CorpusHuman Anatomy

Blood groups (ABO and Rh)

Systemata sanguinis

Also known as: ABO blood group, Rhesus, Rh factor, RhD, blood typing

Blood groups are inherited antigens on the surface of red blood cells. The most important are the ABO carbohydrate antigens and the Rh(D) protein. They determine which blood can be safely transfused and the risk of haemolytic disease of the fetus and newborn.

Overview

Universal red-cell donorGroup O (RhD-negative for emergencies)
Universal recipientGroup AB RhD-positive
Universal plasma donorGroup AB
RhD-positive (European ancestry)≈85%

ABO antigens. All ABO antigens are built on a carbohydrate called the H antigen. The A allele codes for an enzyme that adds N-acetylgalactosamine to it. The B allele codes for an enzyme that adds galactose. The O allele codes for no working enzyme, so group O cells carry only the H antigen. A and B are codominant, and O is recessive.

ABO antibodies. In the first months of life, people make IgM antibodies against whichever A or B antigens they lack, probably triggered by similar molecules on gut bacteria. Because these antibodies are already present, an ABO-mismatched transfusion causes immediate destruction of red cells inside the blood vessels. Group O red cells can be given to anyone (universal red-cell donor). Group AB people can receive red cells of any group (universal recipient). For plasma the rules are reversed: AB plasma, which contains no antibodies, can be given to anyone.

Rh system. The Rh system contains more than 50 antigens, but D is the most likely to provoke an immune response. About 85% of people of European descent are Rh(D)-positive, and the proportion is higher in African and East Asian populations. Anti-D is not present naturally. It forms only after a D-negative person is exposed to D-positive cells, through transfusion or pregnancy. Anti-D is IgG, so it can cross the placenta.

Other systems. Other clinically important blood group systems include Kell, Duffy (its antigen is the receptor that Plasmodium vivax uses to enter red cells), Kidd and MNS. People with the rare Bombay (hh) phenotype lack the H antigen altogether.

Function

  • Determine compatibility for blood transfusion and organ transplantation.
  • Determine the risk of alloimmunisation in pregnancy.

Clinical significance

Acute haemolytic transfusion reaction

An ABO-incompatible transfusion, usually caused by a labelling or identification error, causes fever, loin pain, low blood pressure, red or dark urine (haemoglobinuria), DIC and kidney injury within minutes. The transfusion must be stopped immediately. Strict bedside identity checks prevent it.

Haemolytic disease of the fetus and newborn

If an Rh(D)-negative mother carries a D-positive baby, she can make anti-D after fetal cells enter her blood, for example at delivery. In a later D-positive pregnancy, her anti-D crosses the placenta and destroys the baby's red cells. The baby may develop anaemia, jaundice and, in severe cases, hydrops fetalis.

Prevention is to give anti-D immunoglobulin to D-negative mothers routinely during pregnancy (around 28 weeks) and within 72 hours of any sensitising event or of delivering a D-positive baby. The Kleihauer test measures how much fetal blood has entered the mother's circulation, to guide the dose.

ABO incompatibility between mother and baby, usually a group O mother with an A or B baby, causes milder disease and can affect a first pregnancy.

Compiled from standard anatomy and physiology references — see the Cardiovascular System sources. For education only; not medical advice.