Service d'Hématologie Clinique, Centre Hospitalier Universitaire de Nice, Nice, France.
Université de Paris, Inserm U976, Insight team, F-75010, Paris France Unité Virologie et greffes, Département des agents infectieux, Hôpital Saint-Louis, APHP, Paris, France.
Transpl Infect Dis. 2023 Oct;25(5):e14118. doi: 10.1111/tid.14118. Epub 2023 Aug 18.
Human parvovirus B19 (B19V) infection is associated with pure red cell aplasia (PRCA) in immunocompromised patients; however, the spectrum of manifestations associated with B19V in allogeneic hematopoietic stem cell transplantation recipients (alloHSCT) has rarely been reported.
In this study, we aimed to report clinical and immune features of B19V infection after alloHSCT. We retrospectively collected and analyzed clinical and microbiological data of all transplanted patients with B19V DNAmia or tissue infection detected by polymerase chain reaction (PCR) in our center from 2010 to 2021.
We report 35 cases of B19V infections in 33 patients. Median time from transplant to B19V first PCR positivity was 6.9 months (interquartile range (IQR) [1.6-18.9]). No preferential immune profile, type of transplantation or conditioning was identified. Hematological impairment was the most frequent sign, followed by rash and fever. Unconventional clinical forms were also detected, such as acute myelitis and myositis. For some cases, the direct relationship between symptoms and B19V infection was difficult to prove but was suggested by targeted tissue PCR positivity. When hematological impairment was not at the forefront, reticulocytopenia helped to diagnose B19V infections. Treatment was mainly based on high dose intravenous immunoglobulin.
Although hematological impairment was the most frequent sign, B19V can affect multiple targets and lead to atypical manifestations. Because of its heterogeneous clinical presentation, B19V infection is likely under-diagnosed. Diagnosis of unusual B19V organ involvement needs combination of arguments which can include targeted tissue PCR.
人类细小病毒 B19(B19V)感染与免疫功能低下患者的纯红细胞再生障碍性贫血(PRCA)有关;然而,异体造血干细胞移植受者(alloHSCT)中与 B19V 相关的表现谱很少有报道。
在本研究中,我们旨在报告 alloHSCT 后 B19V 感染的临床和免疫特征。我们回顾性地收集并分析了 2010 年至 2021 年在我们中心通过聚合酶链反应(PCR)检测到 B19V DNAemia 或组织感染的所有移植患者的临床和微生物学数据。
我们报告了 33 名患者中的 35 例 B19V 感染。从移植到 B19V 首次 PCR 阳性的中位时间为 6.9 个月(四分位距(IQR)[1.6-18.9])。未发现优先免疫谱、移植类型或预处理方式。血液学损害是最常见的表现,其次是皮疹和发热。还检测到非传统的临床形式,如急性脊髓炎和肌炎。对于一些病例,症状与 B19V 感染之间的直接关系难以证明,但组织 PCR 阳性提示存在这种关系。当血液学损害不是主要表现时,网织红细胞减少有助于诊断 B19V 感染。治疗主要基于大剂量静脉注射免疫球蛋白。
尽管血液学损害是最常见的表现,但 B19V 可影响多个靶器官并导致非典型表现。由于其临床表现的异质性,B19V 感染可能被低估。诊断不常见的 B19V 器官受累需要结合论据,包括靶向组织 PCR。