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The effect of adoptive transferring myeloid-derived suppressor cells in ventilator-induced lung injury mice.
Shan, Fangzhen; Tang, Fenglian; Liu, Yuan; Han, Xiao; Wu, Wei; Tang, Yanhua; Zhan, Qingyuan; Zhang, Nannan.
Afiliação
  • Shan F; Department of Pulmonary and Critical Care Medicine, Affiliated Hospital of Jining Medical University, Shandong, China.
  • Tang F; Medical Research Center, Affiliated Hospital of Jining Medical University, Shandong, China.
  • Liu Y; Department of Pulmonary and Critical Care Medicine, Affiliated Hospital of Jining Medical University, Shandong, China.
  • Han X; Department of Intensive care unit III, Affiliated Hospital of Jining Medical University, Shandong, China.
  • Wu W; Department of Pulmonary and Critical Care Medicine, Affiliated Hospital of Jining Medical University, Shandong, China.
  • Tang Y; Department of Pulmonary and Critical Care Medicine, Affiliated Hospital of Jining Medical University, Shandong, China.
  • Zhan Q; Department of Pulmonary and Critical Care Medicine, Affiliated Hospital of Jining Medical University, Shandong, China.
  • Zhang N; Department of Pulmonary and Critical Care Medicine, China-Japan Friendship Hospital, Beijing, China.
Heliyon ; 10(3): e25595, 2024 Feb 15.
Article em En | MEDLINE | ID: mdl-38356581
ABSTRACT
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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Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Idioma: En Revista: Heliyon Ano de publicação: 2024 Tipo de documento: Article País de afiliação: China

Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Idioma: En Revista: Heliyon Ano de publicação: 2024 Tipo de documento: Article País de afiliação: China
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