Nga Hong Si, Garcia Paula Dalsoglio, Contti Mariana Moraes, Takase Henrique Mochida, de Carvalho Maria Fernanda Cordeiro, de Andrade Luis Gustavo Modelli
Universidade Estadual Paulista, Brazil.
J Bras Nefrol. 2015 Apr-Jun;37(2):206-11. doi: 10.5935/0101-2800.20150033.
Indications for induction therapy is not consensual in living donors.
The objective of this study was compare no induction with thymoglobulin and basiliximab induction in the incidence of acute rejection in kidney transplantation with living donor.
We select all cases of renal transplantation with living donor performed in Hospital das Clínicas de Botucatu da UNESP during the period of January 2010 to December 2013. The group was divided by the type of medication used for induction.
A total of 90 patients were evaluated. There were no differences in baseline characteristics of age and underlying disease. The rate of biopsy-proven acute rejection was higher in the group without induction (42.9%) compared to basiliximab group (20%) and Thymoglobulin (16.7%), p = 0.04. The rejection by compatibility shows that the identical had the lower rejection rate (10%). The haploidentical group without induction had the highest rejection rates (53.3%). In all distinct group the rejection rates were similar with basiliximab or Thymoglobulin, p = NS. The use of induction therapy was associated independently with a lower risk of rejection (OR = 0.32 CI: 0.11 to 0.93, p = 0.036). There were no differences in renal function at 6 months and patient survival and graft in the three groups.
The haploidentical patients without induction were those with higher rates of acute rejection. The group of patients induced with Thymoglobulin had a higher immunological risk, however showed low rates of rejection.
The use of induction therapy resulted in lower rates of rejection in transplantation with living donor.
活体供者诱导治疗的指征尚无共识。
本研究的目的是比较不进行诱导治疗与使用胸腺球蛋白和巴利昔单抗诱导治疗对活体供者肾移植急性排斥反应发生率的影响。
我们选取了2010年1月至2013年12月期间在圣保罗州立大学博图卡图临床医院进行的所有活体供者肾移植病例。根据诱导治疗所用药物类型对该组进行划分。
共评估了90例患者。年龄和基础疾病的基线特征无差异。未进行诱导治疗组经活检证实的急性排斥反应发生率(42.9%)高于巴利昔单抗组(20%)和胸腺球蛋白组(16.7%),p = 0.04。相容性排斥反应显示,完全相同的供受者排斥率较低(10%)。未进行诱导治疗的单倍体相合组排斥率最高(53.3%)。在所有不同组中,巴利昔单抗或胸腺球蛋白组的排斥率相似,p = 无显著性差异。使用诱导治疗与较低的排斥风险独立相关(OR = 0.32,CI:0.11至0.93,p = 0.036)。三组在6个月时的肾功能、患者生存率和移植物方面无差异。
未进行诱导治疗的单倍体相合患者急性排斥反应发生率较高。接受胸腺球蛋白诱导治疗的患者免疫风险较高,但排斥率较低。
在活体供者移植中使用诱导治疗可降低排斥反应发生率。