van den Hoogen Patricia, Huibers Manon M H, Sluijter Joost P G, de Weger Roel A
Department of Cardiology, Experimental Cardiology laboratory, University Medical Centre Utrecht, Utrecht, The Netherlands.
J Cardiovasc Transl Res. 2015 Mar;8(2):106-16. doi: 10.1007/s12265-015-9612-x. Epub 2015 Feb 5.
Cardiac allograft vasculopathy (CAV) is one of the main causes of late-stage heart failure after heart transplantation. CAV is characterized by concentric luminal narrowing of the coronary arteries, but the exact pathogenesis of CAV is still not unraveled. Many researchers show evidence of an allogeneic immune response of the recipient, whereas others show contrasting results in which donor-derived cells induce an immune response against the graft. In addition, fibrosis of the neo-intima can be induced by recipient-derived circulating cells or donor-derived cells. In this review, both donor and recipient sides of the story are described to obtain better insight in the pathogenesis of CAV. Dual outcomes were found regarding the contribution of donor and recipient cells in the initiation of the immune response and the development of fibrosis during CAV. Future research could focus more on the potential synergistic interaction of donor and recipient cells leading to CAV.
心脏移植血管病变(CAV)是心脏移植术后晚期心力衰竭的主要原因之一。CAV的特征是冠状动脉管腔同心性狭窄,但CAV的确切发病机制仍未阐明。许多研究人员证明了受体的同种异体免疫反应,而另一些人则得出了相反的结果,即供体来源的细胞会引发针对移植物的免疫反应。此外,新生内膜的纤维化可由受体来源的循环细胞或供体来源的细胞诱导。在这篇综述中,将描述故事的供体和受体两个方面,以便更好地了解CAV的发病机制。在CAV期间免疫反应的启动和纤维化的发展过程中,关于供体细胞和受体细胞的作用发现了双重结果。未来的研究可以更多地关注导致CAV的供体细胞和受体细胞之间潜在的协同相互作用。