Presentation on theme: "P RACTICAL A SPECTS OF R H G ROUPING Rh grouping in routine use for donors and patients involves testing for Rh (D) antigen only However tests for other."— Presentation transcript:
P RACTICAL A SPECTS OF R H G ROUPING Rh grouping in routine use for donors and patients involves testing for Rh (D) antigen only However tests for other important Rh antigens e.g. C,c,E and e may be done for Rh genotyping. The method of Rh grouping mainly depends on the type of reagents available, for which the manufacturers’ instructions have to be strictly followed.
R EAGENTS FOR R H (D) G ROUPING I Polyclonal human anti-D serum (IgG) Potentiating or enhancing substances such as albumin, enzymes and AHG reagent are used to bring about agglutination with human IgG anti-D. Anti-D serum (IgG) for saline or rapid tube test (high protein medium) This contains macromolecular additives and give reliable results. Anti-D for saline tube test 2 types Anti-D IgM Anti-D IgG - Chemically modified
II M ONOCLONAL ANTIBODIES IgM anti-D monoclonal reagent IgM and IgG anti-D monoclonal reagent Blend of IgM monoclonal + IgG polyclonal reagent These antibodies are highly specific, react equally well at 20°C as well as 37°C and are reliable for slide and rapid test tube technique. IgM anti-D monoclonal reagent cannot be used for Du testing by indirect antiglobulin test (IAT) while IgM + IgG monoclonal reagent and blend of IgM monolconal and IgG polyclonal can be used for Du testing.
III C ONTROLS FOR R H (D) GROUPING Known 0 Rh (D) positive and 0 Rh (D) negative cells may be used as controls with monoclonal anti-D reagent. Alternatively, AB serum or diluents control provided with the anti-D reagent or 22% bovine serum albumin may be used as negative control with the test cells
R H (D) G ROUPING In most of the blood transfusion laboratories, Rh (D) grouping is performed along with the ABO grouping and same techniques as used for ABO grouping may also be employed for Rh typing
S LIDE T ECHNIQUE This technique may be used in emergency Rh (D) typing if a centrifuge is not available. The slide test is not recommended for routine test as it may not pick up weak reactions, thus giving negative results.
T UBE T ECHNIQUE a. Saline Agglutination test for Rh (13) Typing Procedure 1. Prepare 2-5% washed red cell suspension of test sample. 2. Place 1 drop of anti-D in cleaned tube labelled D. 3. Place 1 drop of 22% bovine albumin/control reagent in another tube labelled C. 4. Add 1 drop of 2-5% test cell suspension to each tube. 5. Mix well and centrifuge at 1000 rpm for 1 minute (in case of using IgG anti-D, incubate at 37°C for 10mm. and centrifuge (spin tube method) or incubate at 37°C for 60 minutes (sedimentation method). 6. Resuspend the cell button and look for agglutination. All negative results must be confirmed under microscope
Interpreation Positive test : Agglutination in anti-D and smooth suspension in control tube. Negative test : Smooth suspension in all the tubes (test and control) Test is considerable invalid if both test and control tubes show a positive reaction. In such case, the test should be repeated using saline IgM anti-D. For all microscopically negative reactions in donor grouping, Du testing should be performed, hereas some workers suggest that if the two anti D reagents used are potent and specific, it is not necessary to perform Du testing. T UBE T ECHNIQUE
A LBUMIN TECHNIQUE FOR R H (D) TYPING Principle Albumin increases the dielectric constant of the medium and thus reduces the zeta potential. Due to this effect, the electrical repulsion between the red blood cells is less and the cells agglutinate. Mostly 22% bovine albumin is used, as higher concentrations can cause rouleaux formation.
E NZYME AGGLUTINATION TECHNIQUE FOR R H (D) TYPING Proteolytic enzymes such as papain, trypsin, bromelain and ficin digest the cell membrane partially and expose Rh antigens to react with IgG antibodies. When the membrane is partially removed, it brings about a loss of negative electric charge on the red cell which is responsible for keeping the cells a set distance apart, hence small IgG molecules are able to span the gap between cells and bring about agglutination.
R H (D) G ROUPING I N H AEMOLYTLC D ISEASE OF THE N EWBORN In haemolytic disease of the newborn, the baby’s red cells may be coated with immunoglobulin and a saline reactive Rh antiserum is usually necessary for testing. When the cells are heavily coated with antibody, no free antigenic sites remain for reaction, resulting in a negative test. This is suspected when the infant’s cells show a positive direct antiglobulin test (DAT) and a negative test with anti-D reagent. In such instances it is recommended that the antibody should be eluted by gentle elution (heating at 45°C for 30 minutes) to expose the antigenic sites before testing.
R H D ISCREPANCIES Rh –ve persons mistyped, & transfused with Rh +ve blood have 70% chance of becoming immunized False +ve reactions can be identified by testing an Rh control with the patient’s red cells each time an Rh typing is performed
C AUSES OF FALSE POSITIVE REACTIONS 1. Positive direct antiglobulin test 2. Polagglutinable red cells 3. Cold agglutinins or Rouleaux formation
1- P OSITIVE DIRECT ANTIGLOBULIN TEST The presence of Ab on patient’s red cells can cause a false +ve reaction with slide and tube anti-D High protein medium reduces zeta potential allowing red cells to move closer The cell bound Ab can cross link cells and cause agglutination
2- P OLAGGLUTINABLE RED CELLS Rh –ve red cells that are polyagglutinable due to T or Tn activation Agglutination occurs if anti-T or anti-Tn present in the anti-D reagent Most anti-D reagents do not contain these antibodies
3- C OLD AGGLUTININS OR R OULEAUX FORMATION Rh typing is performed using serum suspended red cells If individual’s serum contains cold agglutinin or abnormal protein, false positive reactions can occur
F ALSE N EGATIVES False negatives are not readily identifiable, but can occur in the following instances: The most common is the result of too heavy cell suspension due to too many cells for the amount of antibody in the antisera. They may also rarely be caused by extremely strong positive DAT. In this case a the patient's D antigen sites are coated in vivo and there are no sites left for commercial anti-D to attach to. This can be fixed by heating cells gently to elute off antibody without damaging cells, then re-test.
R ESOLVING R H P ROBLEMS Erroneous Results in Rh Grouping 1. Perform clerical checks for validity of labels and requisition forms. 2. Obtain a fresh blood sample of patient. 3. Check patient rçcords for history, diagnosis, pregnancy, medication and previous transfusion. 4. Check equipment and reagents for proper quality control. 5. Check the antisera and controls. 6. Perform alternative procedures such as washing of red cells with warm saline, enzyme treatment of red cells, absorption / elution studies. 7. Carry out family studies.