Figure 1.
Adsorption procedure to remove WAA using allogeneic RBCs. Example of the multistep process for allogeneic adsorptions to remove WAA to identify whether an underlying alloantibody is present (eg, anti-Jka). Three donor RBCs of known phenotypes (ie, R1R1, R2R2, and rr) are selected and treated with enzyme or ZZAP. The patient's serum (or plasma) is added to an aliquot of each of the 3 donor RBCs and incubated for 10 to 60 minutes at 37 °C. Three separate adsorptions are performed, each undergoing 1 to 4 rounds of adsorption in which the patient's serum is repeatedly incubated with a new set of donor RBCs. Following an adequate number of adsorptions, adsorbed serum samples are tested against reagent RBCs. If 1 or more aliquots are positive, an alloantibody can be identified based on the pattern of reactivity and knowledge of the antigens expressed on each aliquot of donor RBCs used for adsorption.

Adsorption procedure to remove WAA using allogeneic RBCs. Example of the multistep process for allogeneic adsorptions to remove WAA to identify whether an underlying alloantibody is present (eg, anti-Jka). Three donor RBCs of known phenotypes (ie, R1R1, R2R2, and rr) are selected and treated with enzyme or ZZAP. The patient's serum (or plasma) is added to an aliquot of each of the 3 donor RBCs and incubated for 10 to 60 minutes at 37 °C. Three separate adsorptions are performed, each undergoing 1 to 4 rounds of adsorption in which the patient's serum is repeatedly incubated with a new set of donor RBCs. Following an adequate number of adsorptions, adsorbed serum samples are tested against reagent RBCs. If 1 or more aliquots are positive, an alloantibody can be identified based on the pattern of reactivity and knowledge of the antigens expressed on each aliquot of donor RBCs used for adsorption.

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