Kim Jun-Seop, Lee Jong-Hak, Kwon Owen, Cho Jang-Hee, Choi Ji-Young, Park Sun-Hee, Kim Chan-Duck, Kim Yong-Jin, Kim Yong-Lim
Department of Internal Medicine, Kyungpook National University School of Medicine, Daegu, Korea.
Department of Internal Medicine, Daegu Fatima Hospital, Daegu, Korea.
Kidney Res Clin Pract. 2017 Jun;36(2):200-204. doi: 10.23876/j.krcp.2017.36.2.200. Epub 2017 Jun 30.
Administration of autologous mesenchymal stem cells (MSCs) has been shown to improve renal function and histological findings in acute kidney injury (AKI) models. However, its effects in chronic kidney disease (CKD) are unclear, particularly in the clinical setting. Here, we report our experience with a CKD patient who was treated by intravenous infusion of autologous MSCs derived from adipose tissue in an unknown clinic outside of Korea. The renal function of the patient had been stable for several years before MSC administration. One week after the autologous MSC infusion, the preexisting renal insufficiency was rapidly aggravated without any other evidence of AKI. Hemodialysis was started 3 months after MSC administration. Renal biopsy findings at dialysis showed severe interstitial fibrosis and inflammatory cell infiltration, with a few cells expressing CD34 and CD117, 2 surface markers of stem cells. This case highlights the potential nephrotoxicity of autologous MSC therapy in CKD patients.
自体间充质干细胞(MSC)的应用已被证明可改善急性肾损伤(AKI)模型中的肾功能和组织学表现。然而,其在慢性肾脏病(CKD)中的作用尚不清楚,尤其是在临床环境中。在此,我们报告一名CKD患者的治疗经历,该患者在韩国境外一家不知名诊所接受了静脉输注自体脂肪组织来源的MSC治疗。在MSC治疗前,患者的肾功能已经稳定了数年。自体MSC输注一周后,先前存在的肾功能不全迅速加重,且无任何其他AKI证据。MSC治疗3个月后开始血液透析。透析时的肾活检结果显示严重的间质纤维化和炎症细胞浸润,有少数细胞表达CD34和CD117,这是干细胞的两种表面标志物。该病例突出了自体MSC治疗对CKD患者潜在的肾毒性。