首页> 外文期刊>American Journal of Transplantation >BK Virus-Specific Immunity Kinetics: A Predictor of Recovery From Polyomavirus BK-Associated Nephropathy
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BK Virus-Specific Immunity Kinetics: A Predictor of Recovery From Polyomavirus BK-Associated Nephropathy

机译:BK病毒特异性免疫动力学:从多瘤病毒BK相关的肾病中恢复的预测因子。

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Impaired BKV-specific immunity is associated with development of BKV-associated nephropathy. Suitable immunological parameters to identify patients at risk, however, are still debated. We monitored 18 kidney-transplant recipients through the course of self-limited BKV-reactivation (n = 11) and BKV-associated nephropathy (n = 7). BKV-specific cellular immunity directed to nonstructural small and Large T-antigen, and structural VP1–3 was analyzed in an interferon- Elispot assay. BKV-specific IgM and IgG were measured using an enzyme-linked immunosorbent assay simultaneously. BKV-specific cellular immunity directed to five BKV-proteins increased significantly from diagnosis to resolution of BKV-reactivation (p < 0.001). Patients with self-limited BKV-reactivation developed BKV-specific T cells without therapeutic interventions, and cleared BKV-reactivation within a median period of 1 month. Patients with BKV-associated nephropathy, however, showed BKV-specific T cells after a median period of 5 months after therapeutic interventions only, and cleared BKV-reactivation after a median period of 8 months. Anti-structural T cells were detected earlier than anti-nonstructural T cells, which coincided with BKV-clearance. Patients with BKV-associated nephropathy showed the highest frequencies of BKV-specific T cells at recovery, the highest increase in BKV-specific IgG and persistence of increased IgM levels (p < 0.05). Our results suggest prognostic values of BKV-specific immune monitoring to identify those patients at risk of BKV-associated nephropathy and to aid in the management of therapeutic interventions.
机译:BKV特异性免疫受损与BKV相关性肾病的发展有关。但是,仍在争论用于确定高危患者的合适免疫学参数。我们通过自我限制的BKV激活(n = 11)和BKV相关的肾病(n = 7)的过程监测了18位肾脏移植接受者。 BKV特异性针对非结构性大和小的T抗原的细胞免疫,以及结构VP1-3在干扰素Elispot分析中进行了分析。同时使用酶联免疫吸附测定法测量BKV特异性IgM和IgG。从诊断到BKV激活的消退,针对五种BKV蛋白的BKV特异性细胞免疫显着提高(p <0.001)。具有自我限制的BKV激活的患者无需治疗即可产生BKV特异性T细胞,并在1个月的中位时间内清除BKV激活。然而,患有BKV相关性肾病的患者仅在治疗干预后5个月的中位时间后显示BKV特异性T细胞,并且在8个月的中位时间后清除BKV重新激活。检测到的抗结构性T细胞要早于抗非结构性T细胞,这与BKV清除率相吻合。与BKV相关的肾病患者在恢复时显示BKV特异性T细胞的频率最高,BKV特异性IgG的增加最高,并且IgM水平持续升高(p <0.05)。我们的研究结果提示了BKV特异性免疫监测的预后价值,以识别有BKV相关性肾病风险的患者并协助治疗干预措施的管理。

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