Autologous Cell Seeding in Tracheal Tissue Engineering

被引:28
|
作者
Maughan E.F. [1 ,2 ]
Hynds R.E. [1 ]
Proctor T.J. [3 ]
Janes S.M. [1 ]
Elliott M. [4 ]
Birchall M.A. [5 ]
Lowdell M.W. [3 ]
De Coppi P. [2 ,5 ]
机构
[1] Lungs for Living Research Centre, UCL Respiratory, University College London, London
[2] Stem Cell and Regenerative Medicine Section, UCL Institute of Child Health and Great Ormond Street Hospital, 30 Guilford Street, London
[3] Centre for Cell, Gene and Tissue Therapies, Royal Free Hospital & University College London, London
[4] Great Ormond Street Hospital, London
[5] UCL Centre for Regenerative Medicine, University College London, London
基金
英国惠康基金; 英国医学研究理事会;
关键词
Autologous cell seeding; Clinical translation; Pre-clinical models; Tissue engineering; Trachea;
D O I
10.1007/s40778-017-0108-2
中图分类号
学科分类号
摘要
Purpose of Review: There is no consensus on the best technology to be employed for tracheal replacement. One particularly promising approach is based upon tissue engineering and involves applying autologous cells to transplantable scaffolds. Here, we present the reported pre-clinical and clinical data exploring the various options for achieving such seeding. Recent Findings: Various cell combinations, delivery strategies, and outcome measures are described. Mesenchymal stem cells (MSCs) are the most widely employed cell type in tracheal bioengineering. Airway epithelial cell luminal seeding is also widely employed, alone or in combination with other cell types. Combinations have thus far shown the greatest promise. Chondrocytes may improve mechanical outcomes in pre-clinical models, but have not been clinically tested. Rapid or pre-vascularization of scaffolds is an important consideration. Overall, there are few published objective measures of post-seeding cell viability, survival, or overall efficacy. Summary: There is no clear consensus on the optimal cell-scaffold combination and mechanisms for seeding. Systematic in vivo work is required to assess differences between tracheal grafts seeded with combinations of clinically deliverable cell types using objective outcome measures, including those for functionality and host immune response. © 2017, The Author(s).
引用
收藏
页码:279 / 289
页数:10
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