Citations 60

Characterisation of the Novel HLA‐DRB1*10:52 Allele by Next‐Generation Sequencing and Oxford Nanopore Sequencing

HLA | August 15, 2026 | Volume: 108 | Issue: 2 | Pages: No page available

10.1111/tan.70921 | PMID 42601336

ABSTRACT HLA‐DRB1*10:52 is characterised by a single nucleotide substitution in codon 133 in exon 3.
Characterisation of the Novel HLA‐DQA1*01:205N Allele by Next Generation Sequencing and Oxford Nanopore Sequencing

HLA | August 15, 2026 | Volume: 108 | Issue: 2 | Pages: No page available

10.1111/tan.70917 | PMID 42601337

ABSTRACT The HLA‐DQA1*01:205N allele is characterised by a nonsense mutation in codon 114 in exon 3.
Engraftment across major ABO blood group and rhesus E antigen incompatibility in the presence of persistent anti-E antibodies and late serologic findings coinciding with disease relapse

BMJ Case Reports | August 6, 2026 | Volume: 19 | Issue: 8 | Pages: e275699

10.1136/bcr-2026-275699 | PMID 42562449

ABO incompatibility is frequent in haematopoietic stem cell transplantation (HSCT), yet the clinical impact of non-ABO red blood cell (RBC) alloimmunisation remains less defined. We describe the clinical course of a man in his 50s with chronic eosinophilic leukaemia who underwent a mismatched unrelated donor (MMUD) HSCT. Despite a major ABO mismatch and high-titre pre-existing anti-E antibodies against an E-antigen positive donor, the patient achieved successful trilineage engraftment without haemolysis. Six months after the transplant, he developed severe pancytopenia and a positive direct antiglobulin test (DAT) with anti-E elution. These serologic findings coincided with disease relapse rather than isolated immune-mediated haemolysis. This case illustrates that successful engraftment is possible across RhE-incompatibility and underscores the need to interpret late serologic abnormalities within the broader context of graft function and disease status.
Genomic Confirmation of HLA‐DQA1*01:67:01 by Next Generation Sequencing and Oxford Nanopore Sequencing

HLA | July 30, 2026 | Volume: 108 | Issue: 2 | Pages: No page available

10.1111/tan.70885 | PMID 42528166

ABSTRACT HLA‐DQA1*01:67:01 is characterised by a single nucleotide substitution in codon 100 in Exon 3.
Genomic Confirmation of HLA‐DPA1*01:49 by Next Generation Sequencing and Oxford Nanopore Sequencing

HLA | July 29, 2026 | Volume: 108 | Issue: 2 | Pages: No page available

10.1111/tan.70888 | PMID 42522471

ABSTRACT HLA‐DPA1*01:49 is characterised by a single nucleotide substitution in codon 119 in exon 3.
Genomic Confirmation of HLA‐B*15:591 by Next Generation Sequencing

HLA | June 27, 2026 | Volume: 108 | Issue: 1 | Pages: No page available

10.1111/tan.70819 | PMID 42362490

ABSTRACT HLA‐B*15:591 is characterised by a single nucleotide substitution in codon 219 in exon 4.
Genomic Confirmation of HLA‐C*01:155 , by Next Generation Sequencing

HLA | June 15, 2026 | Volume: 107 | Issue: 6 | Pages: No page available

10.1111/tan.70802 | PMID 42289344

ABSTRACT HLA‐C*01:155 is characterised by a single nucleotide substitution in codon 225 in exon 4.
Characterisation of the Novel HLA‐A*26:268 Allele by Next Generation Sequencing

HLA | June 13, 2026 | Volume: 107 | Issue: 6 | Pages: No page available

10.1111/tan.70788 | PMID 42286938

ABSTRACT The novel HLA‐A*26:268 allele is characterised by a single nucleotide substitution in exon 7.
Genomic Confirmation of HLA‐DQA1*01:169 , by Next Generation Sequencing

HLA | June 11, 2026 | Volume: 107 | Issue: 6 | Pages: No page available

10.1111/tan.70794 | PMID 42272267

ABSTRACT The HLA‐DQA1*01:169 allele is characterised by a single nucleotide substitution in codon 175 in exon 3.
Blood bags under scrutiny: The dark spot investigation

Transfusion | June 10, 2026 | Volume: 66 | Issue: 8 | Pages: 1473-1474

10.1111/trf.70293 | PMID 42267681