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10.1016/j.heliyon.2024.e25595

http://scihub22266oqcxt.onion/10.1016/j.heliyon.2024.e25595
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suck abstract from ncbi

pmid38356581      Heliyon 2024 ; 10 (3): e25595
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  • The effect of adoptive transferring myeloid-derived suppressor cells in ventilator-induced lung injury mice #MMPMID38356581
  • Shan F; Tang F; Liu Y; Han X; Wu W; Tang Y; Zhan Q; Zhang N
  • Heliyon 2024[Feb]; 10 (3): e25595 PMID38356581show ga
  • The effects of adoptive transferring myeloid-derived suppressor cells (MDSCs) to mice with ventilator-induced lung injury (VILI) are unclear. Our objective was to investigate the effects of adoptively transferring MDSCs in VILI. The mouse model was created by introducing mechanical ventilation through a high tidal volume of 20 ml/kg for 4 h. Inflammation-induced MDSCs (iMDSCs) were collected from the bone marrow of mice with cecal ligation and puncture. iMDSCs were administrated through retrobulbar angular vein 1 h before the mechanical ventilation. The control group was anesthetized and maintained spontaneous respiration. After the termination of mechanical ventilation, bronchoalveolar lavage fluid (BALF) and lung samples 6 h were collected. The concentrations of BALF protein, levels of inflammatory mediators, and white blood cells were all significantly decreased in mice treated with iMDSCs. Histological examinations indicated reduced lung damage after iMDSCs treatment. Moreover, adoptive transfer of iMDSCs could reduce CD4(+) T-cell counts and inhibit its inflammatory cytokine secretion. iMDSCs treatment was found to had no immunostimulatory effects or cause secondary infections in mice. In conclusion, MDSCs might be a potential targeted therapy for alleviating the inflammatory response of VILI mice in a T-cell dependent manner.
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