Practical Blood Bank Antibody Titration Principle Titration is

Practical Blood Bank Antibody Titration

Principle Titration is a semi quantitative method used to determine the concentration of antibody in a serum sample or to compare the strength of antigen expression on different red cell samples. The usual applications of titration studies are: 1. Estimating antibody activity in alloimmunized pregnant women to determine whether and when to perform more complex invasive investigation of the fetal condition. 2. characterizing antibodies as high-titer, low-avidity 3. Observing the effect of sulfhydryl reagents on antibody behavior, to determine immunoglobulin class (Ig. G or Ig. M).

Titration in pregnant women q q Titration studies specifically to assist in monitoring clinically significant antibodies in the pregnant woman. When the titer (eg, >16) and the antibody specificity have been associated with HDFN, it is recommended that repeat titration studies be performed every 2 to 4 weeks, beginning at 18 weeks’ gestation; save an aliquot of the serum (frozen at – 20 C or colder) for comparative studies with the next submitted sample.

characterizing antibodies as high-titer, low-avidity Speed and strength of agglutination is termed as avidity. The test is done by mixing two drop of anti-serum with one drop of 40 -50% cell suspension on a slide or cover and rocking gently at room temperature (RT). The time for a clearly visible reaction (+1) and then for strong (+4) reaction to occur are recorded with the help of stop watch.

Observing the effect of sulfhydryl reagents on antibody behavior, to determine immunoglobulin class (Ig. G or Ig. M).

Specimen Serum for titration (containing potentially significant unexpected antibodies to red cell antigens, 1 m. L). If possible, test the current sample in parallel with the most recent previously submitted (preceding) sample from the current pregnancy.

Materials 1. Antihuman Ig. G: need not be heavy chain- specific. 2. Isotonic saline. 3. Volumetric pipettes, or equivalent: 0. 1 - to 0. 5 -m. L delivery, with disposable tips. 4. Red cells: group O reagent red cells, 2% suspension. (See note 1 regarding the selection of red cells for testing. ) Avoid using Bg+ red cells because they may result in falsely high values, especially with sera from multi-parous women. 5. Ig. G-coated red cells.

Procedure 1. Using 0. 5 -m. L volumes, prepare serial twofold dilutions of serum in saline. The initial tube should contain undiluted serum and the doubling dilution range should be from 1 in 2 to 1 in 2048 (total of 12 tubes). 2. Place 0. 1 m. L of each dilution into appropriately labeled test tubes. 3. Add 0. 1 m. L of the 2% suspension of red cells to each dilution. Alternatively, for convenience, add 1 drop of a solution of a 3% to 4% suspension of red cells as supplied by the reagent manufacturer, although this method is less precise.

4. Gently agitate the contents of each tube; incubate at 37 C for 1 hour. 5. Wash the red cells four times with saline; completely decant the final wash supernatant. 6. To the dry red cell buttons thus obtained, add anti-Ig. G according to the manufacturer’s directions. 7. Centrifuge as for hemagglutination tests. 8. Examine the red cells macroscopically; grade and record the reactions. 9. Add Ig. G-coated red cells to all negative tests; recentrifuge and examine the tests for macroscopic agglutination; repeat the testing if the tests with Ig. Gcoated red cells are nonreactive.

Interpretation The titer is reported as the reciprocal of the highest dilution of serum at which 1+ agglutination is observed. A titer ≥ 16 (this value may vary according to the laboratory) is considered significant and may warrant further monitoring for HDFN.

Notes 1. The selection of the most suitable phenotype of red cells to use when performing titration studies for HDFN is controversial. ◦ Some workers select red cells that have the strongest expression of antigen, such as R 2 R 2 for anti-D. ◦ it is important that the laboratory be consistent and use red cells of the same phenotype for future titrations to test the same patient’s serum. 2. Titration studies should be performed upon initial detection of the antibody; save an appropriately labeled aliquot of the serum (frozen at – 20 C or colder) for comparative studies with the next submitted sample.

Notes 3. Do not use enhancement techniques [albumin, polyethylene glycol, low ionic strength saline (LISS)] or enzyme-treated red cells because falsely elevated titers may be obtained. Gel testing is not recommended. 4. LISS should not be used as a diluents in titration studies; nonspecific uptake of globulins may occur in serum-LISS dilutions. 5. Failure to obtain the correct results may be caused by q incorrect technique, notably, failure to use separate pipette tips for each dilution or q failure to adequately mix thawed frozen serum.

NOTES AND PRECAUTIONS If titrating anti-A, anti-B, or anti-A, B, the serologic technique is performed by the same method as ABO Typing If titrating Rh, Kell, Duffy, or Kidd antibodies, the serologic technique includes a 37 o. C followed by antiglobulin testing. Prozone phenomenon may occur so the first tubes may have a weaker reaction than the more diluted serum. AABB recommends reading the most dilute tubes first and then shake out the other tubes.

GRADING OF AGGLUTINATION REACTION Grade Description +4 +4 Single clump of agglutination with no free cells +3 Three or four individual clumps with few free cells +2 +1 Many fairly large clumps with many free cells +W 2 to 3 cells sticking together per low power field, uneven distribution Visually no agglutination Fine granular appearance visually, but definite small clumps (10 -15 cells) per low power field - All cells are free H Hemolysis (partial or total) must be interpreted as positive

0 No agglutination or Hemolysis W+ to 1+ Tiny agglutinates turbid background Small agglutinates turbid background 2+ Medium-sized Agglutinates-Clear Background

3+ Several large agglutinates-Clear Background 4+ One Solid Agglutinate