Cytomegalovirus Infection in Seropositive Kidney Transplant Recipients With Diverse Immunological Risks Under Preemptive Strategy

医学 巨细胞病毒 免疫学 危险系数 肾移植 免疫抑制 移植 他克莫司 内科学 置信区间 病毒性疾病 病毒 疱疹病毒科
作者
Mun Chae Choi,Minyu Kang,H. Koh,Seung Hyuk Yim,Hyun Jeong Kim,Su Jin Jeong,Hyung Woo Kim,Jaeseok Yang,Beom Seok Kim,Kyu Ha Huh,Myoung Soo Kim,Juhan Lee
出处
期刊:Journal of Medical Virology [Wiley]
卷期号:97 (7)
标识
DOI:10.1002/jmv.70474
摘要

ABSTRACT Cytomegalovirus (CMV) infection remains the most prevalent viral infection in kidney transplant recipients. Despite effective preventive strategies, the use of desensitization therapies and potent immunosuppressive agents in patients with high immunological risks underscores the continued importance of CMV as a major concern. This study aims to determine the incidence and outcomes of CMV infection in patients with diverse immunological risks under preemptive stategies. We analyzed 614 CMV‐seropositive kidney transplant recipients managed under preemptive strategies. Of them, 231 patients (37.6%) underwent immunologically incompatible transplantation, including 75 ABO‐ and 156 HLA‐incompatible transplants. During the median follow‐up of 60 months, 354 patients (57.7%) experienced CMV infection. Multivariable analysis identified older recipient age, deceased donor, rituximab, and anti‐thymocyte globulin as independent risk factors for CMV infection, while the use of mammalian target of rapamycin inhibitor was protective. Multivariable Cox regression analysis confirmed that CMV infection was independently associated with increased risks of death‐censored graft loss (adjusted hazard ratio [aHR], 2.05; 95% confidence interval [CI], 1.17–3.59) and all‐cause mortality (aHR, 3.40; 95% CI, 1.60–7.23). CMV infection adversely affects graft and patient outcomes in seropositive recipients managed under preemptive strategies. These findings emphasize the need for optimized CMV prevention strategies in recipients with high immunological risks, hereby intensified preemptive strategies or immunological risk‐adapted antiviral prophylaxis are key options.
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