Human neutrophil antigen profiles in Banjar, Bugis, Champa, Jawa and Kelantan Malays in Peninsular Malaysia

• Published in: Blood transfusion = Trasfusione del sangue Vol. 13; no. 4; pp. 610 - 615
• Main Authors: Manaf, Siti M, NurWaliyuddin, Hanis Z A, Panneerchelvam, Sundararajulu, Zafarina, Zainuddin, Norazmi, Mohd N, Chambers, Geoffrey K, Edinur, Hisham A
• Format: Journal Article
• Language: English
• Published: Italy Edizioni SIMTI - SIMTI Servizi Srl 01.10.2015
• Subjects: Acute Lung Injury - epidemiology; Acute Lung Injury - etiology; Acute Lung Injury - immunology; Alleles; Ethnic Groups - genetics; Female; Gene Frequency; Genotype; Humans; Isoantibodies - biosynthesis; Isoantibodies - immunology; Isoantigens - analysis; Isoantigens - genetics; Malaysia - epidemiology; Male; Neutropenia - epidemiology; Neutropenia - immunology; Neutrophils - immunology; Original; Polymerase Chain Reaction; Polymorphism, Restriction Fragment Length; Pregnancy; Risk; Transfusion Reaction
• ISSN: 1723-2007
• DOI: 10.2450/2015.0278-14

Human neutrophil antigens (HNA) are polymorphic and immunogenic proteins involved in the pathogenesis of neonatal alloimmune neutropenia, transfusion-related acute lung injury (TRALI) and transfusion-related alloimmune neutropenia. The characterisation of HNA at a population level is important for predicting the risk of alloimmunisation associated with blood transfusion and gestation and for anthropological studies. Blood samples from 192 healthy, unrelated Malays were collected and genotyped using polymerase chain reaction-sequence specific primers (HNA-1, -3, -4) and polymerase chain reaction-restriction fragment length polymorphisms (HNA-5). The group comprised 30 Banjar, 37 Bugis, 51 Champa, 39 Jawa and 35 Kelantan Malays. The most common HNA alleles in the Malays studied were HNA-1a (0.641-0.765), -3a (0.676-0.867), -4a (0.943-1.000) and -5a (0.529-0.910). According to principal coordinate plots constructed using HNA allele frequencies, the Malay sub-ethnic groups are closely related and grouped together with other Asian populations. The risks of TRALI or neonatal neutropenia were not increased for subjects with HNA-1, -3 and -4 loci even for donor and recipient or pairs from different Malay sub-ethnic groups. Nonetheless, our estimates showed significantly higher risks of HNA alloimmunisation during pregnancy and transfusion between Malays and other genetically differentiated populations such as Africans and Europeans. This study reports HNA allele and genotype frequencies for the five Malay sub-ethnic groups living in Peninsular Malaysia for the first time. These Malay sub-ethnic groups show closer genetic relationships with other Asian populations than with Europeans and Africans. The distributions of HNA alleles in other lineages of people living in Malaysia (e.g. Chinese, Indian and Orang Asli) would be an interesting subject for future study.