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Updated: Apr 28, 2026

Personalized Peptide Arrays for Detection of HLA Alloantibodies in Organ Transplantation
Published on: September 6, 2017
Two novel alleles HLA-A*02:433 and HLA-A*02:434 identified in Saudi bone marrow donors using sequence-based typing
H A Fakhoury1, D Jawdat, A S Alaskar
1Department of Basic Sciences, College of Science and Health Professions, King Saud bin Abdulaziz University for Health Sciences, National Guard Health Affairs, Riyadh, Saudi Arabia.
Two novel Human Leukocyte Antigen-A (HLA-A) alleles, HLA-A*02:433 and HLA-A*02:434, were identified in Saudi bone marrow donors. These discoveries expand the known HLA-A allele repertoire, crucial for transplantation matching.
Area of Science:
- Immunogenetics
- Molecular Biology
- Human Leukocyte Antigen (HLA) System
Background:
- The Human Leukocyte Antigen (HLA) system plays a critical role in immune response and transplantation.
- Accurate HLA typing is essential for successful allogeneic bone marrow transplantation.
- The Saudi Bone Marrow Donor Registry (SBMDR) contributes to global HLA allele diversity data.
Purpose of the Study:
- To report the identification and characterization of two previously unknown HLA-A alleles.
- To contribute novel HLA-A allele sequences to the global HLA database.
- To enhance the accuracy of HLA matching for potential bone marrow donors.
Main Methods:
- Sequence-Based Typing (SBT) was employed for high-resolution HLA allele identification.
- Analysis of nucleotide sequences to pinpoint specific variations from known alleles.
- Comparison of novel sequences against existing HLA allele databases.
Main Results:
- Two novel HLA-A alleles, designated HLA-A*02:433 and HLA-A*02:434, were discovered.
- HLA-A*02:433 differs from HLA-A*02:05:01G by a single nucleotide substitution (G>A at position 449 in exon 2), resulting in an amino acid change (Gly83Ser).
- HLA-A*02:434 differs from HLA-A*02:01:01G by a single nucleotide substitution (C>A at position 245 in exon 2), resulting in an amino acid change (Phe15Thr).
Conclusions:
- The identified alleles likely arose from point mutations within existing HLA-A*02 subtypes.
- These novel alleles represent important additions to the HLA-A genetic diversity.
- Accurate identification of these alleles is vital for improving HLA matching in bone marrow registries.
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