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首页> 外文期刊>Expert review of respiratory medicine >Lung tissue bioengineering for chronic obstructive pulmonary disease: overcoming the need for lung transplantation from human donors
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Lung tissue bioengineering for chronic obstructive pulmonary disease: overcoming the need for lung transplantation from human donors

机译:用于慢性阻塞性肺病的肺组织生物工程:克服人类供体肺移植的需要

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摘要

Introduction: Chronic obstructive pulmonary disease (COPD) affects more than 380 million people, causing more than 3 million deaths annually worldwide. Despite this enormous burden, currently available therapies are largely limited to symptom control. Lung transplant is considered for end-stage disease but is severely limited by the availability of human organs. Furthermore, the pre-transplant course is a complex orchestration of locating and harvesting suitable lungs, and the post-transplant course is complicated by rejection and infection. Lung tissue bioengineering has the potential to relieve the organ shortage and improve the post-transplant course by generating patient-specific lungs for transplant. Additionally, emerging progenitor cell therapies may facilitate in vivo regeneration of pulmonary tissue, obviating the need for transplant. Areas Covered: We review several lung tissue bioengineering approaches including the recellularization of decellularized scaffolds, 3D bioprinting, genetically-engineered xenotransplantation, blastocyst complementation, and direct therapy with progenitor cells. Articles were identified by searching relevant terms (see Key Words) in the PubMed database and selected for inclusion based on novelty and uniqueness of their approach. Expert Opinion: Lung tissue bioengineering research is in the early stages. Of the methods reviewed, only direct cell therapy has been investigated in humans. We anticipate a minimum of 5-10 years before human therapy will be feasible.
机译:介绍:慢性阻塞性肺病(COPD)影响超过3.8亿人,每年在全球范围内造成300多万人死亡。尽管这种巨大的负担,目前可用的疗法主要限于症状控制。肺移植被认为是终级疾病,但受人体器官的可用性严重限制。此外,预移植过程是定位和收获合适的肺的复合核,后移植后课程通过排斥和感染复杂。肺组织生物工程有可能通过产生患者特异性肺进行移植来缓解器官短缺和改善移植后疗程。另外,出现的祖细胞疗法可以促进肺组织的体内再生,避免了移植的需要。所涵盖的地区:我们审查了几种肺组织生物工程方法,包括脱细胞的支架,3D生物印刷,转基因异种持续,胚泡互补和与祖细胞的直接治疗。通过在PubMed数据库中搜索相关条款(请参阅关键词)并根据其方法的新颖性和唯一性选择来识别文章。专家意见:肺组织生物工程研究处于早期阶段。在审查的方法中,只有在人类中才能研究直接细胞疗法。我们预期在人类治疗之前至少5-10年将是可行的。

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