Trivedi Hargovind L, Thakkar Umang G, Vanikar Aruna V, Dave Shruti D
Department of Nephrology and Transplantation Medicine, G R Doshi and K M Mehta Institute of Kidney Diseases and Research Centre (IKDRC)-Dr H L Trivedi Institute of Transplantation Sciences (ITS), Ahmedabad, Gujarat, India.
BMJ Case Rep. 2011 Sep 4;2011:bcr0720114436. doi: 10.1136/bcr.07.2011.4436.
The authors report a 17-year-female and a 19-year-male with uncontrolled insulin-dependent diabetes mellitus (IDDM) for ≥10 years, treated with insulin-secreting human adipose tissue derived mesenchymal stem cells (IS-h-ADMSC). Both had hypothyroidism and were diagnosed as polyglandular autoimmune syndrome type-3 (PGAS-3). PGAS are rare polyendocrinopathies with ≥2 endocrine disorders mediated by autoimmune mechanisms leading to hypo-function and organ failure. Therapeutic options are hormone replacement, immunosuppression and avoiding infection. The authors administered autologous H-AD-IS-MSC+bone marrow-derived haematopoietic stem cells (HSC) into portal circulation with conditioning of cyclophosphamide, bortezomib, rituximab and rabbit-antithymoglobulin. Over follow-up of 38 and 16 months, respectively, both are doing well with sustained fall of glycosylated haemoglobin (Hb1Ac) from 8.1 to 6.4% and 14.2 to 8.6%, respectively and C-peptide raised from 0.01 to 0.23 ng/ml and 0.1 to 0.34 ng/ml, respectively with sustained 40% decreased insulin requirement. Thus long-term control of IDDM in PGAS-3 with co-transplantation of H-AD-IS-MSC+HSC can be achieved safely and effectively.
作者报告了一名17岁女性和一名19岁男性,他们患有胰岛素依赖型糖尿病(IDDM)且病情控制不佳达10年以上,接受了分泌胰岛素的人脂肪组织来源间充质干细胞(IS-h-ADMSC)治疗。两人均患有甲状腺功能减退症,被诊断为3型多腺体自身免疫综合征(PGAS-3)。PGAS是罕见的多内分泌腺病,由自身免疫机制介导的≥2种内分泌疾病导致功能减退和器官衰竭。治疗选择包括激素替代、免疫抑制和避免感染。作者将自体H-AD-IS-MSC+骨髓来源的造血干细胞(HSC)经环磷酰胺、硼替佐米、利妥昔单抗和兔抗胸腺细胞球蛋白预处理后注入门静脉循环。在分别为期38个月和16个月的随访中,两人情况良好,糖化血红蛋白(Hb1Ac)分别从8.1%持续降至6.4%和从14.2%降至8.6%,C肽分别从0.01 ng/ml升至0.23 ng/ml和从0.1 ng/ml升至0.34 ng/ml,胰岛素需求量持续减少40%。因此,通过H-AD-IS-MSC+HSC联合移植可安全有效地实现PGAS-3中IDDM的长期控制。