Application of peripheral blood mononuclear cells hsa-miR-8774-3p as marker of active tuberculosis
A technology for active pulmonary tuberculosis and nuclear cells, applied in the field of biomarkers, can solve the problems of long time-consuming sputum culture, difficult screening, and easy missed detection
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Embodiment 1
[0031]The application of hsa-miR-874-3p in peripheral blood mononuclear cells as a marker of active pulmonary tuberculosis. The cell line THP-1 was significantly upregulated, and the upregulated hsa-miR-874-3p may act on ATG16L1mRNA in mononuclear macrophages to regulate macrophage autophagy and participate in the infection process of Mtb. The up-regulated hsa-miR-874 has certain significance for the early diagnosis of APTB patients. Therefore, detecting the expression of hsa-miR-874 in APTB patients by qRT-PCR method can be used to diagnose the disease.
Embodiment 2
[0033] The application of hsa-miR-874-3p in peripheral blood mononuclear cells in the preparation of active tuberculosis markers, the applicant first studied hsa-miR-874-3p expression levels in PBMCs of HC and APTB patients 874-3p as a potential biomarker for the early diagnosis of APTB, and found that hsa-miR-874-3p was significantly upregulated in PBMC from APTB patients and the human mononuclear macrophage cell line THP-1 infected with Mycobacterium tuberculosis.
Embodiment 3
[0035] The application of peripheral blood mononuclear cells hsa-miR-874-3p in the preparation of active pulmonary tuberculosis diagnostic reagents, the applicant evaluated the possible interaction between hsa-miR-874-3p and the target ATG16L1 of this miRNA, and proved that hsa -miR-874-3p can participate in the regulation of tuberculosis infection by regulating macrophage autophagy.
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