transfusion (ISBT) numeric terminology
    The first three numbers represent the system and the remaining three represent the antigenic specificity
  • International Society of Blood Transfusion (ISBT) establishes a uniform nomenclature that is both eye and machine readable
  • R0 or Dce - most commonly seen in Black people
    R1 or DCe - commonly seen in WAN (White or Caucasian, Asia, Native Americans)
  • Genetic weak D - D antigens expressed appear to be complete, but few in number
  • Del
    • extremely low number of D antigen that most reagent anti-D are unable to detect.
    • This phenotype occurs most often in individuals of Southeast Asian descent, occurring in up to 30% of that population. It is rare in Caucasians
  • C Trans to D (Position effect)
    - The first mechanism that may result in weakened expression of D antigen was originally described as a position effect or gene interaction effect
    • Allele carrying D is trans (opposite haplotype) to the allele carrying C
  • D mosaic or Partial D
    • Individual with Partial D may produce ANTI-D TO THE MISSING PART
    • One or more parts of the D antigen is missing or altered. The expression can be weakened is when one or more D epitopes within the entire D protein is either missing or altered
  • TEST FOR WEAK D / Du
    Test: Indirect AHG/Coomb’s IAT
    Note: In case of Weak D (+), individually it must be reported as Rh (+)
    In case of blood transfusion/donation;
    Patient: Typed as Rh (-)
    Donor: Typed as Rh (+)
  • Rh ANTIBODIES
    • Most are IgG and reacts optimally at 37’C
    • They are immune antibodies
    • Do not bind complement
    • Causes extravascular hemolysis
    • Causes delayed, extravascular HTR
    • Rh antibodies are usually produced following exposure of the individual’s immune system to foreign RBCs, through either transfusion or pregnancy
    • HDFN caused by Rh antibodies is often severe because the Rh antigens are well developed on fetal cells, and Rh antibodies are primarily IgG, which readily cross the placenta
  • Anti-LW
    • Originally identified as anti-Rh in early experiment involving rabbits immunized with rhesus monkey blood
    • Anti –LW agglutinates Rh+ and Rh- cells except Rh null (--/--)
  • RH null syndrome
    • Individuals lack all RH antigens on their RBCs
    • stomatocytosis,
  • G is an antigen present on most D-positive and all C-positive RBC
  • Saline reactive reagents
    • Saline reactive reagents, which contain IgM immunoglobulin, were the first typing reagents available to test for the D antigen
    • Because saline anti-D is an IgM immunoglobulin, it cannot be used for weak D typing.
  • High protein Anti-D reagents
    • High-protein anti-D reagents (poly-specific reagent) were developed that consisted primarily of IgG anti-D
  • Chemically modified
    • When samples test AB Rh-positive or when the Rh test is performed by itself, a separate saline control or 6% to 8% albumin control must be used to ensure the observed reactions are true agglutination and not a result of spontaneous agglutination.
  • Rh monoclonal antibodies reagents
    • most common Rh antisera
    • It is prepared by hybridoma technology