The HLA-DRB1*11 group-specific allele is a predictor for alloantibody production in the transfusion-dependent thalassemia patients

被引:8
作者
Ebrahimi, Mina [1 ,2 ]
Maleknia, Mohsen [1 ,2 ]
Parav, Nastaran [3 ]
Mohammadi, Mohammad Bagher [1 ,2 ]
Mortazavi, Yousef [4 ]
Saki, Najmaldin [1 ]
Rahim, Fakher [1 ,5 ]
机构
[1] Ahvaz Jundishapur Univ Med Sci, Thalassemia & Hemoglobinopathy Res Ctr, Hlth Res Inst, Ahvaz, Iran
[2] Ahvaz Jundishapur Univ Med Sci, Student Res Comm, Ahvaz, Iran
[3] Ahvaz Jundishapur Univ Med Sci, Reference Lab, Ahvaz, Iran
[4] Zanjan Univ Med Sci, Canc Gene Therapy Res Ctr, Zanjan, Iran
[5] Ahvaz Jundishapur Univ Med Sci, Clin Res Dev Unit, Golestan Hosp, Ahvaz, Iran
关键词
Alloimmunization; Thalassemia; HLA-DRB1; HLA-DRB1*13; HLA-DRB1*11; BLOOD-CELL ALLOIMMUNIZATION; HLA-DRB1; HLA;
D O I
10.1016/j.transci.2020.102729
中图分类号
R5 [内科学];
学科分类号
1002 ; 100201 ;
摘要
Background and Objectives: Recently, researchers have shown an increased interest in thalassemia for detecting susceptible factors in alloimmunization development. Alloimmunization, especially against Rh and Kell blood, occurs in 30% of thalassemia dependent transfusion (TDT) patients. The aim of this study is to determine the role of HLA-DRB1*11 and HLA-DRB1*13 group-specific alleles in the production of Rh and Kell alloantibodies. Materials and Methods: 106 TDT patients were recruited for this study (54 responders and 52 non-responders). Responder patients developed Rh, Kell and/or specificities alloantibodies. HLA genotyping was done with Sequence-Specific Primers (SSP-PCR) and the results were compared between two groups. Results: A significant association was found between anti-K (P=0.021, OR=2.546, 95%CI) and anti-E (P=0.049, OR=2.304, 95%CI) alloantibodies production with DRB1*11, respectively. Development of Anti-K and Anti-E alloantibodies were associated with DRB1*11 (P=0.021, OR=2.546, 95%CI) (P=0.049, OR=2.304, 95%CI), respectively. Further analysis showed that DRB1*11 is more frequent in multi responders (responder with both Rh and Kell alloantibodies) than mono-responders, 71% Versus 29%. There was not found any association between the DRB1*13 group-specific allele and the production of alloantibodies (P=0.584, OR=0.308, 95%CI). Conclusions: The evidence from this study suggests that detecting the DRB1*11 group-specific allele before starting transfusion can be useful to identify susceptible patients, increase HSCT transplantation compatibility and blood transfusion management.
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页数:5
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