Soleimanpour S A, Sekiguchi D R, LaRosa D F, Luning Prak E T, Naji A, Rickels M R
Division of Endocrinology, Diabetes, and Metabolism, University of Pennsylvania School of Medicine, Philadelphia, Pennsylvania 19104, USA.
Transplant Proc. 2011 Nov;43(9):3302-6. doi: 10.1016/j.transproceed.2011.10.004.
The aim was to describe a case of hypersensitivity to rabbit antithymocyte globulin (rATG) occurring in the context of islet transplantation.
A 36-year-old woman with type 1 diabetes was admitted for islet transplantation. rATG was administered the first day (1.5 mg/kg) with methylprednisolone (2 mg/kg), and on the second day (1.5 mg/kg) without glucocorticoid to avoid potential toxicity to the anticipated islet transplant.
At the end of the rATG infusion on the second day she developed hives over her face, chest, and back and tender erythema at her intravenous site (Arthus reaction). Islet transplantation was not performed. She reported exposure to a pet rabbit for 2 years in childhood. Overnight, fever developed and the rash evolved into an erythematous morbilliform eruption affecting the torso. Serum high-sensitivity C-reactive protein (hsCRP) and the erythrocyte sedimentation rate (ESR) were elevated; serum complements C3 and C4 were normal. She received prednisone (50 mg) with subsequent resolution of the rash. Nine days after her initial reaction, she developed a recurrence of the rash and fever with arthralgias; levels of C3 and C4 had fallen. Methylprednisolone (125 mg, twice) was required for symptom improvement, and was gradually tapered as prednisone over the next 4 weeks with resolution of the complement, ESR, and hsCRP abnormalities. Five months after the initial attempt at islet transplantation, she returned to receive 7,879 IE/kg via portal vein infusion under basiliximab, etanercept, tacrolimus, and sirolimus immunosuppression and has required no to low-dose (0.1 U/kg/d) insulin to maintain near-normal glycemic control for > 12 months after transplantation.
Our patient's initial hypersensitivity reaction to rATG was followed by immune-complex type 3 hypersensitivity (serum sickness) requiring high-dose glucocorticoids. Canceling the initial islet infusion proved to be wise, and the patient subsequently did well with islet transplantation under an alternative induction agent.
描述1例在胰岛移植背景下发生的对兔抗胸腺细胞球蛋白(rATG)过敏的病例。
一名36岁1型糖尿病女性因胰岛移植入院。第一天给予rATG(1.5mg/kg)及甲泼尼龙(2mg/kg),第二天给予rATG(1.5mg/kg)且未使用糖皮质激素,以避免对预期的胰岛移植产生潜在毒性。
在第二天rATG输注结束时,她的面部、胸部和背部出现荨麻疹,静脉穿刺部位出现压痛性红斑(阿瑟斯反应)。未进行胰岛移植。她报告童年时曾接触宠物兔2年。一夜之间,出现发热,皮疹演变为影响躯干的红斑麻疹样皮疹。血清高敏C反应蛋白(hsCRP)和红细胞沉降率(ESR)升高;血清补体C3和C4正常。她接受泼尼松(50mg)治疗后皮疹消退。在她最初出现反应9天后,皮疹和发热复发并伴有关节痛;C3和C4水平下降。需要给予甲泼尼龙(125mg,2次)来改善症状,并在接下来的4周内逐渐减量为泼尼松,随着补体、ESR和hsCRP异常情况的缓解,最终停药。在首次尝试胰岛移植5个月后,她返回接受通过门静脉输注7879 IE/kg胰岛,同时使用巴利昔单抗、依那西普、他克莫司和西罗莫司进行免疫抑制,移植后12个月以上,她仅需要极低剂量(0.1 U/kg/d)胰岛素来维持血糖接近正常控制。
我们的患者最初对rATG发生过敏反应,随后出现需要高剂量糖皮质激素治疗的3型免疫复合物超敏反应(血清病)。取消最初的胰岛输注被证明是明智的,该患者随后在使用另一种诱导剂的情况下进行胰岛移植,效果良好。