PO.TB09.03 · 肿瘤生物学
结合新型数据分析算法利用One Lambda LABType产品检测HLA等位基因基因组缺失的可行性
Feasibility to detect genomic loss of HLA alleles by One Lambda LABType products combined with novel data analysis algorithm
作者与单位 Authors & Affiliations
摘要 Abstract
中文摘要
人类白细胞抗原(HLA)杂合性缺失是异基因造血干细胞移植治疗的髓系白血病复发中经常观察到的现象。多项实体瘤研究也描述了HLA缺失(Montesion等,2021;Zhang等,2022),其中HLA缺失对于接受HLA限制性免疫治疗的患者可能尤为重要。在复发期间识别杂合性缺失(LOH)可为受累患者的治疗选择提供关键信息。One Lambda LABType产品采用反向序列特异性寡核苷酸(rSSO)分型方法,配合LABScan 100或LABScan3D仪器,可提供多达11个HLA位点的HLA分型。尽管该产品在移植诊断实践中用于HLA基因分型,我们探索了使用LABType试剂盒检测人类基因组中HLA等位基因完全或部分缺失的潜在可行性。我们使用对全部11个HLA位点均有充分表征的纯合DNA样本,在每种混合物中测试不同的DNA比例以模拟LOH特征,并使用One Lambda LABType产品对若干位点的所有样本进行分析。我们新的HLA缺失分析算法能够清晰区分纯合DNA与仅含10%次要等位基因的DNA混合物。该检测能够清晰区分1:1的DNA混合物与含30%、20%和10%次要等位基因的混合物;比较不同SSO产品显示,LABType CWD试剂盒对残余等位基因的定量置信度更高。为进一步检验我们的算法,我们测试了3种DNA的混合物以模拟单倍体相合干细胞移植,即供者与患者共享一组HLA等位基因,而供者的另一等位基因不同。我们通过以不同比例混合代表杂合供者和两个患者等位基因的这3种DNA,模拟了不同水平的嵌合状态和不同水平的HLA缺失。实验证明LABType CWD检测能够在每次反应20 ng总DNA中检测到低至1%的次要等位基因。使用LABType技术对完全或部分HLA缺失进行新数据分析方法的进一步评估,可能对移植医学相关研究和肿瘤学领域均有益处。该新算法仅供研究使用,目前尚未商业化。
查看英文原文 English abstract
Loss of heterozygosity in human leukocyte antigens (HLA) is a phenomenon frequently observed in relapses of myeloid leukemia treated by allogeneic hematopoietic stem cell transplantation. Loss of HLA was also described in multiple studies of solid tumors (Montesion et al. 2021, Zhang et al. 2022) where loss of HLA may be particularly important for patients treated by HLA restrictive immunotherapy. Identifying loss of heterozygosity (LOH) during relapses may provide information critical for treatment selection in affected patients. One Lambda LABType products utilize reverse-sequence-specific oligonucleotide (rSSO) typing method with the LABScan 100 or LABScan3D instruments, to provide HLA typing in up to 11 HLA loci. Though this product is used for HLA genotyping in transplant diagnostic practices, we explored potential feasibility to use LABType kits to detect complete or partial loss of HLA alleles in human genome. We used homozygous DNA samples well characterized for all 11 HLA loci and tested different ratios of DNAs in each mixture to mimic LOH characteristics and analyzed all samples with One Lambda LABType products for several loci. Our new loss of HLA analysis algorithm was able to clearly distinguish between homozygous DNA and DNA mix containing only 10% of minor allele. Assay allowed clearly distinguish 1:1 DNA mix from 30, 20 and 10% of minor allele and comparing different SSO products showed that LABType CWD kits were quantifying residual allele with higher level of confidence. To challenge our algorithm further, we tested mixture of 3 DNAs imitating haplo-matched stem cell transplant, when donor is sharing one set of HLA alleles with the patient while other donor's allele is different. We mimicked different levels of chimerism and different levels of HLA loss by mixing these 3 DNAs representing heterozygous donor and two patients alleles in different ratios. Experiment demonstrated ability of LABType CWD test to detect as little as 1% of minor allele present in 20 ng of total DNA per reaction. Further evaluation of new data analysis approach using LABType technology for complete or partial loss of HLA may be beneficial for both transplant medicine related research and oncology fields. New algorithm is intended for research use only and is not commercially available at this time.
利益披露 Disclosure
S. Argounova,
Thermo Fisher Scientific Employment.
B. Valdez,
Thermo Fisher Scientific Employment.
K. Lam,
Thermo Fisher Scientific Employment.
H. Bennett,
Thermo Fisher Scientific Employment.
A. Chikova,
Thermo Fisher Scientific Employment.