Literature DB >> 3279575

Immunohematologic consequences of major ABO-mismatched bone marrow transplantation.

I J Sniecinski1, L Oien, L D Petz, K G Blume.   

Abstract

Twelve of 58 (21%) evaluable patients of blood group 0 who received a bone marrow transplant (BMT) from an HLA-matched sibling of a donor of group A or B developed significant immunohematologic problems in the posttransplant period. Anti-A or anti-B isohemagglutinins persisted for longer than 120 days post-BMT in nine patients and are still present in three patients at days +162 to +605. Red cell production as indicated by a reticulocyte count of greater than 0.5% was delayed to 40 days or more in nine patients, and in five of these was markedly delayed to 170 days or longer. One patient does not as yet have red cell production on day +605 in spite of having had 13 plasma exchanges performed to reduce the anti-B titer. Five patients experienced overt hemolysis, manifested by a sudden drop in hemoglobin of 1.5 to 4 gm/dl (median = 2.5 mg/dl), starting on day +37 to +105 (median = +65), persisting for 10 to 94 days (median = 36 days). Hemolysis and a delay in the onset of erythropoiesis beyond 170 days were more frequent in 30 patients treated with cyclosporine/prednisone than in 28 patients treated with methotrexate/prednisone for graft-versus-host disease prophylaxis. Our data indicate that ABO major mismatched BMT can be associated with significant immunohematologic consequences, some of which occur more frequently in association with cyclosporine administration.

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Year:  1988        PMID: 3279575     DOI: 10.1097/00007890-198803000-00005

Source DB:  PubMed          Journal:  Transplantation        ISSN: 0041-1337            Impact factor:   4.939


  7 in total

Review 1.  Transfusion Support for ABO-Incompatible Progenitor Cell Transplantation.

Authors:  Patricia M Kopko
Journal:  Transfus Med Hemother       Date:  2015-10-29       Impact factor: 3.747

Review 2.  Pure red cell aplasia after major or bidirectional ABO incompatible hematopoietic stem cell transplantation: to treat or not to treat, that is the question.

Authors:  Javier Marco-Ayala; Inés Gómez-Seguí; Guillermo Sanz; Pilar Solves
Journal:  Bone Marrow Transplant       Date:  2020-11-14       Impact factor: 5.483

3.  Impact of ABO blood group mismatch in alemtuzumab-based reduced-intensity conditioned haematopoietic SCT.

Authors:  C K Brierley; T J Littlewood; A J Peniket; R Gregg; J Ward; A Clark; A Parker; R Malladi; P Medd
Journal:  Bone Marrow Transplant       Date:  2015-04-13       Impact factor: 5.483

4.  Prevention of pure red cell aplasia after major or bidirectional ABO blood group incompatible hematopoietic stem cell transplantation by pretransplant reduction of host anti-donor isoagglutinins.

Authors:  Georg Stussi; Jörg Halter; Eveline Bucheli; Piero V Valli; Lutz Seebach; Jürg Gmür; Alois Gratwohl; Urs Schanz; Jakob R Passweg; Jörg D Seebach
Journal:  Haematologica       Date:  2009-01-14       Impact factor: 9.941

5.  Blood transfusion in marrow graft recipients.

Authors:  P Pihlstedt; T Paulin; B Sundberg; B Nilsson; O Ringdén
Journal:  Ann Hematol       Date:  1992-08       Impact factor: 3.673

6.  VH1 Family Immunoglobulin Repertoire Sequencing after Allogeneic Hematopoietic Stem Cell Transplantation.

Authors:  Maya K Sethi; Felicitas Thol; Michael Stadler; Michael Heuser; Arnold Ganser; Christian Koenecke; Oliver Pabst
Journal:  PLoS One       Date:  2017-01-17       Impact factor: 3.240

7.  The outcomes of hypertransfusion in major ABO incompatible allogeneic stem sell transplantation.

Authors:  Se Hoon Park; Mark Hong Lee; Se Hoon Lee; Kyung-Eun Lee; Jinny Park; Joon Oh Park; Kihyun Kim; Won Seog Kim; Chul Won Jung; Young-Hyuk Im; Won Ki Kang; Keunchil Park; Seon Woo Kim; Kyoo Hyung Lee; Je Hwan Lee
Journal:  J Korean Med Sci       Date:  2004-02       Impact factor: 2.153

  7 in total

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