A safety study on intrathecal delivery of autologous mesenchymal stromal cells in rabbits directly supporting Phase I human trials

被引:28
作者
Chen, Bingkun K. [1 ]
Staff, Nathan P. [1 ]
Knight, Andrew M. [1 ]
Nesbitt, Jarred J. [1 ]
Butler, Greg W. [2 ]
Padley, Douglas J. [2 ]
Parisi, Joseph E. [3 ]
Dietz, Allan B. [2 ]
Windebank, Anthony J. [1 ]
机构
[1] Mayo Clin, Dept Neurol, Rochester, MN 55905 USA
[2] Mayo Clin, Human Cell Therapy Lab, Rochester, MN 55905 USA
[3] Mayo Clin, Dept Lab Med & Pathol, Rochester, MN 55905 USA
基金
美国国家卫生研究院;
关键词
INJURED SPINAL-CORD; EXPERIMENTAL AUTOIMMUNE ENCEPHALOMYELITIS; AMYOTROPHIC-LATERAL-SCLEROSIS; STEM-CELLS; BONE-MARROW; CEREBROSPINAL-FLUID; FUNCTIONAL RECOVERY; IMMUNE-RESPONSE; MOUSE MODEL; T-CELLS;
D O I
10.1111/trf.12938
中图分类号
R5 [内科学];
学科分类号
100201 [内科学];
摘要
BackgroundThere are no effective treatments that slow the progression of neurodegenerative diseases. A major challenge of treatment in neurodegenerative diseases is appropriate delivery of pharmaceuticals into the cerebrospinal fluid (CSF) of affected individuals. Mesenchymal stromal cells (MSCseither naive or modified) are a promising therapy in neurodegenerative diseases and may be delivered directly into the CSF where they can reside for months. In this preclinical study, we evaluated the safety of intrathecal autologous MSCs in a rabbit model. Study Design and MethodsAutologous adipose-derived MSCs (or artificial CSF) were delivered intrathecally, either with single or with repeated injections into the foramen magnum of healthy rabbits and monitored for 4 and 12 weeks, respectively. ResultsRabbits tolerated injections well and no definitive MSC-related side effects were observed apart from three rabbits that had delayed death secondary to traumatic foramen magnum puncture. Functional assessments and body weights were equivalent between groups. Gross pathology and histology did not reveal any abnormalities or tumor growth. Complete blood count data were normal and there were no differences in CSF interleukin-6 levels in all groups tested. ConclusionOur data suggest that intrathecal delivery of autologous MSCs is safe in a rabbit model. Data from this study have supported two successful investigational new drug applications to the Food and Drug Administration, resulting in the initiation of two clinical trials using autologous MSCs in amyotrophic lateral sclerosis and multiple system atrophy.
引用
收藏
页码:1013 / 1020
页数:8
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