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肾移植受者中细小病毒B19感染相关并发症:静脉注射免疫球蛋白治疗

Parvovirus B19 infection-related complications in renal transplant recipients: treatment with intravenous immunoglobulin.

作者信息

Moudgil A, Shidban H, Nast C C, Bagga A, Aswad S, Graham S L, Mendez R, Jordan S C

机构信息

Department of Pediatrics, Cedars-Sinai Medical Center, Los Angeles, California 90048, USA.

出版信息

Transplantation. 1997 Dec 27;64(12):1847-50. doi: 10.1097/00007890-199712270-00037.

Abstract

BACKGROUND

Chronic red cell aplasia can develop in immunocompromised patients including transplant recipients infected with parvovirus B19 (PV B19). Renal involvement with PV B19 infection is not well-recognized.

METHODS

We diagnosed erythroid hypoplasia associated with PV B19 infection in three renal transplant recipients; one of them developed de novo collapsing glomerulopathy. These patients were treated with intravenous immunoglobulin (IVIG).

RESULTS

In two patients, anemia responded promptly to IVIG therapy. One of them had recurrence of anemia that responded to a second course of IVIG. Despite IVIG treatment, persistent infection with PV B19, recurrent anemia, and de novo collapsing glomerulopathy leading to allograft failure developed in the third patient, who had received the most intense immunosuppression.

CONCLUSIONS

These findings indicate that PV B19 infection in transplant recipients can cause chronic red cell aplasia that generally responds to IVIG therapy. In some patients, particularly those who are heavily immunosuppressed, infection may persist despite treatment. As the cellular receptor for PV B19 is expressed in the kidney, persistent infection may result in development of glomerulopathies in these patients.

摘要

背景

慢性红细胞再生障碍可发生于免疫功能低下的患者,包括感染细小病毒B19(PV B19)的移植受者。PV B19感染累及肾脏的情况尚未得到充分认识。

方法

我们诊断出3例肾移植受者存在与PV B19感染相关的红系造血低下;其中1例发生了新发的塌陷性肾小球病。这些患者接受了静脉注射免疫球蛋白(IVIG)治疗。

结果

2例患者的贫血对IVIG治疗迅速产生反应。其中1例贫血复发,对第二疗程的IVIG治疗有反应。尽管接受了IVIG治疗,但第三例接受了最强免疫抑制治疗的患者仍发生了PV B19持续感染、贫血复发以及导致移植肾失功的新发塌陷性肾小球病。

结论

这些发现表明,移植受者中的PV B19感染可导致慢性红细胞再生障碍,通常对IVIG治疗有反应。在一些患者中,尤其是那些免疫抑制严重的患者,尽管进行了治疗,感染仍可能持续存在。由于PV B19的细胞受体在肾脏中表达,持续感染可能导致这些患者发生肾小球病。

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