Identification of anti-Lea by platelet complement fixation

Vox Sang. 1986;50(3):169-73. doi: 10.1111/j.1423-0410.1986.tb04872.x.

Abstract

Two anti-Lea sera which were able to detect Lea antigen on platelets were identified in a screening for anti-platelet antibodies by means of a platelet complement fixation test. These two antisera hemolyzed erythrocytes without enzyme treatment. The anti-Lea activity could be completely absorbed by red cells, platelets and lymphocytes of Le(a+b-) donors but not by cells from Le(a-b+) or Le(a-b-) donors. The antibody activity against red cells was eliminated by treatment of the antisera with dithiothreitol, thereby suggesting that the activity resided in the IgM class of immunoglobulins. As the anti-Lea was more reactive at 37 degrees C than at room temperature against both red cells and platelets, we suggest that transfusion of platelets of Lea-negative donors should be considered for patients with this type of anti-Lea.

MeSH terms

  • Blood Platelets / immunology*
  • Complement Fixation Tests*
  • Hemolysis
  • Humans
  • Immune Sera
  • Indicator Dilution Techniques
  • Isoantibodies / analysis*
  • Lewis Blood Group Antigens / immunology*
  • Temperature

Substances

  • Immune Sera
  • Isoantibodies
  • Lewis Blood Group Antigens