Identify the blood types of four blood samples from the ABO group by comparison with four samples of which the blood types are known.

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HAEMATOLOGY II

AIM : to identify the blood types of four blood samples from the ABO group by comparison with four samples of which the blood types are known.

INTRODUCTION

Numerous blood groups have been identified, for example ABO, Rhesus, Duffy and Lewis amongst others.  Within a blood group there are different types depending on which antigen is present on the surface of erythrocytes.  Antigen is a shortened name for antibody generator.  An antigen is a glycolipid of which within the ABO system there are two types – A and B.   A cell displaying the A antigen indicates a person of blood type A.  Those with antigen B indicate blood type B.  Some contain both antigens giving type AB and some have neither antigen - this would be blood type O.  

Isoantibodies, also called agglutinins, are contained within the plasma which will react with the antigens if blood types are mixed causing agglutination, clumping of the red cells, and haemolysis (rupture) of red blood cells.  In an individual with blood type A anti-B antibodies are present, in blood type B anti-A antibodies are present and O type contains both A and B antibodies. AB types contain neither antibody.  Antibodies to a particular blood type will not be present in the plasma of an individual of that blood type but there will in all likelihood be antibodies to antigens not present on the red blood cells. The following example illustrates the above : if a sample of blood type B is donated to an individual of blood type A (recipient), the anti-B antibodies in the plasma of the individual with type A will bind with the B antigens associated with the donor’s red blood cells causing rupture or haemolysis of those donated cells.  This would be problematic as those cells donated would be rendered useless. A second, yet milder, reaction is possible between the anti-A antibodies present in the plasma of the donor’s blood and the A antigens of the recipient’s blood.  This would not cause serious problems because of the dilution of the donor’s plasma that would occur.

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For the reasons outlined above it is important that when blood transfusions take place blood types are cross-matched beforehand.  This is done by typing the patient’s blood by mixing a sample of it with various anti-sera to screen for antibodies and checking for agglutination. At room temperature agglutination, and not haemolysis, is visible to the naked eye indicating incompatibility.  It is then cross-matched against the potential donor’s blood  by checking that the plasma of the recipient does not contain any antibodies which would react against the donor erythrocytes.  If none are present the transfusion can go ahead.

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