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肺移植中巨细胞病毒(CMV)的 QuantiFERON CMV 检测和血清学状态:感染、慢性和急性移植物排斥反应的分层风险。

QuantiFERON CMV Test and CMV Serostatus in Lung Transplant: Stratification Risk for Infection, Chronic and Acute Allograft Rejection.

机构信息

Division of Respiratory Medicine, Cardiovascular and Thoracic Department, AOU Città della Salute e della Scienza di Torino, 10126 Torino, Italy.

Medical Sciences Department, University of Turin, 10126 Torino, Italy.

出版信息

Viruses. 2024 Aug 4;16(8):1251. doi: 10.3390/v16081251.

DOI:10.3390/v16081251
PMID:39205225
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC11358887/
Abstract

The QuantiFERON CMV (QCMV) test evaluates specific adaptive immune system activity against CMV by measuring IFN-γ released by activated CD8+ T lymphocytes. We aimed to evaluate the QCMV test as a predictive tool for CMV manifestations and acute or chronic lung allograft rejection (AR and CLAD) in lung transplant (LTx) patients. A total of 73 patients were divided into four groups based on donor and recipient (D/R) serology for CMV and QCMV assay: group A low-risk for CMV infection and disease (D-/R-); group B and C at intermediate-risk (R+), group B with non-reactive QCMV and group C with reactive QCMV; group D at high-risk (D+/R-). Group D patients experienced higher viral replication; no differences were observed among R+ patients of groups B and C. D+/R- patients had a higher number of AR events and group C presented a lower incidence of AR. Prevalence of CLAD at 24 months was higher in group B with a higher risk of CLAD development (OR 6.33). The QCMV test allows us to identify R+ non-reactive QCMV population as the most exposed to onset of CLAD. This population had a higher, although non-significant, susceptibility to AR compared to the R+ population with reactive QCMV.

摘要

QuantiFERON CMV(QCMV)检测通过测量活化的 CD8+T 淋巴细胞释放的 IFN-γ,评估针对 CMV 的特定适应性免疫系统活性。我们旨在评估 QCMV 检测作为肺移植(LTx)患者 CMV 表现以及急性或慢性肺移植物排斥(AR 和 CLAD)的预测工具。共有 73 名患者根据 CMV 的供体和受体(D/R)血清学和 QCMV 检测结果分为四组:A 组为 CMV 感染和疾病低风险(D-/R-);B 组和 C 组为中风险(R+),B 组 QCMV 无反应,C 组 QCMV 有反应;D 组为高风险(D+/R-)。D 组患者的病毒复制水平更高;B 组和 C 组的 R+患者之间没有观察到差异。D+/R-患者的 AR 事件更多,C 组的 AR 发生率较低。B 组 24 个月时 CLAD 的患病率更高,发展为 CLAD 的风险更高(OR 6.33)。QCMV 检测可识别 R+无反应 QCMV 人群,该人群发生 CLAD 的风险最高。与 R+有反应 QCMV 人群相比,该人群的 AR 易感性虽然没有统计学意义,但更高。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/b220/11358887/2f06351ced5c/viruses-16-01251-g002.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/b220/11358887/222b5781a5f3/viruses-16-01251-g001.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/b220/11358887/2f06351ced5c/viruses-16-01251-g002.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/b220/11358887/222b5781a5f3/viruses-16-01251-g001.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/b220/11358887/2f06351ced5c/viruses-16-01251-g002.jpg

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3
Revisiting cytomegalovirus serostatus and replication as risk factors for inferior long-term outcomes in the current era of renal transplantation.
重新探讨巨细胞病毒血清学状态和复制作为当前肾移植时代长期预后不良的风险因素。
Nephrol Dial Transplant. 2020 Feb 1;35(2):346-356. doi: 10.1093/ndt/gfz268.
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Tailored combined cytomegalovirus management in lung transplantation: a retrospective analysis.肺移植中定制的巨细胞病毒管理:回顾性分析。
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Chronic lung allograft dysfunction: Definition, diagnostic criteria, and approaches to treatment-A consensus report from the Pulmonary Council of the ISHLT.慢性肺移植功能障碍:定义、诊断标准及治疗方法——国际心肺移植学会肺委员会共识报告
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