ABO antigens are inherited through a codominant fashion.
Acidified human anti-B can determine if a patient has acquired B antigen.
Having both A and B alleles presents type AB.
The O gene is an amorph or silent gene (no product).
The locus of the ABO gene is on the long arm of chromosome 9.
H codes for L-fucosyltransferase which adds the immunodominant sugar L-fucose.
Wharton’s jelly is a gelatinous substance on cord blood that requires 4-6x cell washing before forward type and cannot do reverse type still because the jelly is in the plasma.
Fetus begins producing antigens starting at week 5 of fetal life, increasing their production as they grow.
By birth, fetus has about half the antigens they will produce.
A codes for N-acetylgalactosaminyl-transferase which adds the immunodominant sugar N-acetylgalactosamine to the base O-antigen.
ABO antibodies rise shortly after birth as a result of exposure to the outside world.
Rouleaux is an increased protein in the plasma specifically immunoglobulin that can be mistaken for agglutination.
ABO antibodies weaken with age.
Testing patient sample at lower temperatures enhances the reaction.
Under 6 months, children have not developed many antibodies, making the reverse-type unreliable.
Concentration of H antigen on the surface of the RBCs of common blood groups: O> A2> B > A2B > A1> A1B.
Acquired B can result from bacterial infections from GNB, and the deacetylase enzyme can make patients A antigens appear B-like.
B codes for D-galactosyltransferase which adds the immunodominant D-galactose to the base O-antigen.
The most common ABO types in the US are: O, A, B, AB.
Rh + is more common than Rh- each group.
The H gene is dominant to h.
You need at least one H (Homozygous dominant or heterozygous) to produce the transferase that makes H substance.
Without H substance, you cannot add the A and B antigens.
People who do not make H substance have the Bombay phenotype and therefore make antibodies to H and can only be transfused with otherBombay phenotype blood.
Ulex europeus lectin reacts with H antigen. Bombay patients will be negative.
Para-Bombay: Some individuals with the secretor gene can produce H substance in their plasma and other body fluids.
Para-bombay: H substance can float onto their red cells causing weak reactions.
Normal AB patients possess both an A and a B allele.
CISAB arises from a genetic mutation of the ABO gene that allows them to code the transferase enzyme for both A and B.
Subgroups of A include A1 and A2.
A2 can produce anti-A1, causing a discrepancy in the reverse type where the patient will react to a cells.
A2 cells carry less antigen than A1, causing them to react with Ulex europeus anti-h lectin.
Plant lectin from Dolichos biflorus can differentiate A1 from A2, agglutinating A1 cells and not A2.
There are other A subgroups but they are clinically insignificant.
Newer Anti-A reagents are more sensitive to A2 but previously we would use Anti-AB as it picks up on A2 better.