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Human leukocyte antigen (HLA) is a group of glycoproteins encoded by the major histocompatibility complex (MHC) that plays a pivotal role in the host's immune defense. Given that the MHC represents the most polymorphic region in the human genome, HLA typing is crucial in organ transplantation. It significantly influences graft rejection, graft-versus-host disease, and the overall patient outcome by mediating the discrimination between self and nonself. HLA typing technology began with serological methods and has evolved rapidly alongside advances in molecular technologies, progressing from DNA-based typing to next- or third-generation sequencing. These advancements have increased the accuracy of HLA typing and reduced ambiguities, leading to marked improvements in transplantation outcomes. Additionally, numerous novel HLA alleles have been identified. In this review, we explore the developmental history and future prospects of HLA typing technology, which promises to further benefit the field of transplantation.
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http://dx.doi.org/10.4285/ctr.24.0055 | DOI Listing |
We identified seven novel HLA class I alleles by NGS.
View Article and Find Full Text PDFHum Immunol
September 2025
Department of Pathology, St. Jude Children's Research Hospital, Memphis, TN, USA. Electronic address:
Transfusion support for sensitized patients is an important function of blood centers and HLA laboratories. However, access to widely available software to facilitate matching patients with compatible donor units is limited. We developed vendor-supported and integrated software that interfaces with the laboratory informatics system, sourcing typing data from our platelet donor registry and retrieving patient HLA typing and unacceptable antibody specificities.
View Article and Find Full Text PDFHLA
September 2025
Department of Laboratory Medicine, Jeonbuk National University Medical School and Hospital, Jeonju, Republic of Korea.
DRB3*03:85 is distinguished from HLA-DRB3*03:01:01:01 by a single nonsynonymous substitution at codon 122 in exon 3.
View Article and Find Full Text PDFBlood Transfus
August 2025
EFS BloodCenter of Brittany, HLA-HPA Laboratory, Rennes, France.
Background: Non-invasive fetal HPA typing is a valuable tool to identify the pregnancies at risk of fetal and neonatal alloimmune thrombocytopenia (FNAIT). Different approaches have been developed, mainly based on real-time PCR and droplet digital-PCR. Those methods have a limited ability to multiplex and require replicates due to the contamination risk.
View Article and Find Full Text PDFHLA
September 2025
Immunology Unit, Clinical Analysis Department, Albacete University Hospital Complex, Albacete, Spain.
Genomic sequences of the HLA-DQB1*06:02:01:38, -DQB1*06:02:01:39, -DQB1*06:03:01:25, -DQB1*06:03:01:27, -DQB1*06:04:01:09 and -DQB1*06:529 alleles.
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