Schuster Family Transplantation Research Center, Renal Division, Brigham and Women's Hospital, Harvard Medical School, Boston, MA 02115, USA.
Center for Transplantation Sciences, Department of Surgery, Massachusetts General Hospital, Harvard Medical School, Boston, MA 02129, USA.
Cell Rep Med. 2022 Mar 15;3(3):100559. doi: 10.1016/j.xcrm.2022.100559.
Limb transplantation is a life-changing procedure for amputees. However, limb recipients have a 6-fold greater rejection rate than solid organ transplant recipients, related in part to greater immunogenicity of the skin. Here, we report a detailed immunological and molecular characterization of individuals who underwent bilateral limb transplantation at our institution. Circulating Th17 cells are increased in limb transplant recipients over time. Molecular characterization of 770 genes in skin biopsies reveals upregulation of T cell effector immune molecules and chemokines, particularly CCL18. Skin antigen-presenting cells primarily express the chemokine CCL18, which binds to the CCR8 receptor. CCL18 treatment recruits more allo-T cells to the skin xenograft in a humanized skin transplantation model, leading to signs of accelerated graft rejection. Blockade of CCR8 remarkedly decreases CCL18-induced allo-T cell infiltration. Our results suggest that targeting the CCL18:CCR8 pathway could be a promising immunosuppressive approach in transplantation.
肢体移植是截肢患者改变生活的一种手术。然而,肢体接受者的排斥率比实体器官接受者高 6 倍,部分原因是皮肤的免疫原性更强。在这里,我们报告了在我们机构接受双侧肢体移植的个体的详细免疫和分子特征。随着时间的推移,肢体移植接受者的循环 Th17 细胞增加。对皮肤活检的 770 个基因进行分子特征分析表明,T 细胞效应免疫分子和趋化因子上调,特别是 CCL18。皮肤抗原呈递细胞主要表达趋化因子 CCL18,它与 CCR8 受体结合。CCL18 处理在人源化皮肤移植模型中募集更多同种异体 T 细胞到皮肤异种移植物,导致移植物排斥的迹象加速。CCR8 的阻断显著减少了 CCL18 诱导的同种异体 T 细胞浸润。我们的研究结果表明,靶向 CCL18:CCR8 途径可能是移植中一种有前途的免疫抑制方法。