Extracellular vesicles from serum samples of mycobacteria patients induced cell death of THP-1 monocyte and PBMC

Background Extracellular vesicles (EVs) play a key role in cell communication and the pathogenesis of some diseases. EVs may accelerate cell death during the course of mycobacterial infection and are also considered as a new vaccine design, drug delivery, and biomarker candidates. The current study evaluates the effects of EVs from serum samples of mycobacteria-infected patients on THP-1 monocytes and PBMC cells. Method EVs were purified from the serum, then cultured separately with THP-1 monocytes and PBMCs. The cell death was determined through annexin V-FITC and PI staining. GW4869, an EVs inhibitor, was used to determine if EVs released from serum could increase THP-1 monocytes cell death. Results The cell death was significantly increased in the presence of 10 mu g/ml and 5 mu g/ml concentrations of the purified EVs (p < 0.05). Minimal cell death was determined in 2.5 mu g/ml and 1.2 mu g/ml (p < 0.05). Up to 85% of the cells were viable in the presence of the GW4869 inhibitor (p < 0.05). Conclusion Direct infection of the cells with EVs released from mycobacteria-infected patients samples, the multiplicity of infection with the EVs, and virulent or avirulent mycobacteria may change the status of the cell death. The isolated EVs from serum samples of patients with mycobacterial infection accelerated cell death, which means that they might not be considered as an optimal tool for developing drug delivery and vaccine against tuberculosis.

Automated summary

This study evaluates the effects of extracellular vesicles (EVs) from serum samples of mycobacteria-infected patients on THP-1 monocytes and PBMC cells. The results show that the isolated EVs from serum samples of patients with mycobacterial infection accelerated cell death. This suggests that they might not be considered as an optimal tool for developing drug delivery and vaccine against tuberculosis.