Circulating mesenchymal stem cells in sulfur mustard-exposed patients with long-term pulmonary complications

被引:4
作者
Ghazanfari, Tooba [1 ,2 ]
Ghaffarpour, Sara [1 ]
Kariminia, Amina [3 ]
Salehi, Eisa [4 ]
Hashemi, Seyed Mahmoud [5 ]
Ardestani, Sussan Kaboudanian [6 ]
Moghadam, Keivan Gohari [7 ]
Mirsharif, Ensieh Sadat [1 ]
Dilmaghanian, Razieh [1 ]
Fadaei, Abbas [8 ]
Faghihzadeh, Soghrat [9 ]
机构
[1] Shahed Univ, Immunoregulat Res Ctr, Tehran, Iran
[2] Shahed Univ, Dept Immunol, 1471 North Karegar St, Tehran, Iran
[3] Univ British Columbia, Pediat Dept, British Columbia Childrens Hosp, Res Inst,Med, Vancouver, BC, Canada
[4] Univ Tehran Med Sci, Sch Med, Dept Immunol, Tehran, Iran
[5] Shahid Beheshti Univ Med, Sch Med, Dept Immunol, Sci, Tehran, Iran
[6] Univ Tehran, Inst Biochem & Biophys, Tehran, Iran
[7] Univ Tehran Med Sci, Fac Med, Internal Med Dept, Tehran, Iran
[8] Shahid Beheshti Univ Med Sci, Shahid Labbafinejad Hosp, Dept Pulmonol & Intens Care Med, Tehran, Iran
[9] Zanjan Univ Med Sci, Dept Biostat & Social Med, Zanjan, Iran
关键词
Mesenchymal stem cell; Sulfur mustard; Mustard gas; Pulmonary complications; Flow cytometry; AIRWAY EPITHELIAL-CELLS; BRONCHIOLITIS OBLITERANS; SPONTANEOUS SPUTUM; LUNG; APOPTOSIS; PROLIFERATION; MECHANISMS; CIVILIANS; CYTOKINES; TISSUE;
D O I
10.1016/j.toxlet.2019.05.015
中图分类号
R99 [毒物学(毒理学)];
学科分类号
100405 ;
摘要
Sulfur mustard (SM) is a toxic agent that causes acute and long-term pulmonary complications. Recent evidence has shown the impact of SM on mesenchymal stem cells (MSCs). These cells have a critical role in repairing the damaged tissues. In this study, we evaluated the mobilization of MSCs in SM-exposed patients with long-term pulmonary complications. Fifty-nine SM-injured patients with prolonged pulmonary complications and 20 healthy individuals were included. Patients were classified based on taking drugs, having comorbidities, and severity of respiratory consequence. MSCs with phenotype of CD45-CD44(+)CD29(+)CD105(+) were evaluated in peripheral blood using flow cytometry. Circulating MSCs were lower in SM-exposed patients compared to the control group (0.93 vs. 2.72 respectively, P = 0.005). No significant difference was observed in the MSC count between patients taking corticosteroids or antibiotics and those patients not taking them. Comorbidities like liver and kidney diseases had changed the count of MSCs in SM-exposed subjects. In addition, the frequency of MSCs did not show any association with the severity of long-term pulmonary complications. In conclusion, SM-exposure causes a decline in the frequency of circulating MSCs in survivors. The lower number of the peripheral MSC population in SM-exposed patients was not affected by taking corticosteroids or antibiotics, but comorbidities are probably involved in MSC frequency. The decreases observed in the number of circulating MSCs was not associated with the severity of the pulmonary complications; however, further studies in mustard lung models are required to demonstrate the therapeutic or pathologic role of MSCs in SM injuries.
引用
收藏
页码:188 / 194
页数:7
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