Department of Epidemiology, Bloomberg School of Public Health, Johns Hopkins University, Baltimore, Maryland.
Division of Infectious Diseases, Department of Medicine, School of Medicine, Johns Hopkins University, Baltimore, Maryland.
Transfusion. 2019 Mar;59(3):1024-1034. doi: 10.1111/trf.15140. Epub 2019 Jan 31.
Hepatitis E virus (HEV) can inapparently infect blood donors. To assess transfusion transmission of HEV in the United States, which has not been documented, a donor-recipient repository was evaluated.
To identify donations that contained HEV RNA and were linked to patient-recipients with antibody evidence of HEV exposure, we assayed samples from the Retrovirus Epidemiology Donor Study (REDS) Allogeneic Donor and Recipient repository that represents 13,201 linked donations and 3384 transfused patients. Posttransfusion samples, determined to contain IgG anti-HEV by enzyme-linked immunosorbent assay, were reassayed along with corresponding pretransfusion samples for seroconversion (incident exposure) or at least fourfold IgG anti-HEV increase (reexposure). HEV-exposed patients were linked to donations in which HEV RNA was then detected by reverse-transcription quantitative polymerase chain reaction, confirmed by transcription-mediated amplification, and phylogenetically analyzed as subgenomic cDNA sequences.
Among all patients, 19 of 1036 (1.8%) who had IgG anti-HEV before transfusion were reexposed; 40 of 2348 (1.7%) without pretransfusion IgG anti-HEV seroconverted. These 59 patients were linked to 257 donations, 1 of which was positive by reverse-transcription quantitative polymerase chain reaction and transcription-mediated amplification. Plasma from this donation contained 5.5 log IU/mL of HEV RNA that grouped with HEV genotype 3, clade 3abchij. The patient-recipient of RBCs from this donation had a greater than eightfold IgG increase; however, clinical data are unavailable.
This is the first report of probable HEV transmission via transfusion in the United States, although it has been frequently observed in Europe and Japan. Additional data on the magnitude of the risk in the United States are needed.
戊型肝炎病毒(HEV)可以无症状感染献血者。为了评估美国尚未记录的 HEV 经血传播情况,我们评估了一个献血者-受血者储存库。
为了确定含有 HEV RNA 的捐献物,并将其与具有 HEV 暴露抗体证据的患者受血者联系起来,我们检测了代表 13201 份相关捐献物和 3384 份输血患者的逆转录病毒流行病学供体研究(REDS)异基因供体和受体储存库中的样本。通过酶联免疫吸附试验确定为 IgG 抗-HEV 的输血后样本与相应的输血前样本一起重新检测,以确定是否发生血清转换(新暴露)或 IgG 抗-HEV 至少增加四倍(再暴露)。HEV 暴露的患者与随后通过逆转录定量聚合酶链反应检测到 HEV RNA 的捐献物联系起来,通过转录介导扩增进行确认,并通过亚基因组 cDNA 序列进行系统发育分析。
在所有患者中,19 例在输血前具有 IgG 抗-HEV 的患者(1.8%)再次暴露;40 例在输血前无 IgG 抗-HEV 血清转换的患者(1.7%)发生血清转换。这 59 例患者与 257 份捐献物相关,其中 1 份通过逆转录定量聚合酶链反应和转录介导扩增呈阳性。该捐献物的血浆含有 5.5 log IU/mL 的 HEV RNA,与 HEV 基因型 3、clade 3abchij 聚为一组。从该捐献物中接受 RBC 的患者的 IgG 增加了 8 倍以上;然而,临床数据不可用。
这是美国首例可能通过输血传播 HEV 的报告,尽管在欧洲和日本经常观察到这种情况。需要更多关于美国风险程度的额外数据。