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Blood Grouping 27MARCH2016

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0% found this document useful (0 votes)
26 views6 pages

Blood Grouping 27MARCH2016

Uploaded by

prasanna aiyer
Copyright
© © All Rights Reserved
We take content rights seriously. If you suspect this is your content, claim it here.
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1

Blood grouping
Introduction :

 In 1900, Karl Landsteiner first reported A and B antigens on the surface of human red
blood cells
 He divided human red cells into three groups A, B and O
 In 1902 Decastell and Sturil recognized AB
 Principle:
 Human red blood cells has A &/or B antigen
 They will agglutinate in presence of antibody directed to respective antigens
 The antibodies used for testing are monoclonal IgM produced by murine hydridoma
cell lines grown in tissue culture
 Each hybridoma cell produces single antibody
 Agglutination of red cells with anti A monoclonal and anti B monoclonal is positive it
indicates presence of corresponding antigen
 Absence of agglutination of red blood cell is negative result indicating absence of
corresponding antigen

HUMAN BLOOD GROUP

 It is based on the antigenic characters of red cells


 Presence or absence of antigen on red cells or the presence of antibodies in the plasma
indicates the persons blood group
 There are nearly 300 blood group systed
 The first to be discovered was ABO by Karl Landsteiner
 There are two types of blood group

1. Natural – there is natural presence of antibodies from birth which lack the
corresponding antigen on the RBC e.g ABO, MNS, P, LEWIS (Le) LUTHERN (Lu)
2. Immune blood group- these antigens are bale to produce immune antibodies in
receipients blood when exposed to them as foreign antigens e.g. Rh, Kidd (JK), Duffy
(F), Kell (K) etc
 Variation in blood group is due to different combination of antigens and
degree of dominance

ABO blood group system:

 It is the basic blood group system


 It is important because of the natural presence of A and B antibodies in persons
from birth who lack corresponding antigens on his red cells
 Transfusion of incompatible ABO blood group causes serious problems in
persons
 A,B antigens are detected on foetal red cells but receptor sites are not well
developed so the reactions are not strong
 A antigen exists as A1 which is strong reacting and A2 which is weak
 Infants have A2 at birth which becomes A1 later
 The antibodies to antigen other than those present are present naturally i.e. anti A
and anti B

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 They are IgM , a polyvalent antibodies


 It cant cross placenta that protects fetus from mothers incompatible natural
antibodies
 Antibodies A and B appear at the age of 3 to 4 months
 It increases at adolescence and declines with aging
 Anti a titer is higher than anti B
 Anti a titer is higher in O than in B group persons
 phenotypes of ABO blood group are of 6 types :- A1A2, B, A1B, A2B, and O
 subgroups are important for blood transfusion

Variations in ABO:

 Sometimes O has only anti B due to weak or abnormal A antigen on RBC or vice-
versa
 A, AB, B, blood group develop weak anti H so O blood group which has H
antigen cannot be received
 Bombay blood group Oh has anti H, anti A and anti B so cant accept O blood
group
 Bombay blood group lacks A,B,H antigens
 H antigen is present on RBC of all ABO blood groups
 In autoimmune anemia disease antibodies corresponding to antigens on rbc are
present
 Some plant products have properties like anti A, anti B and anti H
 These are lectins e.g.Dolichous biflorus

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Rh blood group system

 It is clinically important
 Rh negative persons if transfused with Rh positive blood, they form Rh
antibodies
 Haemolytic disease of newborn occurs due to Rh incompatibility of mothe –Rh
negative and fetus –Rh positive i.e. erythroblastofaetalis diseases
 Rh antigens are inherited
 anti Rh develop in Rh negative persons when he receive Rh positive RBC
 Landsteiner and Weiner transfused the red cells of rhesus monkey (Rh) into rabbit

 Rabbit produced anti Rh that could agglutinate rbc of rhesus monkey and of
human RBC
 They were called as Rh positive persons
 If RBC did not react with rabbit anti Rh sera then they are Rh negative
 If Rh (D) antigen is present on RBC then he is Rh positive
 So person of any ABO blood group can be Rh positive or Rh negative
 Inheritance of Rh antigen is independent of ABO antigens
 There are 110 antigen of Rh blood group of which 5 are important
 2 types of nomenclatures are used:-

Fisher-Race (easy to follow so is used) Wiener


D Rho
C Rh’
E Rh”
d Hr’
c Hr”

 Rh blood group has 5 linked allelic genes –Cc,D, Ee


 If D is present then he is Rh positive if absent then Rh negative

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Rh antibodies

 They are immune antibodies


 It is IgG
 Its molecular weight is 1,70,000
 It is monovalent and incomplete and can cross placenta
 So they cause heamolytic disease of new born in Rh negative mother bearing Rh
positive foetus
 Optimum reaction is 37oC

Rh variant (Du)

 These are weak D antigen


 It can be detected by Coombs test by using antihuman globin
 Same antigens are present on leukocytes, platelets and tissue cells e.g. human
leukocyte antigen (HLA) system
 HLA are present on all nucleated body cells so are important for organ transplantation

Importance of blood grouping:

 It is important for blood transfusion


 Identical ABO blood group of donor is ideal
 blood group is universal donor as they have no antigens on their RBC so they do not
react with corresponding antibodies
 AB blood group is universal recipient and can accept A, B, AB ,O as anti A and anti
B are absent
 Whole blood is given in case of heavy blood loss 9haenorrhage)
 Whole blood is not given to anemic persons as volume of blood increases
(hypervolumic) causing congestive heart failure
 They are given required packed red cells

How to detect your blood group…………….

Sample:

 Blood collected with or without anticoagulant may be used


 Test at the earliest
 Store samples at 2-8 C if delayed
 Blood got by finger puncture is tested by slide method
 Avoid clotting
 Store reagents at 2-8 C
 Avoid contamination
 Bring reagents to 25 C

Procedure:

 Rapid slide test:


 Prepare 10% suspension of RBC in normal slain (0.85% NaCl solution)

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 Oxalatedd whole blood can be used


 Mark three areas on glass slide as A and B
 Add one drop of corresponding reagent to the above areas
 Add one drop of cell suspension or whole blood to each of labeled areas
 With separate applicator sticks mix each cell reagent well
 Tilt slide back and forth
 Within 2 minutes, Observe macroscopic or microscopic agglutination

Interpretation

1. agglutination of red blood cells by reagent indicates positive result


2. absence of agglutination of red blood cells by reagent indicates negative result

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