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LEARNING OUTCOMES
• Give the physiological basis of classification of blood groups.
• List the agglutinogens and agglutinins of various blood groups.
• Describe the pattern of inheritance of the A, B and Rhesus
antigens.
• State ‘Landsteiner’s law’.
• Explain why O, Rhblood group is a universal donor, and AB, Rh+
blood group is a universal recipient. Cross matching and its
importance.
• Describe the pathogenesis of hemolytic disease of the newborn
(erythroblastosis foetalis). Give the physiologic basis of the
strategy used to prevent hemolytic disease of the newborn.
Blood Group Systems
• ABO system
• Rh system
• M,N system
• Kell system
• Lewis system
ABO system
• Depends on the presence or absence of blood
group antigens (agglutinogens ) a and b on the
surface of red cells.
BLOOD ANTIGEN
GROUP
A a antigen
B b antigen
AB both a and b
O none
AGGLUTININS
• Antibodies against agglutinogens called
agglutinins
• Present in plasma
Agglutinin α acts against antigen a
Agglitinin β acts against antigen b
LANDSTEINERS LAW
1. If an agglutinogen/s is present on the red cells
of an individual , the corresponding agglutinin/s
must be absent in the plasma
2. If an agglutinogen/s is absent on the red cells,
the corresponding agglutinin/s must be present
in the plasma
Inheritance of Blood Groups
Gene from Blood group Genotype
each parent
A+A or A AA/AO
A+O
B+B or B+O B BB/BO
A+B AB AB
O+O O OO
Rh SYSTEM OF BLOOD GROUPS
• Red cells of about 90 % humans contain Rh antigen
(Rh positive)
• ERYTHROBLASTISIS FETALIS
• Severe anemia and jaundice
• Hydrops fetalis
• Fetal death in utero or
• The baby dies soon after birth or
• Newborn baby has severe anemia and
jaundice
• Fetal peripheral blood shows erythroblasts
• Kernicterus develops
Bilirubin deposited in basal ganglia leading to
permanent brain damage
• Treatment: Exchange blood transfusion with
ABO compatible Rh– blood
Prevention is more important
• After first delivery inject Rh antibodies ( anti D
injections) to the mother. It destroys Rh + fetal
cells before they get implanted in the
maternal immunological competent tissues