A1 and A2 Subgroups

These are the most important subgroups in the system.

Frequency: A1 = 80% and A2 = 20%

This means that all other subgroups must be rare.

Differences between A1 and A2: These subgroups have a quantitative difference and perhaps a qualitative difference. The quantitative difference: A1 red cells have about one million A antigens per cell and A2 red cells have about one-quarter million A antigens per cell. This is because the N-acetyl- D-galactosaminyl transferase made by the A1 gene is more efficient at converting H antigen into A antigen than is the transferase made by the A2 gene. The qualitative difference is controversial: some workers think that the A1 and A2 antigens may be slightly chemically different as shown by the fact that some A2 people can produce anti-A1. Others believe the difference to be strictly quantitative, i.e., the anti-A1 made by A2 persons is really an autoantibody that will not react visibly with the patient's own cells because of too few A antigenic sites.

Development at birth: The A1 antigen is very poorly developed at birth and newborns usually type as A2.

Significance: Usually we do not care whether a group A person is A1 or A2. In routine tests both react well with anti-A. Sometimes, however, a group A2 or A2B person will produce an anti-A1 which results in an ABO discrepancy that must be resolved (Table 4-3).

Table 4-3. ABO discrepancies due to anti-A1.

Group anti-A anti-B A1 cells B cells
A2 4+ -- 2+ 4+
A2B 4+ 4+ 1+ --

About 1-8% of group A2 people and 22-35% of A2B people will make anti-A1. When this happens we must resolve the discrepancy in order to determine the person's true ABO group. (For simplicity, consider about 2% of A2 and 25% of A2B people to make anti-A1.)

NOTE: Usually anti-A1 produced by A2 people is a harmless IgM cold agglutinin that reacts best at 4°C, may react at RT (in the ABO group), but will not react at 37°C. Rarely, anti-A1 can be clinically significant and react at 37°C.

Resolution of discrepancies caused by anti-A1


A1 and A2 Subgroups

©1999 Division of Medical Laboratory Science
University of Alberta