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Alloimmunization and autoimmunization in transfusion dependent thalassemia major patients: Study on 319 patients
BACKGROUND: The development of anti-red blood cell antibodies (both allo-and autoantibodies) remains a major problem in thalassemia major patients. We studied the frequency of red blood cell (RBC) alloimmunization and autoimmunization among thalassemia patients who received regular transfusions at o...
Autores principales: | , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Medknow Publications & Media Pvt Ltd
2014
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4140069/ https://www.ncbi.nlm.nih.gov/pubmed/25161344 http://dx.doi.org/10.4103/0973-6247.137438 |
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author | Dhawan, Hari Krishan Kumawat, Vijay Marwaha, Neelam Sharma, Ratti Ram Sachdev, Suchet Bansal, Deepak Marwaha, Ram Kumar Arora, Satyam |
author_facet | Dhawan, Hari Krishan Kumawat, Vijay Marwaha, Neelam Sharma, Ratti Ram Sachdev, Suchet Bansal, Deepak Marwaha, Ram Kumar Arora, Satyam |
author_sort | Dhawan, Hari Krishan |
collection | PubMed |
description | BACKGROUND: The development of anti-red blood cell antibodies (both allo-and autoantibodies) remains a major problem in thalassemia major patients. We studied the frequency of red blood cell (RBC) alloimmunization and autoimmunization among thalassemia patients who received regular transfusions at our center and analyzed the factors, which may be responsible for development of these antibodies. MATERIALS AND METHODS: The study was carried out on 319 multiply transfused patients with β-thalassemia major registered with thalassemia clinic at our institute. Clinical and transfusion records of all the patients were examined for age of patients, age at initiation of transfusion therapy, total number of blood units transfused, transfusion interval, status of splenectomy or other interventions. Alloantibody screening and identification was done using three cell and 11 cell panel (Diapanel, Bio-rad, Switzerland) respectively. To detect autoantibodies, autocontrol was carried out using polyspecific coombs (IgG + C3d) gel cards. RESULTS: Eighteen patients out of total 319 patients (5.64%) developed alloantibodies and 90 (28.2%) developed autoantibodies. Nine out of 18 patients with alloantibodies also had autoantibodies. Age at first transfusion was significantly higher in alloimmunized than non-immunized patients (P = 0.042). Out of 23 alloantibodies, 52.17% belonged to Rh blood group system (Anti-E = 17%, Anti D = 13%, Anti-C = 13%, Anti-C(w) = 9%), 35% belonged to Kell blood group system, 9% of Kidd and 4% of Xg blood group system. CONCLUSION: Alloimmunization was detected in 5.64% of multitransfused thalassemia patients. Rh and Kell blood group system antibodies accounted for more than 80% of alloantibodies. This study re-emphasizes the need for RBC antigen typing before first transfusion and issue of antigen matched blood (at least for Rh and Kell antigen). Early institution of transfusion therapy after diagnosis is another means of decreasing alloimmunization. |
format | Online Article Text |
id | pubmed-4140069 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2014 |
publisher | Medknow Publications & Media Pvt Ltd |
record_format | MEDLINE/PubMed |
spelling | pubmed-41400692014-08-26 Alloimmunization and autoimmunization in transfusion dependent thalassemia major patients: Study on 319 patients Dhawan, Hari Krishan Kumawat, Vijay Marwaha, Neelam Sharma, Ratti Ram Sachdev, Suchet Bansal, Deepak Marwaha, Ram Kumar Arora, Satyam Asian J Transfus Sci Original Article BACKGROUND: The development of anti-red blood cell antibodies (both allo-and autoantibodies) remains a major problem in thalassemia major patients. We studied the frequency of red blood cell (RBC) alloimmunization and autoimmunization among thalassemia patients who received regular transfusions at our center and analyzed the factors, which may be responsible for development of these antibodies. MATERIALS AND METHODS: The study was carried out on 319 multiply transfused patients with β-thalassemia major registered with thalassemia clinic at our institute. Clinical and transfusion records of all the patients were examined for age of patients, age at initiation of transfusion therapy, total number of blood units transfused, transfusion interval, status of splenectomy or other interventions. Alloantibody screening and identification was done using three cell and 11 cell panel (Diapanel, Bio-rad, Switzerland) respectively. To detect autoantibodies, autocontrol was carried out using polyspecific coombs (IgG + C3d) gel cards. RESULTS: Eighteen patients out of total 319 patients (5.64%) developed alloantibodies and 90 (28.2%) developed autoantibodies. Nine out of 18 patients with alloantibodies also had autoantibodies. Age at first transfusion was significantly higher in alloimmunized than non-immunized patients (P = 0.042). Out of 23 alloantibodies, 52.17% belonged to Rh blood group system (Anti-E = 17%, Anti D = 13%, Anti-C = 13%, Anti-C(w) = 9%), 35% belonged to Kell blood group system, 9% of Kidd and 4% of Xg blood group system. CONCLUSION: Alloimmunization was detected in 5.64% of multitransfused thalassemia patients. Rh and Kell blood group system antibodies accounted for more than 80% of alloantibodies. This study re-emphasizes the need for RBC antigen typing before first transfusion and issue of antigen matched blood (at least for Rh and Kell antigen). Early institution of transfusion therapy after diagnosis is another means of decreasing alloimmunization. Medknow Publications & Media Pvt Ltd 2014 /pmc/articles/PMC4140069/ /pubmed/25161344 http://dx.doi.org/10.4103/0973-6247.137438 Text en Copyright: © Asian Journal of Transfusion Science http://creativecommons.org/licenses/by-nc-sa/3.0 This is an open-access article distributed under the terms of the Creative Commons Attribution-Noncommercial-Share Alike 3.0 Unported, which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited. |
spellingShingle | Original Article Dhawan, Hari Krishan Kumawat, Vijay Marwaha, Neelam Sharma, Ratti Ram Sachdev, Suchet Bansal, Deepak Marwaha, Ram Kumar Arora, Satyam Alloimmunization and autoimmunization in transfusion dependent thalassemia major patients: Study on 319 patients |
title | Alloimmunization and autoimmunization in transfusion dependent thalassemia major patients: Study on 319 patients |
title_full | Alloimmunization and autoimmunization in transfusion dependent thalassemia major patients: Study on 319 patients |
title_fullStr | Alloimmunization and autoimmunization in transfusion dependent thalassemia major patients: Study on 319 patients |
title_full_unstemmed | Alloimmunization and autoimmunization in transfusion dependent thalassemia major patients: Study on 319 patients |
title_short | Alloimmunization and autoimmunization in transfusion dependent thalassemia major patients: Study on 319 patients |
title_sort | alloimmunization and autoimmunization in transfusion dependent thalassemia major patients: study on 319 patients |
topic | Original Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4140069/ https://www.ncbi.nlm.nih.gov/pubmed/25161344 http://dx.doi.org/10.4103/0973-6247.137438 |
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