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Changes of isoagglutinin titres after ABO-incompatible allogeneic stem cell transplantation
Authors:Lee Je-Hwan  Lee Jung-Hee  Choi Seong-Jun  Kim Shin  Seol Miee  Kwon Seog-Woon  Park Chan-Jeoung  Chi Hyun-Sook  Lee Jung-Shin  Kim Woo-Kun  Lee Kyoo-Hyung
Affiliation:Department of Medicine, Asan Medical Centre, University of Ulsan, Seoul, Korea. jhlee3@www.amc.seoul.kr
Abstract:We investigated the changes in isoagglutinin titres in 62 patients who underwent ABO-incompatible allogeneic stem cell transplantation. After major [and/or (+/-) minor] ABO-incompatible transplantation, recipient-derived isoagglutinins against donor-type red blood cells (RBCs) disappeared more rapidly in unrelated recipients (P = 0.006) and in patients with acute graft-versus-host disease (GVHD, P = 0.025) than in sibling recipients and in patients without acute GVHD respectively. Pure red cell aplasia (PRCA) developed in 10 out of 35 evaluable patients who underwent major (+/- minor) ABO-incompatible transplantation, and the post-transplant increase of isoagglutinin titres was a significant predictor for the occurrence of PRCA. In five out of 36 patients who underwent minor (and/or (+/-) major) ABO-incompatible transplantation, donor-derived isoagglutinins against recipient RBCs were detectable without clinically overt haemolysis. Isoagglutinin titres against ABO antigens absent both on recipient and donor RBCs decreased during the early post-transplant period then rose subsequently in 24 out of 29 patients at (median) d 59 post transplant. Our study showed that changes in isoagglutinin titres might have clinical implications in the occurrence of immunohaematological complications such as PRCA or immune-mediated haemolysis, and might reflect immunohaematological reconstitution after transplantation. Furthermore, our data regarding time to disappearance of recipient-derived isoagglutinins against donor-type RBCs after major ABO-incompatible transplantation suggest the presence of a graft-versus-plasma cell effect.
Keywords:ABO incompatibility    stem cell transplantation    PRCA    graft-versus-plasma cell effect    immunohaematological reconstitution
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