Bose Sayantan, Do Vicki, Testini Chiara, Jadhav Suchita S, Sailliet Nicolas, Kho Alvin T, Komatsu Masaki, Boneschansker Leo, Kong Sek Won, Wedel Johannes, Briscoe David M
Transplant Research Program, Boston Children's Hospital, Boston, MA, United States.
Division of Nephrology, Boston Children's Hospital, Boston, MA, United States.
Front Transplant. 2025 Feb 4;4:1518772. doi: 10.3389/frtra.2025.1518772. eCollection 2025.
It is increasingly appreciated that the expression of immunoregulatory molecules within tumors have potential to shape a microenvironment that promotes local immunoevasion and immunoregulation. However, little is known about tissue-intrinsic immunomodulatory mechanisms following transplantation. We propose that differences in the phenotype of microvascular endothelial cells impact the alloantigenicity of the graft and its potential to promote immunoregulation following transplantation. We focus this review on the concept that graft-dependent immunoregulation may evolve post-transplantation, and that it is dependent on the phenotype of select subsets of intragraft endothelial cells. We also discuss evidence that long-term graft survival is critically dependent on adaptive interactions among immune cells and endothelial cells within the transplanted tissue microenvironment.
人们越来越认识到,肿瘤内免疫调节分子的表达有可能塑造一个促进局部免疫逃逸和免疫调节的微环境。然而,关于移植后组织内在的免疫调节机制却知之甚少。我们提出,微血管内皮细胞表型的差异会影响移植物的同种抗原性及其在移植后促进免疫调节的潜力。本综述聚焦于这样一个概念,即移植物依赖性免疫调节可能在移植后演变,并且它依赖于移植物内特定内皮细胞亚群的表型。我们还讨论了证据,即长期移植物存活严重依赖于移植组织微环境中免疫细胞和内皮细胞之间的适应性相互作用。