Cytomegalovirus infection after acute rejection therapy in seropositive kidney transplant recipients

被引:19
作者
Lee, Y. -M. [1 ,2 ]
Kim, Y. H. [3 ]
Han, D. J. [3 ]
Park, S. -K. [4 ]
Park, J. S. [4 ]
Sung, H. [5 ]
Hong, H. -L. [1 ]
Kim, T. [1 ]
Kim, S. -H. [1 ]
Choi, S. -H. [1 ]
Kim, Y. S. [1 ]
Woo, J. H. [1 ]
Lee, S. -O. [1 ]
机构
[1] Univ Ulsan, Dept Infect Dis, Asan Med Ctr, Coll Med, Seoul 138736, South Korea
[2] Inje Univ, Coll Med, Dept Infect Dis, Busan Paik Hosp, Pusan, South Korea
[3] Univ Ulsan, Dept Surg, Asan Med Ctr, Coll Med, Seoul 138736, South Korea
[4] Univ Ulsan, Dept Nephrol, Asan Med Ctr, Coll Med, Seoul 138736, South Korea
[5] Univ Ulsan, Dept Lab Med, Asan Med Ctr, Coll Med, Seoul 138736, South Korea
关键词
acute rejection; cytomegalovirus infection; kidney transplantation; PREEMPTIVE GANCICLOVIR THERAPY; ALLOGRAFT-REJECTION; DISEASE; PROPHYLAXIS; SOCIETY;
D O I
10.1111/tid.12227
中图分类号
R392 [医学免疫学]; Q939.91 [免疫学];
学科分类号
100102 ;
摘要
Background Acute rejection (AR) after solid organ transplantation has been known to be a risk factor for cytomegalovirus (CMV) infection. However, data regarding the risk for CMV infection during and after anti-rejection therapy are limited. This study investigated whether the risk of CMV infection and disease within 6months of kidney transplantation (KT) increases in CMV-seropositive KT recipients who develop AR. Methods A total of 992 seropositive KT recipients, including 75 patients (8%) who developed AR within 6months after KT and 917 patients (92%) who did not, were recruited between May 2007 and April 2012. Results No significant difference was found in the incidence of CMV infection between the groups (AR group, 13% [10/75] vs. non-AR group, 10% [92/917], P=0.37). The number of KT recipients in each group receiving preemptive therapy for CMV was similar (5% [4/75] vs. 6% [53/917], 0.99). While the incidence of CMV syndrome was comparable (0% [0/75] vs. 1% [12/917], 0.99), the incidence of tissue-invasive CMV disease (8% [6/75] vs. 3% [27/917], P=0.04), particularly gastrointestinal CMV disease, was significantly greater in patients who experienced AR. No CMV-related mortality occurred in either group. AR (odds ratio, 2.81; 95% confidence interval, 1.08-7.29; P=0.03) was an independent risk factor for tissue-invasive CMV disease within 6months of KT. Conclusions A high index of suspicion and active evaluation for tissue-invasive CMV disease in KT recipients suffering AR may be necessary to ensure appropriate treatment.
引用
收藏
页码:397 / 402
页数:6
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