RH, Lewis, MNS BLOOD GROUP SYSTEMS

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1
Identify the problem category for forward and reverse grouping miscellaneous causes.
Group IV Discrepancies
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2
Identify three general antibody-related causes of Group IV discrepancies.
Cold reactive autoantibodies, Unexpected ABO isoagglutinins, Unexpected non-ABO alloantibodies
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3
Fill in the blank: Tactivation infection by ____________ is a cause associated with cold reactive autoantibodies.
M. pneumoniae
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4
Identify the acronyms associated with inactivation under cold reactive autoantibodies in the notes.
HEMPAN/CDAI
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5
True or False: Mutations are considered inherited forms of Group IV discrepancies.
True
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6
Identify two patient situations that can cause the presence of more than one ABO group of RBCs.
Transfusion, BM or stem cell transplant
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7
Identify the condition where patient RBCs are agglutinated by most adult human sera but not by autologous serum or newborn sera.
Polyagglutination
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8
Identify the patient's probable blood group if forward grouping shows Anti-A 2+ and Anti-B 4+, while reverse grouping shows A cells 4+ and B cells 2+.
B
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9
True or False: Cold agglutinins never react above 30°C.
True
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10
Identify the initial resolution step for patient RBCs in forward typing when cold autoantibodies cause a discrepancy.
Wash with saline at 37°C 3 times, and retype
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11
Fill in the blank: If washing at 37°C fails to resolve cold autoantibodies in forward typing, treat the patient's RBCs with ____________ dithiothreitol.
0.01M DTT
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12
Identify the full chemical name for the abbreviation DTT.
Dithiothreitol
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13
Identify the temperature to which reagent RBCs and serum must be warmed, mixed, tested, and read during reverse typing resolution for cold autoantibodies.
37°C
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14
Identify the procedure performed to remove cold autoantibodies if reverse typing remains unresolved after warming to 37°C.
Cold autoadsorption
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15
Identify the patient's probable blood group if forward grouping shows Anti-A 4+ and Anti-B 4+, while reverse grouping shows A cells 1+ and B cells 0.
AB
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16
Identify the specific circulating antibody in the serum causing the 1+ reaction with A cells in the unexpected ABO isoagglutinins example.
Anti-A1
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17
Fill in the blank: To resolve unexpected ABO isoagglutinins, determine the specificity of the antibody by testing cells with anti-A1 ____________ and serum with A1, A2, and O cells.
Lectin
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18
Identify the patient's probable blood group if forward grouping shows Anti-A 4+ and Anti-B 4+, while reverse grouping shows A cells 1+ and B cells 1+.
AB
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19
Identify the resolution steps for unexpected non-ABO alloantibodies where both A and B cells show 1+ reactivity.
Run antibody screen and panel identification
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20
Identify the rare Group IV discrepancy where the anti-B antigen will be agglutinated due to a reagent component antibody.
Antibody to acriflavine
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21
Identify the rare phenotype where an offspring inherits both A and B genes from one parent on the same side.
Cis-AB phenotype
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22
Fill in the blank: In genetics, genes located on the same side are termed ____________, while those on opposite sides are termed trans.
Cis
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23
Identify the scientists who proposed the two-gene model (RHD and RHCE) for the Rh blood group system.
Tippett
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24
Identify the chromosome where the RHD and RHCE genes are located.
Chromosome 1
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25
Identify the specific Rh antigen whose expression is controlled by the RHD gene.
RhD
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26
Identify the four Rh polypeptide combinations controlled by the RHCE gene.
RhCe, RhcE, RhCE, Rhce
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27
True or False: Codominance is observed in the expression of RHCE gene products.
True
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28
Identify the chromosome where the RHAG gene is located.
Chromosome 6
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29
Fill in the blank: The RHAG gene codes for a ____________ that must be present to express Rh antigen, though by itself it cannot express any Rh antigen.
Co-expressor
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30
True or False: Mutations in the RHAG gene can cause significantly altered RhD and RhCE proteins.
True
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31
Identify the Rh nomenclature system that involves three separate closely linked genes (D, C, E) inherited as a group.
Fisher-Race
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32
Identify the corresponding RBC surface antigens expressed by the Fisher-Race genes D, C/c, and E/e.
D antigen, C/c antigen, E/e antigen
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33
Fill in the blank: In the Fisher-Race system, the absence of the D antigen is designated as ____________.
d
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34
True or False: The 'd' antigen is a placeholder notation and not an actual physical antigen.
True
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35
Identify the Rh nomenclature system based on the theory that a single locus on a gene carries the entire Rh system.
Wiener
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36
Fill in the blank: According to Wiener's terminology, each Rh gene produces an ____________ containing a series of three blood factors.
Agglutinogen
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37
True or False: In Wiener nomenclature, each blood factor is an antigen recognized by an antibody.
True
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38
Identify what the agglutinogen represents in terms of haplotypes in the Wiener system.
A single haplotype composed of 3 different antigens
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39
Convert the Fisher-Race haplotype DCe into Wiener shorthand terminology.
R1
40
Convert the Fisher-Race haplotype DcE into Wiener shorthand terminology.
R2
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41
Convert the Fisher-Race haplotype Dce into Wiener shorthand terminology.
R0
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42
Convert the Fisher-Race haplotype DCE into Wiener shorthand terminology.
Rz
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43
Convert the Fisher-Race haplotype dce into Wiener shorthand terminology.
r
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44
Convert the Fisher-Race haplotype dCe into Wiener shorthand terminology.
r'
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45
Convert the Fisher-Race haplotype dcE into Wiener shorthand terminology.
r''
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46
Convert the Fisher-Race haplotype dCE into Wiener shorthand terminology.
ry
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47
Fill in the blank: In Wiener terminology, a single prime (') or the number 1 corresponds to the presence of the ____________ antigen.
C
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48
Fill in the blank: In Wiener terminology, a double prime (") or the number 2 corresponds to the presence of the ____________ antigen.
E
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49
Fill in the blank: In Wiener terminology, the letter 'o' or number 0 corresponds to the presence of ____________ antigens.
ce
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50
Fill in the blank: In Wiener terminology, the letter 'z' or 'y' corresponds to the presence of ____________ antigens.
CE
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51
Identify how genotype and phenotype are designated in Wiener shorthand notation using superscripts and subscripts.
Genotype uses superscripts, Phenotype uses subscripts
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52
Identify the Wiener blood factor designation for the D antigen.
Rh0
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53
True or False: In Wiener terminology, capital letters C and E are designated using 'rh' where the 'r' precedes the 'h'.
True
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54
True or False: In Wiener terminology, lowercase letters c and e are designated using 'hr' where the 'h' precedes the 'r'.
True
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55
Identify the prime notation used for C/c antigens in Wiener terminology.
Single prime
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56
Identify the prime notation used for E/e antigens in Wiener terminology.
Double prime
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57
Identify the Wiener designation for the 'd' antigen.
No designation
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58
Identify the most common Rh genotype/haplotype in Black populations.
R0r
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59
Identify the most common Rh genotype/haplotype in Asians and Whites.
R1r
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60
List the Rh haplotypes in decreasing order of frequency among African-Americans.
R0 > r > R1 > R2
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61
List the Rh haplotypes in decreasing order of frequency among Caucasians.
R1 > r > R2 > R0
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62
Identify the Fisher-Race genotype corresponding to the Wiener notation r'r'.
dCe/dCe
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63
Identify the Fisher-Race genotype corresponding to the Wiener notation r''r.
dcE/dce
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64
Identify the Fisher-Race genotype corresponding to the Wiener notation r''r''.
dcE/dcE
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65
Identify the Fisher-Race genotype corresponding to the Wiener notation r'r'' or ryr.
dCe/dcE or dCE/dce
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66
Identify the Rh nomenclature system that uses alpha-numeric terminology and has no genetic basis.
Rosenfield
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67
In Rosenfield nomenclature, identify what a minus sign (-) preceding a number designates.
Absence of the antigen
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68
Identify the Rosenfield numbers assigned to the five principal Rh antigens: D, C, E, c, and e.
Rh1, Rh2, Rh3, Rh4, Rh5
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69
Convert the Fisher-Race phenotype D+, C+, E+, c+, e+ into Rosenfield notation.
Rh:1,2,3,4,5
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70
Fill in the blank: In Rosenfield notation, if an antigen has not been typed, its number will ____________ in the sequence.
Not appear
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71
Identify the nomenclature system that adopts a 6-digit number for each authenticated antigen.
International Society of Blood Transfusion
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72
Identify the acronym for the International Society of Blood Transfusion.
ISBT
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73
In ISBT nomenclature, identify what the first three numbers and the last three numbers represent.
First 3 represent the system, last 3 represent antigenic specificity
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74
Identify the 3-digit system number assigned to the Rh Blood Group by the ISBT.
004
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75
Identify the full 6-digit ISBT number for the D antigen.
004001
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76
Identify the full 6-digit ISBT number for the C antigen.
004002
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77
Identify the full 6-digit ISBT number for the E antigen.
004003
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78
Identify the full 6-digit ISBT number for the c antigen.
004004
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79
Identify the full 6-digit ISBT number for the e antigen.
004005
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80
Identify the "Big 4" most common Rh genotypes using Wiener shorthand.
R1, R2, r, R0
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81
True or False: Rh antigens are non-glycosylated polypeptides that contain no carbohydrates.
True
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82
True or False: Rh antigens are soluble and widely expressed on body tissues.
False
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83
True or False: Rh antigens are well developed at birth and can easily cause Hemolytic Disease of the Newborn.
True
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84
Identify the most immunogenic RBC antigen after the A and B antigens.
D antigen
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85
List the five principal Rh antigens in decreasing order of their immunogenicity.
D > c > E > C > e
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86
Identify the ethnic group in which the Weak D phenotype is most common.
Blacks
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87
Identify three methods used to detect or confirm Weak D expression.
Enzyme treatment, more sensitive anti-D IAT, Adsorption elution studies
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88
Identify the type of Weak D cause that is due to a positional effect where the C allele is in trans position to the RHD allele.
C in Trans to RHD
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89
True or False: Individuals with positional Weak D (C in trans) have normal Rh antigens and can receive D+ RBCs safely.
True
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90
Identify the cause of Weak D where the inherited RHD gene codes for a lower number of fully expressed D antigens.
Genetic weak D
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91
True or False: Genetic weak D individuals frequently produce anti-D alloantibodies because the alterations are inside the RBC.
False
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92
Identify the term used when one or more epitopes within the D protein are missing or altered.
Partial D
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93
True or False: Partial D individuals can form alloantibodies against missing epitopes, which can cause HDN.
True
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94
Identify how a Partial D individual is classified when acting as a blood donor versus when acting as a recipient.
Rh positive as a donor, Rh negative as a recipient
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95
Identify the rare Rh phenotype characterized by the complete absence of C, c, E, and e antigens, but an increased number of D antigens.
Rh Deletion
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96
Identify the rare Rh phenotype where there is absolutely no Rh antigen expression on the RBCs.
Rh Null
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97
List the clinical and hematologic characteristics associated with the Rh Null syndrome.
Hemolytic anemia, reticulocytosis, stomatocytosis, decreased Hb, Hct, and haptoglobin, increased bilirubin and HbF
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98
Identify the type of Rh Null caused by a mutation in the RHAG gene despite having normal RHD and RHCE genes.
Regulator Type
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99
Identify the type of Rh Null caused by a deleted RHD gene or mutation in the RHCE gene while having a normal RHAG gene.
Amorphic Type
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100
Identify the condition characterized by partial suppression of the Rh gene resulting in weakened Rh antigen expression due to an RHAG mutation.
Rh mod
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101
Identify the compound antigen expressed only when 'c' and 'e' are in the cis position on the same chromosome.
f
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102
Identify the antigen caused by a single amino acid change on the RhCe protein.
Cw
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103
Identify the compound antigen expressed when both 'C' and 'e' are present.
RhX
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104
Identify the antigen that is present on most D+ and C+ RBCs but absent on D-C- cells.
G
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105
Identify the descriptive term used for exceptionally strong D antigen expression due to the total absence of Cc/Ee expression.
Exalted
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106
True or False: Rh antibodies are immune antibodies that are not naturally occurring and require prior sensitization through pregnancy or transfusion.
True
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107
Identify the immunoglobulin class of Rh antibodies and their optimal reaction temperature.
IgG, 37°C
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108
True or False: Rh antibodies can cross the placenta and cause Hemolytic Disease of the Newborn.
True
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109
Identify the primary site of destruction (hemolysis) for hemolytic transfusion reactions caused by Rh incompatibilities.
The liver
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110
Identify the minimum volume of Rh+ RBCs capable of stimulating antibody production in an Rh negative individual.
0.1 mL
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111
Identify the specific antibody activity that warm autoantibodies often appear to mimic.
Anti-e like specificity
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112
Identify the chromosome where the LW blood group system gene (ICAM4) is located.
Chromosome 19p
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113
Identify the membrane protein on which LW antigens reside.
ICAM-4
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114
Identify the chemical treatment used to differentiate between the D antigen and the LW antigen by destroying LW while leaving D intact.
DTT
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115
True or False: The D antigen is resistant to and not denatured by dithiothreitol treatment.
True
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116
Identify the animals used to produce antibodies when exposed to Rhesus monkey RBCs in early LW system discovery.
Rabbits or guinea pigs
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117
Identify the required temperature range inside the Rh viewbox for the slide method of Rh typing.
45-50°C
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118
Fill in the blank: Agglutination in the slide method of Rh typing must be read within ____________ minutes to avoid false positive results from drying.
2
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119
Identify the optimal concentration of the red cell suspension prepared for the tube method of Rh typing.
2-5%
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120
Identify the reagent added to link non-agglutinating antibodies during the late phases of the tube method or Weak D testing.
AHG reagent
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121
List the three quality control purposes of adding Check Cells/Control cells to a negative AHG test.
Confirm AHG was added, Verify AHG potency, Ensure proper washing to remove unbound antibodies
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122
Fill in the blank: If check cells do not show agglutination (negative result), the entire test must be ____________.
Repeated
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123
True or False: Unbound antibodies left in the tube due to improper washing will neutralize the AHG reagent.
True
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124
Identify three common reagents used in routine Rh typing procedures.
Bovine Serum Albumin, Anti-D antisera, Rh Control
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125
True or False: Reverse typing is routinely performed for the Rh blood group system.
False
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126
Identify the specific serological test format used to perform Weak D typing.
Indirect Antiglobulin Test
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127
Identify the full name of the acronym IAT.
Indirect Antiglobulin Test
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128
Identify the reagent added after washing the patient's RBCs in the Weak D typing procedure.
AHG or Coombs Reagent
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129
Identify the composition of Check Cells commonly used in blood banking.
Group O Rh positive RBCs coated with Anti-D antibodies
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130
Identify the number of times the tube must be washed with isotonic saline during Weak D typing.
3 times
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131
Identify the donor and recipient Rh classifications for an individual confirmed to be Weak D positive.
Rh positive as a donor, Rh negative as a recipient
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132
Identify the compatible red blood cell types for an AB negative patient in order of preference.
AB negative, A negative, B negative, O negative
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133
True or False: For plasma/FFP transfusions, an O positive patient can safely receive plasma from any ABO blood group.
True
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134
True or False: Any ABO blood type component may be used for platelet and cryoprecipitate transfusions if the patient's identical type is unavailable.
True
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135
Fill in the blank: Rh compatibility considerations strictly apply only to the transfusion of red blood cells and ____________.
Platelets
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136
True or False: An Rh positive patient can safely receive either Rh positive or Rh negative red blood cell components.
True
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137
Identify the ISBT system number for the Lewis blood group system.
007
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138
Identify the gene and chromosome location for the Lewis blood group system.
FUT3, Chromosome 19p
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139
Identify the two primary antigens of the Lewis system.
Lea, Leb
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140
Fill in the blank: Lewis antigens are synthesized in tissues as ____________ and found in secretions before being adsorbed onto the RBC membrane as glycolipids.
Glycoproteins
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141
Identify the immunoglobulin class and thermal property of Lewis antibodies.
IgM, cold reacting
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142
Identify the characteristic Lewis phenotype of newborns at birth.
Le(a-b-)
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143
Identify the specific Lewis antigen that serves as a receptor for Helicobacter pylori.
Leb
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144
Identify the ISBT system number for the MNS blood group system.
002
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145
Identify the three genes and the chromosome location associated with the MNS system.
GYPA, GYPB, GYPE, Chromosome 4q
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146
Identify the specific glycophorin structures that carry the M, N antigens and the S, s, U antigens respectively.
Glycophorin A, Glycophorin B
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147
Identify the MNS system antibodies that are typically cold-reacting IgM or IgG molecules.
Anti-M, Anti-N
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148
Identify the MNS system antibodies that are warm-reacting IgG molecules capable of crossing the placenta and causing HDFN or HTRs.
Anti-S, Anti-s, Anti-U
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149
Identify the specific MNS antibody most commonly found in Black individuals who lack both S and s antigens.
Anti-U
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150
Identify the microbial pathogens that use Glycophorin A and Glycophorin B as receptors on the RBC membrane.
E. coli, Plasmodium falciparum
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151
Fill in the blank: The phenomenon where an antibody reacts more strongly with homozygous cells than heterozygous cells, observed in the MNS system, is called the ____________.
Dosage effect
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152
Identify the ISBT system number and chromosome location for the P1PK blood group system.
003, Chromosome 22q
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153
Identify the primary antigens belonging to the P1PK system.
P1, Pk
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154
Identify the antigen that serves as a receptor for Shiga toxin leading to Hemolytic Uremic Syndrome (HUS).
Pk antigen
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155
Identify the ISBT system number and gene location for the Globoside blood group system.
028, B3GALNT1
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156
Identify the primary antigen of the Globoside system.
P antigen
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157
Identify the virus that utilizes the P globoside antigen as its receptor for entry.
Parvovirus B19
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158
Identify the clinical condition and the autoantibody involved that is associated with the Globoside system.
Paroxysmal Cold Hemoglobinuria, autoanti-P
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