HLA-C*14:171, a New Allele With a Rare Extracellular α3 Domain
Mirzokhid Rakhmanov1, Martin Bernheiden1, Murielle Verboom2
1Institute for Transfusion Medicine and Gene Therapy, Medical Center - University of Freiburg, Medical Faculty - University of Freiburg, University of Freiburg, Freiburg, Germany.
A novel Human Leukocyte Antigen C allele, HLA-C*14:171, has been identified. It differs from the known HLA-C*14:02:01:01 allele by a single nucleotide substitution.
Area of Science:
- Immunogenetics
- Molecular Biology
- Human Leukocyte Antigen (HLA) research
Background:
- The Human Leukocyte Antigen (HLA) system plays a critical role in immune response and transplantation.
- The HLA-C locus is a highly polymorphic region within the HLA system.
- Accurate HLA typing is essential for matching donors and recipients in organ and stem cell transplantation.
Purpose of the Study:
- To report the identification and characterization of a novel HLA-C allele.
- To describe the specific genetic variation distinguishing this new allele from a known one.
Main Methods:
- High-resolution HLA typing methodologies were employed.
- Sequence analysis was performed to identify nucleotide differences.
- Comparison of the novel sequence against existing HLA allele databases.
Main Results:
- A new HLA-C allele, designated HLA-C*14:171, was discovered.
- This allele differs from HLA-C*14:02:01:01 by a single nucleotide substitution.
- The substitution is located in codon 211 within exon 4 of the HLA-C gene.
Conclusions:
- The identification of HLA-C*14:171 expands the known HLA-C allele repertoire.
- This finding underscores the importance of continuous high-resolution HLA typing for comprehensive population genetic studies.
- Understanding such variations is crucial for improving HLA matching in clinical transplantation settings.
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