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Human leukocyte antigen class I (A, B and C) allele and haplotype variation in a South African Mixed ancestry population

South Africa has a large (∼53 million), ethnically diverse population (black African, Caucasian, Indian/Asian and Mixed ancestry) and a high disease burden (particularly HIV-1 and Mycobacterium tuberculosis). The Mixed ancestry population constitutes ∼9% of the total population and was established ∼...

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Detalles Bibliográficos
Autores principales: Loubser, Shayne, Paximadis, Maria, Tiemessen, Caroline T.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Elsevier/North-Holland 2017
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5451074/
https://www.ncbi.nlm.nih.gov/pubmed/28438553
http://dx.doi.org/10.1016/j.humimm.2017.04.006
Descripción
Sumario:South Africa has a large (∼53 million), ethnically diverse population (black African, Caucasian, Indian/Asian and Mixed ancestry) and a high disease burden (particularly HIV-1 and Mycobacterium tuberculosis). The Mixed ancestry population constitutes ∼9% of the total population and was established ∼365 years ago in the Western Cape region through interracial mixing of black Africans, Europeans and Asians. Admixed populations present unique opportunities to identify genetic factors involved in disease susceptibility. Since HLA genes are important mediators of host immunity, we investigated HLA-A, -B and -C allele and haplotype diversity in 50 healthy, unrelated individuals recruited from the Mixed ancestry population.