David Geffen School of Medicine at UCLA, Los Angeles, CA, USA.
Division of Gastroenterology, Hepatology and Nutrition, Department of Pediatrics, David Geffen School of Medicine at UCLA, Los Angeles, CA, USA.
Clin Transplant. 2021 Jul;35(7):e14378. doi: 10.1111/ctr.14378. Epub 2021 Jun 13.
Monitoring of intestinal allograft function remains a challenge. While frequent endoscopies and biopsies are the gold standard, no single biomarker exists to screen for intestinal transplant rejection. The novel REG3α, an antimicrobial peptide secreted by intestinal enterocytes and Paneth cells, has been associated with inflammatory bowel disease as well as intestinal graft versus host disease. Our aim was to identify and describe a role of REG3α in monitoring or predicting acute allograft rejection after intestinal transplantation (ITx). Since 2019, we have incorporated REG3α into the standard monitoring of patients after ITx. We conducted a retrospective analysis of a prospectively maintained IRB-approved database and present, herein, the results of 2 adults with irreversible intestinal failure who underwent isolated ITx under this monitoring protocol. Increases in REG3α corresponded with acute allograft rejection in both cases and preceded acute allograft rejection by 1 week in one of the cases. We describe REG3α as a non-invasive marker of acute allograft rejection after adult isolated ITx which not only corresponded with acute allograft rejection but also preceded histopathological changes by 1 week.
监测肠道移植物功能仍然是一个挑战。虽然频繁的内镜检查和活检是金标准,但目前还没有单一的生物标志物可用于筛查肠移植排斥反应。新型 REG3α 是一种由肠道肠上皮细胞和潘氏细胞分泌的抗菌肽,与炎症性肠病以及肠道移植物抗宿主病有关。我们的目的是确定并描述 REG3α 在监测或预测肠移植(ITx)后急性移植物排斥反应中的作用。自 2019 年以来,我们已将 REG3α 纳入 ITx 后患者的标准监测中。我们对一个经过前瞻性维护的、经机构审查委员会批准的数据库进行了回顾性分析,并在此介绍了根据该监测方案接受孤立性 ITx 的 2 例不可逆性肠衰竭成人患者的结果。在这两种情况下,REG3α 的增加与急性移植物排斥反应相对应,在其中 1 例中,REG3α 的增加比急性移植物排斥反应早 1 周。我们将 REG3α 描述为成人孤立性 ITx 后急性移植物排斥反应的一种非侵入性标志物,它不仅与急性移植物排斥反应相对应,而且比组织病理学变化早 1 周。