Human Cytomegalovirus Infection Induces Long-Term Changes in the Cytokine Milieu of Kidney Transplant Recipients.

IF 6.8 3区 医学 Q1 VIROLOGY Journal of Medical Virology Pub Date : 2025-01-01 DOI:10.1002/jmv.70178
Natalia Redondo, Andrea Valverde-Manso, Tamara Ruiz-Merlo, Isabel Rodríguez-Goncer, Patricia Parra, Francisco López-Medrano, Esther González, Natalia Polanco, Rafael San Juan, Amado Andrés, José María Aguado, Mario Fernández-Ruiz
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Abstract

The impact of human cytomegalovirus (HCMV) infection on the mid- and long-term balance between pro-inflammatory and anti-inflammatory cytokines among kidney transplant recipients (KTRs) remains unclear. We measured plasma levels of 12 Th1/Th2-type cytokines (granulocyte-macrophage colony-stimulating factor, interferon-γ, interleukin [IL]-1β, IL-2, IL-4, IL-5, IL-6, IL-10, IL-12p70, IL-13, IL-18 and tumor necrosis factor-α) in a cohort of 290 KTRs at four time points through month 12 after transplantation. Cytokine levels at each point were compared according to the previous documentation of HCMV replication by two approaches: "cumulative exposure" from the time of transplantation and "recent exposure" within the 2-3 months preceding cytokine assessment. Significance levels were Bonferroni-corrected for multiple pairwise comparisons. Plasma levels of IL-6, IL-10, and IL-12p70 at month 1 were significantly increased in KTRs that had experienced HCMV infection during the first 30 days. By month 3, IL-6 and IL-10 remained increased in KTRs with cumulative exposure through day 90. Cumulative exposure to HCMV replication through day 180 was also associated to increased IL-10 levels at month 6. In addition, KTRs with recent HCMV exposure had increased IL-10 levels at months 3 and 6. After multivariable adjustment, cumulative exposure to HCMV infection and/or the area under curve of HCMV DNAemia during the corresponding period were associated to IL-10 levels within the highest quartile at months 1, 3, and 6. Preceding HCMV infection induces sustained changes in the plasma cytokine milieu of KTRs, with elevated IL-6 and IL-10 levels throughout the first 6 months after transplantation.

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人巨细胞病毒感染诱导肾移植受者细胞因子环境的长期变化。
人巨细胞病毒(HCMV)感染对肾移植受者(KTRs)中促炎和抗炎细胞因子中长期平衡的影响尚不清楚。我们在移植后12个月的4个时间点测量了290名ktr患者血浆中12种Th1/ th2型细胞因子(粒细胞-巨噬细胞集落刺激因子、干扰素-γ、白细胞介素[IL]-1β、IL-2、IL-4、IL-5、IL-6、IL-10、IL-12p70、IL-13、IL-18和肿瘤坏死因子-α)的水平。根据先前的HCMV复制记录,通过两种方法比较每个点的细胞因子水平:移植时的“累积暴露”和细胞因子评估前2-3个月内的“最近暴露”。多重两两比较的显著性水平采用bonferroni校正。在头30天内经历HCMV感染的ktr患者中,第1个月时血浆IL-6、IL-10和IL-12p70水平显著升高。到第3个月,IL-6和IL-10在KTRs中持续升高,累积暴露到第90天。通过180天的HCMV复制累积暴露也与第6个月时IL-10水平升高有关。此外,最近暴露于HCMV的KTRs在第3和6个月时IL-10水平升高。在多变量调整后,在相应时期,HCMV感染的累积暴露和/或HCMV dna血症曲线下面积与1,3,6个月最高四分位数内的IL-10水平相关。先前的HCMV感染诱导KTRs血浆细胞因子环境的持续变化,在移植后的前6个月内IL-6和IL-10水平升高。
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来源期刊
Journal of Medical Virology
Journal of Medical Virology 医学-病毒学
CiteScore
23.20
自引率
2.40%
发文量
777
审稿时长
1 months
期刊介绍: The Journal of Medical Virology focuses on publishing original scientific papers on both basic and applied research related to viruses that affect humans. The journal publishes reports covering a wide range of topics, including the characterization, diagnosis, epidemiology, immunology, and pathogenesis of human virus infections. It also includes studies on virus morphology, genetics, replication, and interactions with host cells. The intended readership of the journal includes virologists, microbiologists, immunologists, infectious disease specialists, diagnostic laboratory technologists, epidemiologists, hematologists, and cell biologists. The Journal of Medical Virology is indexed and abstracted in various databases, including Abstracts in Anthropology (Sage), CABI, AgBiotech News & Information, National Agricultural Library, Biological Abstracts, Embase, Global Health, Web of Science, Veterinary Bulletin, and others.
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