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Red cell alloimmunization and autoantibodies in Egyptian transfusion-dependent thalassaemia patients

INTRODUCTION: The objective of this study was to explore the frequency of red cell alloantibodies and autoantibodies among β-thalassaemia patients who received regular transfusions. MATERIAL AND METHODS: This study included 501 patients with β-thalassaemia. This work planned to study the presence of...

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Detalles Bibliográficos
Autores principales: Ahmed, Azza Mohamed, Hasan, Nehal Salah, Ragab, Shadia Hassan, Habib, Sonia Adolf, Emara, Nahed Abdelmonem, Aly, Azza Ahmed
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Termedia Publishing House 2010
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3284076/
https://www.ncbi.nlm.nih.gov/pubmed/22371805
http://dx.doi.org/10.5114/aoms.2010.14473
Descripción
Sumario:INTRODUCTION: The objective of this study was to explore the frequency of red cell alloantibodies and autoantibodies among β-thalassaemia patients who received regular transfusions. MATERIAL AND METHODS: This study included 501 patients with β-thalassaemia. This work planned to study the presence of alloantibodies and autoantibodies to different red cell antigens in multitransfused thalassaemia patients using the ID. Card micro typing system. RESULTS: Of a total of 501 β-thalassaemia patients included in the study, 11.3% of patients developed alloantibodies; 9.7% of these alloantibodies were clinically significant. The most common alloantibodies were anti-K, anti-E and anti-C. The rate of incidence of these alloantibodies was 3.9%, 3.3% and 1.7% respectively. Autoantibodies occurred in 28.8% of the patients and 22.1% of these antibodies were typed IgG. There was a significant association between splenectomy with alloimmunization and autoantibody formation (p = 0.03, p = 0.001 respectively). There was no significant association between alloantibody, autoantibody formation and number of transfused packed red cells. CONCLUSIONS: Alloimmunization to minor erythrocyte antigens and erythrocyte autoantibodies of variable clinical significance are frequent findings in transfused β-thalassaemia patients. There is an association between absence of the spleen and the presence of alloimmunization and autoantibody formation.