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Ability to Regulate Immunity of Mesenchymal Stem Cells in the Treatment of Traumatic Brain Injury

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Journal Neurol Sci
Specialty Neurology
Date 2021 Aug 10
PMID 34374864
Citations 4
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Abstract

Traumatic brain injury (TBI) is characterized by broad clinical symptoms in brain insult by external damages to the skull. TBI potentially leads to severe physical, cognitive, and emotional impairment. The complex biochemical reactions of inflammatory processes in TBI significantly influence brain function and clinical sequelae's overall severity. Mesenchymal stem cell therapy has become a promising therapeutic field of treatment for serious injuries due to its ability to regulate the inflammatory microenvironment. In this study, we aimed to investigate MSC's anti-inflammatory ability through regulating leukocyte, neutrophils, and inflammatory factors (IL-6, CRP, and TNF-a), thereby reducing the trauma in the TBI. Biological effects of autologous MNC and MSC cell transplantation have been studied in 40 patients with molded TBI, after being filtered according to appropriate criteria. All patients initially received MNCs and subsequently MSCs (both intravenously) followed by continuous monitoring during treatment (2 months) with clinical cognitive indicators. The results after transplantation MSC indicated that the majority of patients experienced improved health function in different degrees during the follow-up period. Lower serum levels of inflammatory factors, leukocytes, and neutrophils population were detected following the transplantation compared with the levels prior to treatment and with the control patients. No severe symptoms were observed in patients after transplantation, despite 3-4 death cases in each group. Overall, the present study suggests that transplantation of MSC possibly regulates inflammatory factors and appears to be safe in TBI treatment.

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References
1.
Liao Y, Liu P, Guo F, Zhang Z, Zhang Z . Oxidative burst of circulating neutrophils following traumatic brain injury in human. PLoS One. 2013; 8(7):e68963. PMC: 3722225. DOI: 10.1371/journal.pone.0068963. View

2.
Reis C, Gospodarev V, Reis H, Wilkinson M, Gaio J, Araujo C . Traumatic Brain Injury and Stem Cell: Pathophysiology and Update on Recent Treatment Modalities. Stem Cells Int. 2017; 2017:6392592. PMC: 5568618. DOI: 10.1155/2017/6392592. View

3.
Daglas M, Draxler D, Ho H, McCutcheon F, Galle A, Au A . Activated CD8 T Cells Cause Long-Term Neurological Impairment after Traumatic Brain Injury in Mice. Cell Rep. 2019; 29(5):1178-1191.e6. DOI: 10.1016/j.celrep.2019.09.046. View

4.
Harting M, Jimenez F, Xue H, Fischer U, Baumgartner J, Dash P . Intravenous mesenchymal stem cell therapy for traumatic brain injury. J Neurosurg. 2009; 110(6):1189-97. PMC: 2889620. DOI: 10.3171/2008.9.JNS08158. View

5.
Huang P, Freeman W, Edenfield B, Brott T, Meschia J, Zubair A . Safety and Efficacy of Intraventricular Delivery of Bone Marrow-Derived Mesenchymal Stem Cells in Hemorrhagic Stroke Model. Sci Rep. 2019; 9(1):5674. PMC: 6450980. DOI: 10.1038/s41598-019-42182-1. View