Daggett C W, Yeatman M, Lodge A J, Chen E P, Linn S S, Gullotto C, Frank M M, Platt J L, Davis R D
Department of Surgery, Duke University Medical Center, Durham, N.C. 27710, USA.
J Thorac Cardiovasc Surg. 1998 Jan;115(1):19-27. doi: 10.1016/s0022-5223(98)70438-6.
The use of nonhuman lung donors, such as swine, has the potential to provide an unlimited supply of organs. However, hyperacute rejection has prevented pulmonary xenotransplantation.
Our aim was to test the hypothesis that immunodepletion by pretransplantation swine lung perfusion will prevent hyperacute swine-to-primate pulmonary xenograft rejection and allow for a functional swine pulmonary xenograft.
Seven baboons underwent left pneumonectomy followed by orthotopic transplantation of the swine left lung. Four baboons received immunodepletion by perfusion with swine lungs before transplantation, and three received no treatment before transplantation.
After transplantation, pulmonary xenografts from immunodepleted baboons had a low pulmonary vascular resistance and a high pulmonary blood flow compared with control animals, which had a high pulmonary vascular resistance and a low pulmonary blood flow. After 60 minutes of reperfusion, three of four immunodepleted animals also tolerated complete occlusion of the right pulmonary artery, with the baboon relying completely on the swine pulmonary xenograft for respiratory function for 11 hours. Pathologic analysis of peripheral lung biopsy specimens taken from control lungs displayed alveolar disruption and hemorrhage within small vessels, whereas swine lungs transplanted into immunodepleted baboons displayed little histologic evidence of injury. Furthermore, pulmonary xenografts transplanted into immunodepleted baboons demonstrated excellent respiratory function and adequate hemodynamics during occlusion of the right pulmonary artery.
Hyperacute pulmonary xenograft rejection can be prevented by pretransplantation swine lung perfusion. Swine pulmonary xenografts can provide complete respiratory support in primates when rejection is prevented.
使用非人类肺供体,如猪,有可能提供无限的器官供应。然而,超急性排斥反应阻碍了肺异种移植。
我们的目的是检验以下假设,即移植前猪肺灌注进行免疫清除可预防猪到灵长类动物的超急性肺异种移植排斥反应,并使猪肺异种移植具有功能。
7只狒狒接受左肺切除术,随后进行猪左肺原位移植。4只狒狒在移植前通过猪肺灌注进行免疫清除,3只在移植前未接受治疗。
移植后,与肺血管阻力高、肺血流量低的对照动物相比,免疫清除的狒狒的肺异种移植肺血管阻力低、肺血流量高。再灌注60分钟后,4只免疫清除的动物中有3只也能耐受右肺动脉完全闭塞,这只狒狒完全依靠猪肺异种移植进行呼吸功能达11小时。取自对照肺的外周肺活检标本的病理分析显示肺泡破坏和小血管内出血,而移植到免疫清除的狒狒体内的猪肺几乎没有损伤的组织学证据。此外,移植到免疫清除的狒狒体内的肺异种移植在右肺动脉闭塞期间表现出良好的呼吸功能和足够的血流动力学。
移植前猪肺灌注可预防超急性肺异种移植排斥反应。当排斥反应得到预防时,猪肺异种移植可为灵长类动物提供完全的呼吸支持。