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Characterization of novel HLA-A*24:608N allele discovered in Koreans.

In Hwa JeongJong Kwon LeeWon Kyung KwonEun Young SongKyeong-Hee KimJina LeeSunmi JungMijeong JeongJune-Woo ParkEun Suk Kang
Published in: HLA (2024)
A novel null HLA-A*24 allele, HLA-A*24:608N, was identified in five Korean subjects including three from a family and two separate individuals. This study was performed to discern its immunological function in transplantation settings. Because this null variant had deletions of approximately 12 k base pairs from intron 3 to 3' end of the HLA-A gene, low resolution HLA typing and amplicon-based next generation sequencing (NGS) typing methods had failed to assign it. Hybrid capture-based NGS method confirmed that this novel variant had a large deletion. T-lymphocyte crossmatching by complement-dependent lymphocytotoxicity and flow cytometry with a serum consisting anti-HLA-A24 antibody revealed negative results, implying that an individual with this allele would not carry a functioning A24 antigen. These findings highlight the importance of identifying a null HLA allele by employing appropriate molecular method and providing expected crossmatching outcomes in a real-world transplantation setting.
Keyphrases
  • flow cytometry
  • gene expression
  • type diabetes
  • metabolic syndrome
  • stem cells
  • genome wide
  • mesenchymal stem cells
  • peripheral blood
  • skeletal muscle