细小病毒B19在肝、肾和胰腺移植候选者中的状况:单一中心经验

Bojana Simunov, Anna Mrzljak, Zeljka Jurekovic, Snjezana Zidovec Lepej, Ana Bainrauch, Jadranka Pavicic Saric, Zeljka Hruskar, Leona Radmanic, Tatjana Vilibic-Cavlek
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引用次数: 0

摘要

背景:细小病毒B19 (B19V)与广泛的临床表现相关。主要表现为感染性红斑。然而,持续感染可能导致免疫功能低下患者的纯红细胞发育不全和慢性贫血。B19V血清阳性率随年龄和地理位置的不同而不同。目的:测定肾、肝、胰移植候选者的B19V血清学状态和dna血症。方法:在2021年1月至2022年5月期间接受肾脏、肝脏或同时进行肾脏和胰腺/肝脏移植的患者纳入研究。移植前采集血清样本。检测B19V DNA时,使用LightMix Kit B19V EC (TIB MOLBIOL, Berlin, Germany)。B19V IgM和IgG抗体采用商用ELISA检测(euroimmune, l beck,德国)。结果:131例移植候选者纳入研究,男性占71.0%,平均年龄53.27岁±12.71岁。肝移植占68.7%,肾移植占27.5%,胰肾联合移植(SPKT)占3.0%,肝肾联合移植占0.8%。没有患者检测到B19V DNA。血清B19V IgG阳性率为77.1%。未发现急性或近期感染(IgM抗体)。血清阴性和血清阳性患者的平均年龄无差异(51.8岁±12.9岁vs 53.7岁±12.7岁,t = -0.603;P = 0.548)。虽然30岁以下患者血清阳性率(66.6%)低于30-59岁和> 60岁患者(分别为80.4%和78.1%),但差异不显著。此外,男性和女性移植候选者血清阳性无差异,分别为76.3%和78.9% (χ 2 = 0.104;P = 0.748)。不同器官受体的血清阳性率无差异,肝脏、肾脏和SPKT分别为77.8%、80.6%和50.0%,(χ 2 = 5.297;P = 0.151)。不同透析方式肾移植患者血清阳性率差异无统计学意义。血透患者血清阳性率为71.1%,腹膜透析患者血清阳性率为100% (χ 2 = 0.799;P = 0.372)。结论:B19V血清阳性率在肾、肝和胰腺移植候选人群中预期较高,但仍有22.9%的血清阴性个体仍有原发性疾病和严重症状的风险。进一步的研究应阐明B19V筛查在移植围期管理中的必要性。
本文章由计算机程序翻译,如有差异,请以英文原文为准。

Parvovirus B19 status in liver, kidney and pancreas transplant candidates: A single center experience.

Parvovirus B19 status in liver, kidney and pancreas transplant candidates: A single center experience.

Background: Parvovirus B19 (B19V) is associated with a wide range of clinical manifestations. The major presentation is erythema infectiosum. However, a persistent infection may cause pure red cell aplasia and chronic anemia in immunocompromized patients. The B19V seroprevalence varies with age and geographical location.

Aim: To determine the B19V serological status and DNAemia in kidney, liver, and pancreas transplant candidates.

Methods: Patients who underwent kidney, liver, or simultaneous kidney and pancreas/liver transplantation between January 2021 and May 2022 were included in the study. The serum samples were collected before transplantation. For detection of B19V DNA, a LightMix Kit B19V EC (TIB MOLBIOL, Berlin, Germany) was used. B19V IgM and IgG antibodies were detected using a commercial ELISA test (Euroimmun, Lübeck, Germany).

Results: One hundred and thirty-one transplant candidates were included in the study, 71.0% male, with an average age of 53.27 years ± 12.71 years. There were 68.7% liver, 27.5% kidney, 3.0% simul taneous pancreas/kidney transplant (SPKT), and 0.8% simultaneous liver/kidney transplant recipients. No patients had detectable B19V DNA. B19V IgG seroprevalence was 77.1%. No acute or recent infections were detected (IgM antibodies). There was no difference in the mean age of seronegative and seropositive patients (51.8 years ± 12.9 years vs 53.7 years ± 12.7 years, t = -0.603; P = 0.548). Although seropositivity was lower in patients aged less than 30 years (66.6%) compared to the patients aged 30-59 years and > 60 years (80.4% and 78.1%, respectively), this difference was not significant. In addition, there was no difference in seropositivity between male and female transplant candidates, 76.3% and 78.9% (χ 2 = 0.104; P = 0.748). The seroprevalence did not differ among organ recipients, with 77.8%, 80.6%, and 50.0% for liver, kidney, and SPKT, respectively, (χ 2 = 5.297; P = 0.151). No significant difference was found in the seroprevalence in kidney transplant patients according to dialysis modality. Seroprevalence was 71.1% in hemodialysis patients, and 100% in peritoneal dialysis patients (χ 2 = 0.799; P = 0.372).

Conclusion: The B19V seroprevalence is expectedly high among kidney, liver, and pancreas transplant candidates, but there are still 22.9% of seronegative individuals who remain at risk for primary disease and severe manifestations. Further research should elucidate the necessity of B19V screening in peri-transplant management.

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