Moon Hyung Hwan, Kim Tae-Seok, Lee Sanghoon, Song Sanghyun, Shin Milljae, Park Jae Berm, Kim Jong Man, Jang Hye Ryoun, Huh Wooseong, Joh Jae-Won, Kim Sung Joo
Departments of Surgery, Samsung Medical Center, Sungkyunkwan University School of Medicine, Seoul, Korea.
Division of Nephrology, Department of Medicine, Samsung Medical Centre, Sungkyunkwan University School of Medicine, Seoul, Korea.
Cent Eur J Immunol. 2014;39(1):96-9. doi: 10.5114/ceji.2014.42132. Epub 2014 Apr 17.
The ImmuKnow assay (cylex Inc., Columbia, MD) has been reported to measure the global immune monitoring tool for organ transplantation recipients. We assess immuKnow ATP values in stable kidney transplant patients.
Patients who were kidney transplanted between September 2008 and May 2011 were enrolled in the prospective serial ImmuKnow assay study. The criteria of inclusion were living donor kidney transplantation (KT), no evidence of hepatitis B virus (HBV) and hepatitis C virus (HCV) infection, and PRA less than 50%. ImmuKnow assay monitoring was performed at one day before operation, post operative weeks 4, 8, 12, 16, 20, 24, 36 and 52. We excluded patients who had undergone infectious syndrome or rejection episodes during the follow-up period.
Among 71 patients who were enrolled in prospective serial ImmuKnow assay monitoring, 37 patients were proven to stable KT patients during the follow-up period. Two hundred and twenty-four samples from 37 patients were collected. ImmuKnow value and immunosuppression drug level were compared in post operative weeks 4, 8, 12, 16, 20, 24, 36 and 52. The value of ImmuKnow assay was significantly different depending on the length of time after transplant (p = 0.038). Interestingly, the pre-transplant ImmuKnow values were lower than those of the immediate post-transplant period.
The ImmuKnow value of stable KT recipients is different according to "time after transplant". Therefore, "time after transplant" should be considered when applying an ImmuKnow assay in clinical practice.
据报道,免疫状态监测分析(Cylex公司,哥伦比亚,马里兰州)可用于测量器官移植受者的整体免疫监测工具。我们评估稳定肾移植患者的免疫状态监测分析ATP值。
将2008年9月至2011年5月间接受肾移植的患者纳入前瞻性系列免疫状态监测分析研究。纳入标准为活体供肾移植(KT),无乙肝病毒(HBV)和丙肝病毒(HCV)感染证据,且群体反应性抗体(PRA)低于50%。在术前一天、术后第4、8、12、16、20、24、36和52周进行免疫状态监测分析。我们排除了在随访期间发生感染综合征或排斥反应的患者。
在纳入前瞻性系列免疫状态监测分析的71例患者中,37例在随访期间被证明为稳定的肾移植患者。收集了37例患者的224份样本。比较了术后第4、8、12、16、20、24、36和52周的免疫状态监测分析值和免疫抑制药物水平。免疫状态监测分析值因移植后时间长短而异(p = 0.038)。有趣的是,移植前的免疫状态监测分析值低于移植后即刻的值。
稳定肾移植受者的免疫状态监测分析值因“移植后时间”而异。因此,在临床实践中应用免疫状态监测分析时应考虑“移植后时间”。