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本文引用的文献

1
Immune reconstitution and survival of patients with parvovirus B19 related pure red cell aplasia after haplo-PBSCT.单倍体 PBSCT 后微小病毒 B19 相关纯红细胞再生障碍患者的免疫重建和存活。
Ann Hematol. 2022 Jun;101(6):1333-1342. doi: 10.1007/s00277-022-04831-w. Epub 2022 Apr 9.
2
[The hematological diversity of human parvovirus B19 infection after allo-hematopoietic stem cell transplantation in pediatric patients].[小儿患者异基因造血干细胞移植后人类细小病毒B19感染的血液学多样性]
Zhonghua Xue Ye Xue Za Zhi. 2021 Aug 14;42(8):654-659. doi: 10.3760/cma.j.issn.0253-2727.2021.08.007.
3
Infections with DNA Viruses, Adenovirus, Polyomaviruses, and Parvovirus B19 in Hematopoietic Stem Cell Transplant Recipients and Patients with Hematologic Malignancies.造血干细胞移植受者和血液恶性肿瘤患者中 DNA 病毒、腺病毒、多瘤病毒和细小病毒 B19 的感染。
Infect Dis Clin North Am. 2019 Jun;33(2):501-521. doi: 10.1016/j.idc.2019.02.005. Epub 2019 Mar 30.
4
Parvovirus B19 Infection.细小病毒B19感染
N Engl J Med. 2018 Dec 13;379(24):2361. doi: 10.1056/NEJMicm1807156.
5
Human Parvoviruses.人类细小病毒
Clin Microbiol Rev. 2017 Jan;30(1):43-113. doi: 10.1128/CMR.00040-16.
6
[The consensus of allogeneic hematopoietic transplantation for hematological diseases in China (2014)--indication, conditioning regimen and donor selection].《中国造血干细胞移植治疗血液系统疾病专家共识(2014版)——适应证、预处理方案及供者选择》
Zhonghua Xue Ye Xue Za Zhi. 2014 Aug;35(8):775-80. doi: 10.3760/cma.j.issn.0253-2727.2014.08.029.
7
Persistent parvovirus B19 infection resulting in red cell aplasia after allogeneic hematopoietic stem cell transplantation.异基因造血干细胞移植后持续性细小病毒B19感染导致红细胞再生障碍。
Transpl Infect Dis. 2013 Dec;15(6):E239-42. doi: 10.1111/tid.12155. Epub 2013 Oct 18.
8
Low-level DNAemia of parvovirus B19 (genotypes 1-3) in adult transplant recipients is not associated with anaemia.在成年移植受者中,细小病毒 B19(基因型 1-3)的低水平 DNAemia 与贫血无关。
J Clin Virol. 2013 Oct;58(2):443-8. doi: 10.1016/j.jcv.2013.07.007. Epub 2013 Jul 31.
9
Human parvoviruses B19, PARV4 and bocavirus in pediatric patients with allogeneic hematopoietic SCT.人细小病毒 B19、PARV4 和 bocavirus 在异基因造血干细胞移植的儿科患者中的情况。
Bone Marrow Transplant. 2013 Oct;48(10):1308-12. doi: 10.1038/bmt.2013.63. Epub 2013 May 20.
10
[Association of human parvovirus B19 infection and childhood idiopathic thrombocytopenic purpura: a meta analysis of Chinese literatures].[人类细小病毒B19感染与儿童特发性血小板减少性紫癜的相关性:中文文献的Meta分析]
Zhongguo Dang Dai Er Ke Za Zhi. 2009 Dec;11(12):999-1001.

异基因造血干细胞移植后人类细小病毒B19感染的临床特征

[Clinical characteristics of human parvovirus B19 infection after allogeneic stem cell transplantation].

作者信息

Zhang J, Ma R, Luo X Y, Zhang X H, Xu L P, Wang Y, Mo X D, Lyu M, Liu K Y, Huang X J, Sun Y Q

机构信息

Peking University People's Hospital, Peking University Institute of Hematology, National Clinical Research Center for Hematologic Disease, Beijing Key Laboratory of Hematopoietic Stem Cell Transplantation, Beijing 100044, China.

出版信息

Zhonghua Xue Ye Xue Za Zhi. 2024 Jun 14;45(6):591-593. doi: 10.3760/cma.j.cn121090-20231128-00284.

DOI:10.3760/cma.j.cn121090-20231128-00284
PMID:39134492
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC11310815/
Abstract

Human parvovirus B19 (HPVB19) belongs to Parvoviridae, a genus of erythrovirus, and has been associated with various human diseases, and HPVB19 infection is one of the most important causes of refractory anemia after allogeneic hematopoietic stem cell transplantation (allo-HSCT). This study retrospectively analyzed 24 patients with HSCT combined with HPVB19 infection to collate and summarize the clinical presentation, treatment, and regression of patients with combined HPVB19 infection after allo-HSCT and provide experience in the management of HPVB19 infection after allo-HSCT. The median age of the patients with HPVB19 infection was 25 years, and the median time of infection occurrence was +107 days after transplantation, and 22 (91.7% ) had anemia with a median hemoglobin (HGB) level of 77.5 (46-149) g/L, and 13 (54.2% ) had new-onset anemia or persistent decline in HGB. The median length of hospital stay was 19 days. Among patients with new-onset anemia or persistent decline in HGB, the mean increase in HGB after treatment with intravenous immunoglobulin and/or antiviral therapy was 15.69 g/L, and treatment was effective in 10 (76.92% ) patients. HPVB19 infection should be alerted to the development of refractory anemia after HSCT; despite the lack of specific treatment, the overall prognosis of HPVB19-infected patients is good.

摘要

人细小病毒B19(HPVB19)属于细小病毒科,是红病毒属的一种,与多种人类疾病相关,并且HPVB19感染是异基因造血干细胞移植(allo - HSCT)后难治性贫血的最重要原因之一。本研究回顾性分析了24例allo - HSCT合并HPVB19感染的患者,以整理和总结allo - HSCT后合并HPVB19感染患者的临床表现、治疗及转归情况,为allo - HSCT后HPVB19感染的管理提供经验。HPVB19感染患者的中位年龄为25岁,感染发生的中位时间为移植后 +107天,22例(91.7%)出现贫血,血红蛋白(HGB)中位水平为77.5(46 - 149)g/L,13例(54.2%)出现新发贫血或HGB持续下降。中位住院时间为19天。在新发贫血或HGB持续下降的患者中,静脉注射免疫球蛋白和/或抗病毒治疗后HGB的平均升高值为15.69 g/L,10例(76.92%)患者治疗有效。应警惕HSCT后HPVB19感染导致难治性贫血的发生;尽管缺乏特异性治疗,但HPVB19感染患者的总体预后良好。