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Questions and Answers
What is the optimal temperature for Anti-U to react?
What is the optimal temperature for Anti-U to react?
Which of the following is NOT a characteristic of Anti-M and Anti-N antibodies?
Which of the following is NOT a characteristic of Anti-M and Anti-N antibodies?
What is the clinical significance of Anti-U?
What is the clinical significance of Anti-U?
Which blood group system does the P1 antigen belong to?
Which blood group system does the P1 antigen belong to?
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Which of these antigens is NOT found on more than 99% of the population?
Which of these antigens is NOT found on more than 99% of the population?
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What is the role of the P antigen in the blood group system?
What is the role of the P antigen in the blood group system?
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How can P1 antigen expression be inhibited?
How can P1 antigen expression be inhibited?
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What is the class of antibody associated with Anti-P1?
What is the class of antibody associated with Anti-P1?
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What is the primary use of the Antiglobulin test?
What is the primary use of the Antiglobulin test?
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Which of the following blood group antibodies is NOT typically associated with clinically significant reactions?
Which of the following blood group antibodies is NOT typically associated with clinically significant reactions?
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How are monoclonal AHG reagents produced?
How are monoclonal AHG reagents produced?
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What type of antibody does the Anti-Lub antibody belong to?
What type of antibody does the Anti-Lub antibody belong to?
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What is the main difference between polyspecific and monospecific AHG reagents?
What is the main difference between polyspecific and monospecific AHG reagents?
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Which of the following is NOT a clinically significant blood group antibody?
Which of the following is NOT a clinically significant blood group antibody?
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Which of the following antibody class is primarily responsible for causing hemolytic disease of the fetus and newborn (HDFN)?
Which of the following antibody class is primarily responsible for causing hemolytic disease of the fetus and newborn (HDFN)?
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Which of the following is a characteristic of monoclonal AHG reagents?
Which of the following is a characteristic of monoclonal AHG reagents?
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How can autoantibodies be removed from a patient's serum?
How can autoantibodies be removed from a patient's serum?
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Which of the following is NOT a factor that influences the sensitivity of an antibody screening test?
Which of the following is NOT a factor that influences the sensitivity of an antibody screening test?
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What is the principle behind the adsorption technique used to remove antibodies from serum?
What is the principle behind the adsorption technique used to remove antibodies from serum?
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Why is using human platelet concentrate particularly useful for adsorbing HLA-related blood group antibodies from serum?
Why is using human platelet concentrate particularly useful for adsorbing HLA-related blood group antibodies from serum?
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A negative result on a 3-cell antibody screen indicates a 95% confidence rate that there are no clinically significant antibodies. What is the main limitation of this 3-cell screen?
A negative result on a 3-cell antibody screen indicates a 95% confidence rate that there are no clinically significant antibodies. What is the main limitation of this 3-cell screen?
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Which of these is an advantage of using a monospecific AHG reagent?
Which of these is an advantage of using a monospecific AHG reagent?
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Which of the following is a disadvantage of using a polyspecific AHG reagent?
Which of the following is a disadvantage of using a polyspecific AHG reagent?
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What is the main purpose of an indirect antiglobulin test (IAT)?
What is the main purpose of an indirect antiglobulin test (IAT)?
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Which of the following is NOT a reason why a direct antiglobulin test (DAT) may be required?
Which of the following is NOT a reason why a direct antiglobulin test (DAT) may be required?
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Which of the following is a potential clinical situation in which an antigen-antibody complex could form in-vivo?
Which of the following is a potential clinical situation in which an antigen-antibody complex could form in-vivo?
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What is the principle behind the direct antiglobulin test (DAT)?
What is the principle behind the direct antiglobulin test (DAT)?
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Why is it important to consider the patient's diagnosis, drug therapy, and recent transfusion history when interpreting a positive DAT?
Why is it important to consider the patient's diagnosis, drug therapy, and recent transfusion history when interpreting a positive DAT?
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What is the rationale for the use of LISS or albumin during the incubation phase of an IAT?
What is the rationale for the use of LISS or albumin during the incubation phase of an IAT?
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Individuals with the Le(a+b-) phenotype have which genotype for the Se gene?
Individuals with the Le(a+b-) phenotype have which genotype for the Se gene?
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Which of the following ABO blood group antigens are present in the secretions of individuals with the Le(a-b+) phenotype?
Which of the following ABO blood group antigens are present in the secretions of individuals with the Le(a-b+) phenotype?
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The Lewis gene is closely linked to which other genes on chromosome 19?
The Lewis gene is closely linked to which other genes on chromosome 19?
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What determines the presence of Leª antigen in secretions?
What determines the presence of Leª antigen in secretions?
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Which of the following accurately describes the phenotype of individuals with the Le(a-b-) phenotype?
Which of the following accurately describes the phenotype of individuals with the Le(a-b-) phenotype?
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Which of the following statements accurately describes individuals with the sese genotype?
Which of the following statements accurately describes individuals with the sese genotype?
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What is the primary difference between Le(a+b-) and Le(a-b+) individuals?
What is the primary difference between Le(a+b-) and Le(a-b+) individuals?
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Which of the following phenotypes is characterized by the presence of both Leª and Leb antigens on RBCs?
Which of the following phenotypes is characterized by the presence of both Leª and Leb antigens on RBCs?
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What characterizes the Lewis Blood Group System distinctively compared to other blood group systems?
What characterizes the Lewis Blood Group System distinctively compared to other blood group systems?
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Which of the following are the three common phenotypes of the Lewis Blood Group System?
Which of the following are the three common phenotypes of the Lewis Blood Group System?
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How are the Lewis antigens Leª (LE1) and Leb (LE2) produced?
How are the Lewis antigens Leª (LE1) and Leb (LE2) produced?
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What role does the Se (secretor) gene play in the Lewis Blood Group System?
What role does the Se (secretor) gene play in the Lewis Blood Group System?
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In which chromosome is the Se gene located?
In which chromosome is the Se gene located?
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What differentiates the enzymes produced by the Se and H genes?
What differentiates the enzymes produced by the Se and H genes?
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How are the Lewis antigens like Leª (LE1) and Leb (LE2) eluted from red blood cells?
How are the Lewis antigens like Leª (LE1) and Leb (LE2) eluted from red blood cells?
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What type of sugars do fucosyltransferases transfer, relevant to the Lewis Blood Group System?
What type of sugars do fucosyltransferases transfer, relevant to the Lewis Blood Group System?
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Study Notes
Lewis Blood Group System
- The Lewis blood group system is unique because its antigens are not synthesized by red blood cells (RBCs). Instead, they are adsorbed onto the RBC membrane from the plasma.
- The two main antigens in the Lewis blood group system are Leª and Leb.
- The three common phenotypes of the Lewis blood group system are Le(a+b-), Le(a-b+), and Le(a-b-).
- Leª and Leb antigens are not antithetical (opposite).
- These antigens are encoded by two fucosyltransferase genes, Le and Se, which are independent genes.
- Fucosyltransferases are enzymes that transfer an L-fucose sugar from a donor substrate to an acceptor substrate.
- Lewis antigens are glycolipids acquired by adsorption from the surrounding plasma onto RBCs.
- They are not manufactured by the red blood cell.
Lewis Phenotypes in Secretions and Se
- The three Lewis phenotypes represent the presence or absence of Lewis and secretor enzymes.
- The secretor (Se) gene is located on chromosome 19.
- The two alleles at the chromosome 19 locus are Se and se.
- The se allele is an amorph, producing no detectable product in secretions.
Enzyme Production by Se and H Genes
- The enzymes produced by the Se and H genes are fucosyltransferases, but their functions differ.
- The H-gene enzyme adds L-fucose to Type 2 precursor chains on RBC membranes.
- The Se-gene enzyme adds L-fucose to Type 1 precursor chains, which are found in bodily fluids.
- Individuals with the secretor genotype (SeSe or Sese) are secretors, while individuals with the non-secretor genotype (sese) are non-secretors.
- Non-secretors lack ABH antigens in their secretions.
Lewis Phenotypes
- Le(a+b-): This phenotype is produced by inheriting the Lewis gene (LE or FUT3) but not the secretor gene (SE or FUT2). Le and H antigens are produced when Le and H genes are present. The genotype is sese. It is a non-secretor of A,B,H antigens.
- Le(a-b+): This phenotype is produced by inheriting both the Lewis gene (LE or FUT3) and the secretor gene (SE or FUT2). Le, H, and Se genes are present. A, B, H and Leb (LE2) antigens are produced.
- Le(a-b-): This phenotype is caused by not inheriting the Lewis gene (lele). Le(a-b-) secretors have the Se gene and produce A, B, H and Leb (LE2) antigens in their secretions. Le(a-b-) non-secretors have no antigens in their secretions.
Development and Changes of Lewis Antigens after Birth
- Lewis antigens are not fully developed at birth, but appear shortly thereafter as they are adsorbed onto the red blood cells.
- The phenotype of cord blood and newborns is Le(a-b-).
- Individuals with Le and sese genotypes do not have detectable Lewis antigens on cord cells, but secrete Leª in their saliva.
MNS Blood Group System
- The genes of the MNS BGS are GYPA and GYPB.
- The phenotypes of the MNS BGS are M+N-, M+N+, M-N+, and M-N-.
- The S and s antigens are distinct from M and N antigens, but are genetically linked.
Anti-M and Anti-N
- Anti-M is a cold antibody (optimally reactive at 4°C), and is rarely clinically significant.
- Anti-N is a cold antibody and is rarely clinically significant.
Other Antigens
- Anti-S, anti-s, and anti-U are uncommon, usually IgG antibodies, and are optimally reactive at 37°C.
- Anti-U is commonly found in the serum of prenatal patients.
- The various antigens, such as Lea, Leb, K, k, and so on are elaborated in their specific sections.
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Description
Test your knowledge on blood group antibodies with this comprehensive quiz. Explore key concepts such as the characteristics of Anti-U, Anti-M, and Anti-N antibodies, as well as the clinical significance of various antigens. Perfect for medical students and professionals in immunohematology.