van Saase J L, van der Woude F J, Thorogood J, Hollander A A, van Es L A, Weening J J, van Bockel J H, Bruijn J A
Department of Nephrology, Leiden University Hospital, The Netherlands.
Transplantation. 1995 May 15;59(9):1280-5.
Chronic rejection of renal allografts is a major cause of late graft loss. However, time of onset, relation with acute early rejection episodes, and risk factors are largely unknown. We undertook a cohort study of 482 consecutive patients from a single center who received a cadaveric renal allograft between January 1983 and April 1991. During the first 3 months after transplantation, 76 (15.8%) patients developed vascular rejection and 115 (23.9%) developed interstitial rejection. One-year graft survival of patients without rejection, with interstitial rejection, and with vascular rejection was 87.8%, 87%, and 48.7%, respectively. Five-year graft survival was 73.5% for the group without rejection, 71.4% for patients with interstitial rejection, and 34.3% for patients with vascular rejection. The adjusted relative risk of graft loss was 4.92 (95% CI 3.25-7.43) for patients with vascular rejection and 1.27 (95% CI 0.80-2.02) for patients with interstitial rejection compared with patients without early rejection, taking the time dependency of the rejection events and prognostic factors into account. The incidence of vascular rejection was increased in patients with primary nonfunction (RR 1.69, 95% CI 1.01-2.84), with 1 HLA-DR mismatch (RR 2.38, 95% CI 1.44-3.93), with 2 HLA-DR mismatches (RR 3.24, 95% CI 1.25-8.42), with a prolonged cold ischemia time (RR 1.03, 95% CI 1.00-1.06 per hr), and with 1 or more previous transplantations (RR 1.76, 95% CI 1.01-3.07). Risk of developing vascular rejection was decreased in patients using CsA as compared with azathioprine (RR 0.41, 95% CI 0.24-0.67). Early vascular rejection, occurring within 3 months after transplantation, is the most important predicting variable of both early and late graft loss. Use of CsA, less HLA-DR mismatching, and a cold ischemia time of short duration possibly prevent the development of vascular rejection.
肾移植慢性排斥是移植肾晚期丢失的主要原因。然而,其发病时间、与急性早期排斥反应的关系以及危险因素在很大程度上尚不清楚。我们对1983年1月至1991年4月间在单一中心接受尸体肾移植的482例连续患者进行了一项队列研究。在移植后的前3个月,76例(15.8%)患者发生血管性排斥反应,115例(23.9%)发生间质性排斥反应。无排斥反应、发生间质性排斥反应和发生血管性排斥反应患者的1年移植肾存活率分别为87.8%、87%和48.7%。无排斥反应组的5年移植肾存活率为73.5%,间质性排斥反应患者为71.4%,血管性排斥反应患者为34.3%。与无早期排斥反应的患者相比,考虑到排斥反应事件和预后因素的时间依赖性,血管性排斥反应患者移植肾丢失的校正相对风险为4.92(95%CI 3.25 - 7.43),间质性排斥反应患者为1.27(95%CI 0.80 - 2.02)。原发性无功能患者(RR 1.69,95%CI 1.01 - 2.84)、有1个HLA - DR错配患者(RR 2.38,95%CI 1.44 - 3.93)、有2个HLA - DR错配患者(RR 3.24,95%CI 1.25 - 8.42)、冷缺血时间延长患者(RR 1.03,95%CI每小时1.00 - 1.06)以及有1次或更多次既往移植患者(RR 1.76,95%CI 1.01 - 3.07)发生血管性排斥反应的发生率增加。与使用硫唑嘌呤相比,使用环孢素A的患者发生血管性排斥反应的风险降低(RR 0.41,95%CI 0.24 - 0.67)。移植后3个月内发生的早期血管性排斥反应是早期和晚期移植肾丢失的最重要预测变量。使用环孢素A、减少HLA - DR错配以及缩短冷缺血时间可能预防血管性排斥反应的发生。