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超越血清学,对移植受者的 CMV 感染风险进行分层。

Going beyond serology for stratifying the risk of CMV infection in transplant recipients.

机构信息

Microbiology Service, Hospital Clínico Universitario, Fundación INCLIVA, Valencia, Spain.

Unit of Infectious Diseases, Hospital Universitario "12 de Octubre", Instituto de Investigación Hospital,"12 de Octubre" (i+12), School of Medicine, Universidad Complutense, Madrid, Spain.

出版信息

Rev Med Virol. 2019 Jan;29(1):e2017. doi: 10.1002/rmv.2017. Epub 2018 Oct 25.

Abstract

Knowledge of donor and recipient (D/R) cytomegalovirus (CMV) serostatus is critical for risk stratification of CMV infection and disease in transplant recipients, particularly in the solid organ transplantation (SOT) setting. Despite its broad availability and the success of it use, the risk stratification based on the D/R serostatus is not free of limitations since there are a nondepreciable number of patients that are not accurately categorized by this approach. In fact, up to 20% of seropositive SOT recipients, classically considered at intermediate risk, develop episodes of CMV infection and disease after transplantation. Here, we provide an overview of additional donor and recipient factors that may have utility in identifying patients at risk for post-transplant CMV infection. Specifically, we summarize our current understanding regarding the potential use of use CMV-specific T-cell-mediated immunity, neutralizing antibodies and host genetics that may influence the risk of CMV infection and disease. We provide an overview of the benefits and limitations associated with using these immunological factors in risk stratification and propose specific variables that could be analyzed at the pretransplant evaluation to improve the identification of patients with increased individual susceptibility.

摘要

了解供体和受者(D/R)巨细胞病毒(CMV)血清状态对于移植受者 CMV 感染和疾病的风险分层至关重要,特别是在实体器官移植(SOT)环境中。尽管 CMV 特异性 T 细胞介导的免疫、中和抗体和宿主遗传学等因素可能影响 CMV 感染和疾病的风险,但基于 D/R 血清状态的风险分层并非没有局限性,因为仍有相当数量的患者无法通过这种方法准确分类。事实上,高达 20%的经典中间风险的 SOT 受者在移植后会出现 CMV 感染和疾病。在这里,我们概述了其他供体和受者因素,这些因素可能有助于识别移植后 CMV 感染的风险患者。具体来说,我们总结了我们目前对 CMV 特异性 T 细胞介导的免疫、中和抗体和宿主遗传学在识别 CMV 感染和疾病风险中的潜在用途的理解。我们概述了在风险分层中使用这些免疫因素的益处和局限性,并提出了在移植前评估中可以分析的具体变量,以提高对个体易感性增加的患者的识别能力。

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