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移植前 pp65 特异性 CD4 T 细胞反应评估可识别接受 rATG 治疗的 CMV 血清阳性患者发生迟发性感染的风险。

Pre-transplant assessment of pp65-specific CD4 T cell responses identifies CMV-seropositive patients treated with rATG at risk of late onset infection.

机构信息

Nephrology service, La Paz University Hospital, Madrid, Spain.

Institute for Health Research Hospital Universitario La Paz - IdiPAZ, Paseo Castellana 261, 28046 Madrid, Spain.

出版信息

Clin Immunol. 2020 Feb;211:108329. doi: 10.1016/j.clim.2019.108329. Epub 2019 Dec 28.

Abstract

Assessment of CMV-specific T cell immunity might be a useful tool in predicting CMV infection after solid organ transplantation. We have investigated CD4 and CD8 T-cell responses to CMV pp65 and IE-1 antigens in a prospective study of 28 CMV-seropositive kidney transplant recipients who were administered lymphocyte-depleting antibodies (Thymoglobulin®) as induction treatment and with universal prophylaxis for CMV infection. The response was analyzed by intracellular flow cytometry analysis of IFN-γ production in pretransplant samples and at 1, 6, 12 and 24 months post-transplant. Overall, only pretransplant CD4 T-cell responses to pp65 were significantly lower (p = .004) in patients with CMV replication post-transplant. ROC curve analysis showed that pre-transplant frequencies of pp65-specific CD4 + T cells below 0.10% could predict CMV infection with 75% sensitivity and 83.33% specificity (AUC: 0.847; 95% CI: 0.693-1.001; p = .0054) and seem to be mandatory for efficient control of CMV viral replication by the host immune system. In conclusion, the functional assessment of CMV-specific CD4 T-cell immunity pretransplant in seropositive patients may allow the identification of Thymoglobulin®-treated kidney transplant recipients at risk of developing CMV infection post-transplantation.

摘要

评估 CMV 特异性 T 细胞免疫可能是预测实体器官移植后 CMV 感染的有用工具。我们在一项前瞻性研究中调查了 28 例 CMV 血清阳性的肾移植受者的 CD4 和 CD8 T 细胞对 CMV pp65 和 IE-1 抗原的反应,这些受者接受了淋巴细胞耗竭抗体(Thymoglobulin®)作为诱导治疗,并进行了 CMV 感染的普遍预防。通过在移植前样本和移植后 1、6、12 和 24 个月时产生 IFN-γ的细胞内流式细胞术分析来分析反应。总体而言,只有移植后发生 CMV 复制的患者的移植前 pp65 特异性 CD4 T 细胞反应明显较低(p=0.004)。ROC 曲线分析表明,移植前 pp65 特异性 CD4+T 细胞频率低于 0.10%可预测 CMV 感染,具有 75%的敏感性和 83.33%的特异性(AUC:0.847;95%CI:0.693-1.001;p=0.0054),并且似乎是宿主免疫系统有效控制 CMV 病毒复制所必需的。总之,在血清阳性患者中移植前对 CMV 特异性 CD4 T 细胞免疫的功能评估可能允许识别接受 Thymoglobulin®治疗的肾移植受者,这些受者在移植后有发生 CMV 感染的风险。

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