A scoping review of trials for cell-based therapies in human spinal cord injury

被引:25
|
作者
Willison, Alice G. [1 ]
Smith, Sam [2 ]
Davies, Benjamin M. [3 ]
Kotter, Mark R. N. [3 ,4 ]
Barnett, Susan C. [5 ]
机构
[1] Newcastle Upon Tyne Univ Hosp, Northern Fdn Sch, Newcastle Upon Tyne, Tyne & Wear, England
[2] Univ Cambridge, Sch Clin Med, Cambridge, England
[3] Univ Cambridge, Dept Clin Neurosurg, Acad Neurosurg Unit, Cambridge, England
[4] Univ Cambridge, WT MRC Cambridge Stem Cell Inst, Anne McLaren Lab, Cambridge, England
[5] Univ Glasgow, Inst Infect Immun & Inflammat, Coll Med Vet & Life Sci, Glasgow, Lanark, Scotland
基金
英国惠康基金;
关键词
COLONY-STIMULATING FACTOR; MESENCHYMAL STEM-CELLS; BONE-MARROW; FUNCTIONAL RECOVERY; SCHWANN-CELLS; STROMAL CELLS; TRANSPLANTATION; REGENERATION; IMPROVEMENT; EXPRESSION;
D O I
10.1038/s41393-020-0455-1
中图分类号
R74 [神经病学与精神病学];
学科分类号
摘要
Introduction Spinal cord injury (SCI) is associated with significant and life-long disability. Yet, despite decades of research, no regenerative treatment has reached clinical practice. Cell-based therapies are one possible regenerative strategy beginning to transfer to human trials from a more extensive pre-clinical basis. Methods We therefore conducted a scoping review to synthesise all cell-based trials in SCI to consider the current state of the field and the cell transplant type or strategy with greatest promise. A search strategy of MEDLINE returned 1513 results. All clinical trials including adult human patients with acute or chronic, compete or incomplete SCI and a recorded ASIA score were sought. Exclusion criteria included non-traumatic SCI, paediatric patients and animal studies. A total of 43 studies, treating 1061 patients, were identified. Most trials evaluated cells from the bone marrow (22 papers, 660 patients) or the olfactory bulb (10 papers, 245 patients). Results Cell transplantation does appear to be safe, with no serious adverse effects being reported in the short-term. 86% of trials described efficacy as a primary outcome. However, varying degrees of outcome reporting prevented meta-analysis. No emerging cell type or technique was identified. The majority of trials, 53%, took place in developing countries, which may suggest more stringent regulatory requirements within Western countries. Conclusion We believe cell-based transplantation translation remains in its infancy and that, although further robust clinical research is required, it is an important strategy to consider in the treatment of SCI.
引用
收藏
页码:844 / 856
页数:13
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