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肝移植后接受FK506治疗的幼儿中,爱泼斯坦-巴尔病毒感染和淋巴增殖性疾病的发病率增加。

An increased incidence of Epstein-Barr virus infection and lymphoproliferative disorder in young children on FK506 after liver transplantation.

作者信息

Cox K L, Lawrence-Miyasaki L S, Garcia-Kennedy R, Lennette E T, Martinez O M, Krams S M, Berquist W E, So S K, Esquivel C O

机构信息

Department of Transplantation, California Pacific Medical Center, San Francisco 94115.

出版信息

Transplantation. 1995 Feb 27;59(4):524-9.

PMID:7533344
Abstract

The incidence of Epstein-Barr virus (EBV) infection and lymphoproliferative disorder (LPD) was determined in a pediatric liver transplant population consisting of 51 children treated with FK506 and 91 treated with cyclosporine. The incidence of symptomatic EBV infection was 21.9% (23 of 105 cases) in children < 5 yr old and 10.8% (4 of 37 cases) in children 5 to 17 yr old as compared with 2.7% (9 of 323 cases) in adults (P < 0.0001). In the under 5 yr old group on cyclosporine, the incidences of EBV infection and LPD were 9 of 68 (13.2%) and 2 of 68 children, (2.9%), respectively. In contrast, in children under 5 yr old group on FK506, the incidences of EBV infection and LPD in the FK506 group were 14 of 37 (37.8%) and 7 of 37 children (18.9%), respectively. The difference between these two groups was statistically significant (P < 0.02). There were no cases of LPD in the 5-17 yr-old children on either cyclosporine (n = 23) or FK506 (n = 14). The incidence of EBV infections in the 5 to 17 yr age group, 17.4% on cyclosporine and 0% on FK506, was less than for the younger children on FK506 (37.8%). A total of 39% (9 of 23) of children under 5 yr old who had symptomatic EBV infections developed LPD, and 44% (4 of 9) with LPD died. The higher incidence of EBV infections and LPD in the younger children treated with FK506 was probably related to a greater intensity of immunosuppression for patients on FK506 than those on cyclosporine.

摘要

在一个儿科肝移植人群中确定了爱泼斯坦-巴尔病毒(EBV)感染和淋巴增殖性疾病(LPD)的发生率,该人群包括51名接受FK506治疗的儿童和91名接受环孢素治疗的儿童。<5岁儿童中症状性EBV感染的发生率为21.9%(105例中的23例),5至17岁儿童中为10.8%(37例中的4例),而成人中为2.7%(323例中的9例)(P<0.0001)。在5岁以下接受环孢素治疗的儿童组中,EBV感染和LPD的发生率分别为68例中的9例(13.2%)和68例儿童中的2例(2.9%)。相比之下,在5岁以下接受FK506治疗的儿童组中,FK506组中EBV感染和LPD的发生率分别为37例中的14例(37.8%)和37例儿童中的7例(18.9%)。这两组之间的差异具有统计学意义(P<0.02)。在5至17岁接受环孢素(n=23)或FK506(n=14)治疗的儿童中均无LPD病例。5至17岁年龄组中EBV感染的发生率,环孢素治疗时为17.4%,FK506治疗时为0%,低于接受FK506治疗的年幼儿童(37.8%)。共有39%(23例中的9例)有症状性EBV感染的5岁以下儿童发生了LPD,且LPD患者中有44%(9例中的4例)死亡。接受FK506治疗的年幼儿童中EBV感染和LPD的较高发生率可能与FK506治疗患者的免疫抑制强度大于环孢素治疗患者有关。

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