Risk Factors for Cytomegalovirus Reactivation After Liver Transplantation: Can Pre- transplant Cytomegalovirus Antibody Titers Predict Outcome?

被引:21
作者
Bruminhent, Jackrapong [1 ,6 ]
Thongprayoon, Charat [2 ]
Dierkhising, Ross A. [3 ]
Kremers, Walter K. [3 ,4 ]
Theel, Elitza S. [5 ]
Razonable, Raymund R. [1 ,4 ]
机构
[1] Mayo Clin, Dept Med, Div Infect Dis, Rochester, MN 55905 USA
[2] Mayo Clin, Dept Med, Div Crit Care Med, Rochester, MN 55905 USA
[3] Mayo Clin, Dept Hlth Sci Res, Div Biomed Stat & Informat, Rochester, MN 55905 USA
[4] Mayo Clin, William J von Liebig Ctr Transplantat & Clin Rege, Rochester, MN 55905 USA
[5] Mayo Clin, Dept Lab Med & Pathol, Div Clin Microbiol, Rochester, MN 55905 USA
[6] Mahidol Univ, Ramathibodi Hosp, Fac Med, Somdech Phra Debaratana Med Ctr, Bangkok 10400, Thailand
关键词
SEROPOSITIVE KIDNEY RECIPIENTS; SOLID-ORGAN TRANSPLANTATION; CMV INFECTION; MANAGEMENT; DISEASE; SURVIVAL; OBESITY; IMPACT; VIRUS;
D O I
10.1002/lt.24078
中图分类号
R57 [消化系及腹部疾病];
学科分类号
摘要
Despite preexisting cytomegalovirus (CMV) immunity, CMV-seropositive liver transplantation (LT) patients remain at risk of CMV infection. We hypothesized that the pre-transplant CMV antibody titer correlates with the risk of CMV reactivation. We conducted a retrospective study of CMV-seropositive LT recipients who did not receive anti-CMV prophylaxis from 2007 to 2013. The pre-transplant CMV immunoglobulin G (IgG) titer, which was measured with an enzyme-linked fluorescent immunoassay, was assessed as a risk factor for CMV reactivation with multivariate Cox proportional hazards models. The population consisted of 225 CMV-seropositive LT patients with a median age of 57 years (interquartile range, 47-62 years). The CMV titer distributions were as follows: <60 (40%) and 60 AU/mL (60%). The Kaplan-Meier estimates for CMV infection were 17% at 3 months, 18% at 6 months, and 19% at 12 months after transplantation. In a univariate analysis, a marginally significant increased risk of CMV infection was seen in LT recipients with a pre-transplant CMV IgG titer<60 AU/mL versus60 AU/mL [hazard ratio (HR), 1.79; 95% confidence interval (CI), 0.98-3.28 (P = 0.06)]. This risk was statistically significant in the subgroup of recipients who received allografts from CMV-seropositive donors [HR, 2.21; 95% CI, 1.15-4.26 (P = 0.02)]. In a multivariate analysis, a pre-transplant CMV IgG titer<60 AU/mL was significantly associated with CMV infection [HR, 3.11; 95% CI, 1.60-6.03 (P<0.001)]. The other risk factors were high body mass index, donor CMV seropositivity, prolonged cold ischemic time, use of an interleukin-2 receptor antagonist for induction therapy, and high numbers of post-transplant infections. A lower pre-transplant CMV antibody titer is significantly associated with CMV infection after LT. Quantitative measurement of CMV-specific humoral immunity may have a potential role in improving the CMV prevention strategy in CMV-seropositive LT recipients. Liver Transpl 21:539-546, 2015. (c) 2015 AASLD.
引用
收藏
页码:539 / 546
页数:8
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