Parker W, Lin S S, Platt J L
Department of Surgery, Duke University Medical Center, Durham, NC 27710, USA.
Transplantation. 2001 Jan 27;71(2):313-9. doi: 10.1097/00007890-200101270-00025.
Acute vascular rejection (AVR) is an important immunological barrier to xenotransplantation. Thought to be initiated by xenoreactive antibodies, acute vascular rejection might, in principle, be avoided by engineering animals to express low levels of antigen. The extent to which antigen expression would have to be decreased to achieve such a goal is unknown.
We estimated the decrease in expression of a xenogeneic antigen, Galalpha1-3Gal, which might be needed to avert acute vascular rejection of xenotransplants based on the decrease in antibody binding to endothelium that would prevent tissue damage.
The level of decrease needed in Galalpha1-3Gal expression needed to avoid acute vascular rejection was estimated to exceed 96% of baseline. The extent of the decrease needed reflected, in part, a substantial "excess" of Galalpha1-3Gal on porcine endothelial cell surfaces.
Although the change in antigen expression required to avoid acute vascular rejection might be conditioned by various factors, the very large magnitude of this change necessitates application of highly efficient approaches to antigen modification.
急性血管排斥反应(AVR)是异种移植的一个重要免疫障碍。急性血管排斥反应被认为是由异种反应性抗体引发的,原则上,通过改造动物使其表达低水平抗原或许可以避免这种反应。为实现这一目标,抗原表达需要降低到何种程度尚不清楚。
我们根据抗体与内皮细胞结合减少从而防止组织损伤的情况,估算了避免异种移植急性血管排斥反应可能需要降低的异种抗原——α1,3-半乳糖(Galα1-3Gal)的表达量。
为避免急性血管排斥反应,Galα1-3Gal表达所需降低的水平估计超过基线的96%。所需降低的程度部分反映出猪内皮细胞表面Galα1-3Gal存在大量“过剩”。
尽管避免急性血管排斥反应所需的抗原表达变化可能受多种因素制约,但这种变化幅度极大,因此必须采用高效的抗原修饰方法。