小RNA
病毒载量
生物
移植
长非编码RNA
核糖核酸
病毒
外周血
微阵列分析技术
病毒学
计算生物学
免疫学
医学
基因
基因表达
遗传学
内科学
作者
Huadi Chen,Anli Yang,Chenglin Wu,Jun Lin,Xiaoping Wang,Mengran Peng,Dian Li,Tao Zhang,Qiang Zhao,Xiaoshun He
标识
DOI:10.1080/21691401.2021.2011304
摘要
Viral infection seriously affects the survival and life quality of transplanted patients without an accurate diagnosis during the early stage. Herein, we aimed to develop a novel diagnostic method based on non-coding RNAs expression in peripheral blood. An immunosuppressive mouse model of viral infection after transplantation was established. Differentially expressed non-coding RNAs were distinguished by microarray analyses in the virus-infected group. After homology analysis, 46 miRNAs and 24 lncRNAs were further verified by qRT-PCR in the peripheral blood samples of transplanted patients. Compared with normal transplanted patients, miR-29b, miR-185, and NR_073415.2 were significantly downregulated in the PBMC of post-transplant patients with viral infection. Based on the expression of the above three RNAs, principal component analysis (PCA) identified a slight overlap between the two groups. A 3-non-coding-RNA detection panel was constructed by the support vector machine analysis (SVM), whose loss rate was 14.71%. The area under the curve of it was 0.909. With the optimal cut-off value (Y = 0.328), the sensitivity was 0.929 and the specificity was 0.781. Therefore, based on non-coding RNAs expressions, a detection panel for viral infection after organ transplantation was formed with high diagnostic specificity and sensitivity.
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