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Characterization of novel HLA-A*24:608N allele discovered in Koreans.
Jeong, In Hwa; Lee, Jong Kwon; Kwon, Won Kyung; Song, Eun Young; Kim, Kyeong-Hee; Lee, Jina; Jung, Sunmi; Jeong, Mijeong; Park, June-Woo; Kang, Eun Suk.
Afiliación
  • Jeong IH; Department of Laboratory Medicine and Genetics, Samsung Medical Center, Sungkyunkwan University School of Medicine, Seoul, South Korea.
  • Lee JK; Department of Laboratory Medicine, Dong-A University Hospital, Dong-A University College of Medicine, Busan, South Korea.
  • Kwon WK; Department of Laboratory Medicine and Genetics, Samsung Medical Center, Sungkyunkwan University School of Medicine, Seoul, South Korea.
  • Song EY; Department of Laboratory Medicine and Genetics, Samsung Medical Center, Sungkyunkwan University School of Medicine, Seoul, South Korea.
  • Kim KH; U2Labs, Jangwon Medical Foundation, Seoul, South Korea.
  • Lee J; Department of Laboratory Medicine, Seoul National University Hospital, Seoul National University, College of Medicine, Seoul, South Korea.
  • Jung S; Department of Laboratory Medicine, Dong-A University Hospital, Dong-A University College of Medicine, Busan, South Korea.
  • Jeong M; BioTide Co., Ltd., Seoul, South Korea.
  • Park JW; BioTide Co., Ltd., Seoul, South Korea.
  • Kang ES; Research Institute for Future Medicine, Samsung Medical Center, Sungkyunkwan University School of Medicine, Seoul, South Korea.
HLA ; 103(1): e15332, 2024 01.
Article en En | MEDLINE | ID: mdl-38174645
ABSTRACT
A novel null HLA-A*24 allele, HLA-A*24608N, 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.
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Texto completo: 1 Colección: 01-internacional Banco de datos: MEDLINE Asunto principal: Antígenos HLA-A / Secuenciación de Nucleótidos de Alto Rendimiento Tipo de estudio: Prognostic_studies Límite: Humans País/Región como asunto: Asia Idioma: En Revista: HLA Año: 2024 Tipo del documento: Article País de afiliación: Corea del Sur

Texto completo: 1 Colección: 01-internacional Banco de datos: MEDLINE Asunto principal: Antígenos HLA-A / Secuenciación de Nucleótidos de Alto Rendimiento Tipo de estudio: Prognostic_studies Límite: Humans País/Región como asunto: Asia Idioma: En Revista: HLA Año: 2024 Tipo del documento: Article País de afiliación: Corea del Sur