Kaplan David, Christian Eric, Valent Jason, Anwer Faiz, Mazzoni Sandra, Samaras Christy, Williams Louis, Nakashima Megan, Raza Shahzad, Hanna Mazen, Lazarus Hillard M, Khouri Jack
CellPrint Biotechnology, Cleveland, Ohio, USA.
Department of Pathology, Case Western Reserve University, Cleveland, Ohio, USA.
J Cell Mol Med. 2025 Sep;29(18):e70850. doi: 10.1111/jcmm.70850.
The diagnosis of AL amyloidosis is often challenging due to its systemic nature and heterogeneous clinical presentation. Current serological biomarkers for diagnosis and monitoring are not optimal. We have considered the possibility that mononuclear cell-type specific molecular expression can be used to develop blood-based biomarkers to diagnose and monitor patients with AL amyloidosis. Peripheral blood monocytes and CD4 T cells from patients with documented AL amyloidosis or myeloma without amyloidosis were assessed by enhanced flow cytometric analysis for expression levels of 20 analytes chosen for the possibility that their expression levels may lead to diagnostic assays and biomarkers. We found definitive expression level differences for brain-derived neurotrophin factor (BDNF), calmodulin, and phospho-TBK1 in CD4 T cells and for phospho-GSK3β in monocytes. Logistic regression and ROC analysis showed that BDNF in CD4 T cells and heme oxygenase 1 in monocytes significantly distinguished between patients with myeloma versus patients with AL amyloidosis (AUC = 0.75). Additionally, we discovered remarkable differences in intermolecular associations between the samples from the two patient groups, suggesting the involvement of specific pathogenetic pathways. Our results demonstrate that mononuclear cell-type specific molecular expression may be useful for developing a diagnostic assay and biomarkers for patients with AL amyloidosis.
由于AL淀粉样变性具有全身性且临床表现异质性,其诊断往往具有挑战性。目前用于诊断和监测的血清生物标志物并不理想。我们考虑了这样一种可能性,即单核细胞类型特异性分子表达可用于开发基于血液的生物标志物,以诊断和监测AL淀粉样变性患者。通过增强型流式细胞术分析,对确诊为AL淀粉样变性或无淀粉样变性的骨髓瘤患者的外周血单核细胞和CD4 T细胞进行评估,检测20种分析物的表达水平,因为它们的表达水平可能有助于开发诊断检测方法和生物标志物。我们发现,脑源性神经营养因子(BDNF)、钙调蛋白和磷酸化TBK1在CD4 T细胞中的表达水平存在显著差异,磷酸化GSK3β在单核细胞中的表达水平存在显著差异。逻辑回归和ROC分析表明,CD4 T细胞中的BDNF和单核细胞中的血红素加氧酶1能够显著区分骨髓瘤患者和AL淀粉样变性患者(AUC = 0.75)。此外,我们发现两组患者样本之间的分子间关联存在显著差异,这表明特定致病途径的参与。我们的结果表明,单核细胞类型特异性分子表达可能有助于为AL淀粉样变性患者开发诊断检测方法和生物标志物。