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Table 1 Research on radiation-induced lung injury treated with MSC-based therapy

From: Mesenchymal stem cell-based therapy for radiation-induced lung injury

Study

Model

Cell type

Route

Efficacy results

Wei et al. 2017 [46]

Mice

UC-MSCs transduced or not to express SOD3

iv

The early treatment with UC-MSCs alone significantly reduced radiation pulmonary fibrosis, with further improvement by administration of SOD3-infected UC-MSCs

Klein et al. 2017 [47]

Mice

BM-MSCs

iv

As a MSC-secreted factor, MSC-derived SOD1 is involved in the protective action of MSCs, and it plays a pivotal role against oxidative damage

Chen et al. 2016 [45]

Mice

Mn-SOD-MSCs

iv

Mn-SOD-MSCs were successful in modulating RILI in mice

Zhang et al. 2015 [29]

Human lung fibroblasts

UC-MSCs

Cocultured

Coculture of nHLFs with HU-MSCs weakened the radiation-induced activation of Wnt/β-catenin signaling. Wnt/β-catenin signaling became a potential therapeutic target for attenuating RILI

Xia et al. 2016 [36]

Mice

BM-MSCs

iv

Low-dose hBM-MSC therapy in a dose-dependent manner better contributed to functional recovery in mice

Jiang et al. 2015 [39]

Rats

AD-MSCs

iv

AD-MSCs could relieve RILI by reducing serum levels of IL-1, IL-6, and TNF-α, increasing levels of IL-10, and downregulating TGF-β1, α-SMA, and type 1 collagen levels in irradiated lung tissues

Wang et al. 2014 [10]

Rats

UC-MSCs

iv

The UC-MSCs had definite therapeutic effects on acute radiation injury in rats

Klein et al. 2016 [33]

Mice

BM-MSCs

iv

Therapy with BM-MSCs alleviated RILI and reduced the risk of lung metastasis

Hu et al. 2013 [43]

Mice

Trx-1-overexpressing hUC-MSCs

iv

Trx-1-overexpressing hUC-MSCs prolonged the survival of injured mice

Wang et al. 2013 [42]

Mice

AD-HGF-modified MSCs

iv

AD-HGF-modified MSCs did not reduce inflammation of the lungs but inhibited fibrosis

Xue et al. 2013 [31]

Mice

AD-sTβR-MSCs

iv

MSCs and AD-sTβR-MSCs adopted the characteristics of alveolar type II (ATII) cells and significantly alleviated lung injury

Kursova et al. 2009 [34]

Mice and humans

Autologous MSCs

iv

The increasing accumulation of transplanted stem cells in the lung tissue decreased the mortality rate of mice with RILI followed by thoracic irradiation and cell therapy with MSCs did not induce progression of the underlying oncological disease in clinical trial

  1. AD adipose tissue, BM bone marrow, h human, HGF hepatocyte growth factor, IL interleukin, iv intravenous, Mn manganese, MSC mesenchymal stem cell, nHLF normal human lung fibroblast, RILI radiation-induced lung injury, SMA smooth muscle actin, SOD superoxide dismutase, TGF transforming growth factor, TNF tumor necrosis factor, UC umbilical cord