FCGR3B allele frequencies in Tunisians of sub-Saharan origin

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• 作者：M. Oueslati Belhaj Hassine^a ; ^b ; ^{oueslatimeriem@gmail.com} ; H. Ennafaa^b ; S. Kalai^a ; R. Kibech^a ; M.H. Sellami^a ; L. Bouzid^a ; S. Kaabi^a ; S. Abid^a
• 关键词：FCGR3B ; HNA ; Neutrophil ; North Africa ; Sub-Saharan Africa
• 刊名：Transfusion Clinique et Biologique
• 出版年：2012
• 期刊代码：249_12467820
• 类别：med
• 出版时间：April, 2012
• 卷：19
• 期：2
• 页码：60-63
• 文件大小：252 K

摘要

Purpose of the study

The importance of human neutrophil antigens (HNA) in immunogenetics and their involvement in hematologic diseases have accelerated the elucidation of their molecular basis and their allele frequencies distribution has been described in many populations over the world. In this study, our aim was to evaluate the frequency of FCGR3B alleles encoding HNA-1a, 1b and 1c among Tunisians of sub-Saharan origin and to compare them to Tunisian blood donors and to a group from sub-Saharan Africa.

Patients and methods

We typed the DNA of 106 individuals (62 Tunisians of sub-Saharan origin, 33 Tunisian blood donors and 11 from sub-Saharan Africa) for the three FCGR3B alleles by polymerase chain reaction using sequence specific primer (PCR-SSP).

Results

FCGR3B*1, FCGR3B*2 and FCGR3B*3 allele frequencies were respectively 0.347, 0.573 and 0.080 among Tunisians of sub-Saharan origin, 0.379, 0.591 and 0.030 among Tunisian blood donors and 0.318, 0.546 and 0.136 among the group from sub-Saharan Africa.

Conclusion

These allele frequencies were similar to those previously reported in other black and white populations. The frequencies found in the two Tunisian groups confirm the intermixing origin from Europe, sub-Africa and Asia of the Tunisian population. Our results provide a database for future studies of the HNA system and associated diseases in Tunisia.