Polymer science for macroencapsulation of cells for central nervous system transplantation

Frank T Gentile, Edward J Doherty, David H Rein, Molly S Shoichet, Shelley R Winn
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引用次数: 43

Abstract

The goal of encapsulated cell therapy research is to develop implants containing living xenogeneic cells to treat serious and disabling human conditions. The enabling concept is straightforward: cells or small clusters of tissue are surrounded by a selective membrane barrier which admits oxygen and required metabolites, releases bioactive cell secretions but restricts the transport of the larger cytotoxic agents of the body's immune defense system. Use of a selective membrane both eliminates the need for chronic immunosuppression in the host and allows cells to be obtained from non-human sources, thus avoiding the cell-sourcing constraints which have limited the clinical application of general successful investigative trials of unencapsulated cell transplantation for chronic pain, Parkinson's disease, and type I diabetes. Target applications for encapsulated cell therapy include these same disorders as well as other disabilities caused by loss of secretory cell function which cannot be adequately treated by current organ transplantation or drug therapies and conditions potentially capable of responding to local sustained delivery of growth factors and other biologic response modifiers. Several types of device configurations are possible. Here we focus on easily retrieved, non-vascularized, macrocapsules. Such devices have four basic components: a hollow fiber or flat sheet membrane (usually thermoplastic based), cells (primary or dividing), and extracellular matrix (natural or synthetic) to promote cell viability and function, and other device components such as seals, tethers and radio-opaque markers. Choice of membrane and extracellular matrix polymers as well as issues surrounding implantation and biocompatibility evaluation are complex, inter-related, and ultimately driven by implantation site and delivery requirements. Cross species immunoisolated cell therapy has been validated small and large animal models of chronic pain, Parkinson's disease, and type 1 diabetes and is under active investigation by several groups in animal models of Huntington's, Hemophilia, Alzheimer's, ALS, and other CNS disorders.

用于中枢神经系统移植的细胞大胶囊化的高分子科学
包膜细胞治疗研究的目标是开发含有活异种细胞的植入物来治疗严重和致残的人类疾病。这个可行的概念很简单:细胞或小簇组织被一层选择性的膜屏障所包围,它允许氧气和所需的代谢物进入,释放生物活性细胞分泌物,但限制了身体免疫防御系统中较大的细胞毒性物质的运输。选择性膜的使用既消除了对宿主慢性免疫抑制的需要,又允许从非人类来源获得细胞,从而避免了细胞来源的限制,这种限制限制了慢性疼痛、帕金森病和I型糖尿病的无包膜细胞移植临床应用的一般成功调查试验。包膜细胞治疗的目标应用包括这些相同的疾病以及其他由分泌细胞功能丧失引起的残疾,这些疾病无法通过当前的器官移植或药物治疗得到充分治疗,以及可能对局部持续递送生长因子和其他生物反应调节剂有反应的条件。有几种类型的设备配置是可能的。这里我们着重于容易回收的、非血管化的大胶囊。这种装置有四个基本组成部分:中空纤维或平板膜(通常基于热塑性塑料),细胞(原生或分裂)和细胞外基质(天然或合成),以促进细胞活力和功能,以及其他装置组件,如密封件,系绳和无线电不透明标记。膜和细胞外基质聚合物的选择以及围绕植入和生物相容性评估的问题是复杂的,相互关联的,最终由植入位置和递送要求驱动。跨物种免疫分离细胞疗法已经在慢性疼痛、帕金森氏病和1型糖尿病的小型和大型动物模型中得到验证,并且正在积极研究亨廷顿病、血友病、阿尔茨海默病、ALS和其他中枢神经系统疾病的动物模型。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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