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A comprehensive human leukocyte antigen analysis of 36 782 cord blood units stored in the Australian Public Cord Blood Banking Network
Affiliation:1. Sydney Cord Blood Bank, Sydney Children''s Hospital, Randwick, NSW, Australia;2. School of Women''s and Children''s Health, Faculty of Medicine, University of New South Wales, Randwick, NSW, Australia;3. Bone Marrow Transplant Laboratory, Randwick Hospitals, NSW Health Pathology, Randwick, NSW, Australia;4. Queensland Cord Blood Bank at the Mater, Mater Hospital, Raymond Terrace, Queensland, Australia;5. BMDI Cord Blood Bank, Murdoch Children''s Research Institute, Royal Children''s Hospital, Parkville, Victoria, Australia;6. Department of Paediatrics, University of Melbourne, Parkville, Victoria, Australia
Abstract:Background and aimsThe network of public cord blood banks (CBBs) in Australia, known as AusCord, comprises CBBs located in Brisbane, Sydney and Melbourne. A novel comprehensive analysis has been performed to determine whether the cryopreserved, searchable cord blood unit (CBU) inventory of approximately 36 000 units share similar tissue types or haplotypes.MethodsHuman leukocyte antigen (HLA) data was analysed using Microsoft Excel following standardisation of typing data.ResultsThe analysis has found that the majority of stored, searched and released CBU exhibit a tissue type that is unique within and between the CBBs. Therefore, each collection performed by the CBBs is likely to comprise a tissue type that is not already stored among the total AusCord inventory. HLA alleles (HLA-A*34, HLA-B*56, HLA-DRB1*08:03), which are uncommon in European populations, were associated with Pacific Islander and/or Indigenous Australian populations and confirmed to be more frequent among donors who, when screened, self-identified as these ethnicities.ConclusionsThese data indicate that (i) continued addition of CBU to existing inventories is likely to further increase the HLA diversity and (ii) screening donors for ethnicity or strategically locating collection sites where ethnic minorities reside can successfully result in collection of rare HLA associated with ethnic minority groups for whom finding donors might otherwise be more difficult.
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