Department of Nephrology Aristotle University of Thessaloniki, Hippokration Hospital, Thessaloniki, Greece.
Department of Immunology, National Peripheral Histocompatibility Center, Hippokration Hospital, Thessaloniki, Greece.
Front Immunol. 2022 May 9;13:841031. doi: 10.3389/fimmu.2022.841031. eCollection 2022.
End stage renal disease (ESRD) engenders detrimental effects in the Immune system, manifested as quantitative alterations of lymphocyte subpopulations, akin, albeit not identical to those observed during the ageing process. We performed dimensionality reduction of an extended lymphocyte phenotype panel of senescent and exhaustion related markers in ESRD patients and controls with Principal Component Analysis (PCA) and Uniform Manifold Approximation and Projection (UMAP). The plane defined by the first two principal components of PCA showed two fuzzy clusters, for patients and controls, respectively, with loadings of non-senescent markers pointing towards the controls' centroid. Naive lymphocytes were reduced in ESRD patients compared to controls (CD4+CD45RA+CCR7+ 200(150-328) . 426(260-585cells/μl respectively, = 0.001, CD19+IgD+CD27- 54(26-85) . 130(83-262)cells/μl respectively, < 0.001). PCA projections of the multidimensional ESRD immune phenotype suggested a more senescent phenotype in hemodialysis compared to hemodiafiltration treated patients. Lastly, clustering based on UMAP revealed three distinct patient groups, exhibiting gradual changes for naive, senescent, and exhausted lymphocyte markers. Machine learning algorithms can distinguish ESRD patients from controls, based on their immune-phenotypes and also, unveil distinct immunological groups within patients' cohort, determined possibly by dialysis prescription.
终末期肾病 (ESRD) 会对免疫系统产生有害影响,表现为淋巴细胞亚群数量的改变,类似于但不完全等同于衰老过程中观察到的改变。我们通过主成分分析 (PCA) 和一致流形逼近和投影 (UMAP) 对 ESRD 患者和对照组的衰老和衰竭相关标志物的扩展淋巴细胞表型进行了降维处理。PCA 的前两个主成分定义的平面显示了两个模糊簇,分别代表患者和对照组,非衰老标志物的负荷指向对照组的质心。与对照组相比,ESRD 患者的幼稚淋巴细胞减少(CD4+CD45RA+CCR7+ 200(150-328). 426(260-585cells/μl,分别为=0.001,CD19+IgD+CD27- 54(26-85). 130(83-262)cells/μl,分别为 < 0.001)。多维 ESRD 免疫表型的 PCA 投影表明,与血液透析滤过相比,血液透析患者的表型更衰老。最后,基于 UMAP 的聚类揭示了三个不同的患者群体,表现出幼稚、衰老和耗竭淋巴细胞标志物的逐渐变化。机器学习算法可以根据患者的免疫表型区分 ESRD 患者和对照组,还可以揭示患者队列中不同的免疫群体,这可能取决于透析方案。