Detection of 6pLOH in an aplastic anemia patient by in phase HLA genotyping.
Eri KikkawaTakashi ShiinaAtsuko ShigenariYuki OzakiShingo SuzukiKiyoshi AndoMakoto OnizukaPublished in: HLA (2020)
Recent studies have reported loss of heterozygosity in the chromosome 6p arms (6pLOH) of acquired aplastic anemia (AA) patients, and in tumor cells trying to escape the autoimmune system. We thus sought to establish detection methods for LOH to investigate the mechanisms underlying AA and tumor immunity. Herein, we report our evaluation of 6pLOH in a patient with severe AA patient using super-high resolution, single-molecule, sequence-based typing (SS-SBT). The highest ratios of 6pLOH detection were observed during the patient's treatment with granulocyte colony stimulating factor (G-CSF). This result suggested that most of the neutrophil precursor cells stimulated by G-CSF already had LOH in the HLA lesion. The SS-SBT method is a simple NGS method that provides complete HLA allele coverage.
Keyphrases
- single molecule
- case report
- high resolution
- chronic kidney disease
- end stage renal disease
- loop mediated isothermal amplification
- ejection fraction
- induced apoptosis
- real time pcr
- newly diagnosed
- gene expression
- label free
- cell death
- mass spectrometry
- dna methylation
- iron deficiency
- oxidative stress
- drug induced
- peritoneal dialysis
- signaling pathway
- prognostic factors
- atomic force microscopy
- acute myeloid leukemia
- endoplasmic reticulum stress
- copy number