Kuo Elbert, Bharat Ankit, Dharmarajan Sekhar, Fernandez Felix, Patterson G Alec, Mohanakumar T
Department of Surgery and Pathology, Division of Cardiothoracic Surgery, Washington University School of Medicine, St. Louis, MO 63110, USA.
Immunol Res. 2005;33(1):69-81. doi: 10.1385/IR:33:1:069.
Lung transplantation is the only viable treatment option that can improve survival and enhance the quality of life of patients with end-stage lung diseases such as emphysema, cystic fibrosis, idiopathic pulmonary fibrosis, and primary pulmonary hypertension. However, the long-term survival of lung allografts is still limited by the development of bronchiolitis obliterans syndrome (BOS), an irreversible condition unresponsive to therapy. BOS is the most significant cause of long-term morbidity and mortality after lung transplantation. Over the past decade, several animal models have been developed to investigate BOS. These are valuable to elucidate the immunologic and pathologic mechanisms that lead to BOS and to test treatment options for BOS. In this review, we discuss the advantages and disadvantages of different animal models and highlight work that has been done with each model.
肺移植是唯一可行的治疗选择,能够提高诸如肺气肿、囊性纤维化、特发性肺纤维化和原发性肺动脉高压等终末期肺病患者的生存率并改善其生活质量。然而,肺同种异体移植物的长期存活仍受闭塞性细支气管炎综合征(BOS)的限制,这是一种不可逆的病症,对治疗无反应。BOS是肺移植后长期发病和死亡的最重要原因。在过去十年中,已开发出几种动物模型来研究BOS。这些模型对于阐明导致BOS的免疫和病理机制以及测试BOS的治疗方案很有价值。在本综述中,我们讨论了不同动物模型的优缺点,并重点介绍了每种模型所做的工作。