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在类固醇难治/依赖移植物抗宿主病的成人血液样本中通过宏基因组下一代测序揭示病毒序列。

Unmasking viral sequences by metagenomic next-generation sequencing in adult human blood samples during steroid-refractory/dependent graft-versus-host disease.

机构信息

Division of Infectious Diseases, Geneva University Hospitals, 4 Rue Gabrielle-Perret-Gentil, 1211, 14, Geneva, Switzerland.

Laboratory of Virology, Division of Laboratory Medicine, Geneva University Hospitals, 4 Rue Gabrielle-Perret-Gentil, 1211, 14, Geneva, Switzerland.

出版信息

Microbiome. 2021 Jan 24;9(1):28. doi: 10.1186/s40168-020-00953-3.

Abstract

BACKGROUND

Viral infections are common complications following allogeneic hematopoietic stem cell transplantation (allo-HSCT). Allo-HSCT recipients with steroid-refractory/dependent graft-versus-host disease (GvHD) are highly immunosuppressed and are more vulnerable to infections with weakly pathogenic or commensal viruses. Here, twenty-five adult allo-HSCT recipients from 2016 to 2019 with acute or chronic steroid-refractory/dependent GvHD were enrolled in a prospective cohort at Geneva University Hospitals. We performed metagenomics next-generation sequencing (mNGS) analysis using a validated pipeline and de novo analysis on pooled routine plasma samples collected throughout the period of intensive steroid treatment or second-line GvHD therapy to identify weakly pathogenic, commensal, and unexpected viruses.

RESULTS

Median duration of intensive immunosuppression was 5.1 months (IQR 5.5). GvHD-related mortality rate was 36%. mNGS analysis detected viral nucleotide sequences in 24/25 patients. Sequences of ≥ 3 distinct viruses were detected in 16/25 patients; Anelloviridae (24/25) and human pegivirus-1 (9/25) were the most prevalent. In 7 patients with fatal outcomes, viral sequences not assessed by routine investigations were identified with mNGS and confirmed by RT-PCR. These cases included Usutu virus (1), rubella virus (1 vaccine strain and 1 wild-type), novel human astrovirus (HAstV) MLB2 (1), classic HAstV (1), human polyomavirus 6 and 7 (2), cutavirus (1), and bufavirus (1).

CONCLUSIONS

Clinically unrecognized viral infections were identified in 28% of highly immunocompromised allo-HSCT recipients with steroid-refractory/dependent GvHD in consecutive samples. These identified viruses have all been previously described in humans, but have poorly understood clinical significance. Rubella virus identification raises the possibility of re-emergence from past infections or vaccinations, or re-infection. Video abstract.

摘要

背景

病毒感染是异基因造血干细胞移植(allo-HSCT)后的常见并发症。类固醇难治/依赖移植物抗宿主病(GvHD)的 allo-HSCT 受者免疫抑制程度高,更容易感染弱致病性或共生病毒。本研究前瞻性纳入 2016 年至 2019 年间 25 例 allo-HSCT 后发生急性或慢性类固醇难治/依赖 GvHD 的成年患者,采用经过验证的流程进行宏基因组下一代测序(mNGS)分析,并对整个强化类固醇治疗或二线 GvHD 治疗期间采集的常规血浆样本进行从头分析,以鉴定弱致病性、共生和意外病毒。

结果

中位强化免疫抑制时间为 5.1 个月(IQR 5.5)。GvHD 相关死亡率为 36%。mNGS 分析在 25 例患者中的 24 例中检测到病毒核苷酸序列。16 例患者中检测到≥3 种不同病毒的序列;细小病毒科(24/25)和人乙型肝炎病毒 1 型(9/25)最常见。在 7 例死亡病例中,通过常规检测无法评估的病毒序列通过 mNGS 检测到,并通过 RT-PCR 证实。这些病例包括乌苏图病毒(1 例)、风疹病毒(1 例疫苗株和 1 例野生型)、新型人类星状病毒 MLB2(1 例)、经典星状病毒(1 例)、人多瘤病毒 6 型和 7 型(2 例)、切割病毒(1 例)和布法病毒(1 例)。

结论

在连续样本中,28%类固醇难治/依赖 GvHD 的高度免疫抑制 allo-HSCT 受者中鉴定出临床未识别的病毒感染。这些鉴定出的病毒以前都在人类中描述过,但临床意义尚不清楚。风疹病毒的鉴定提示可能是过去感染或接种疫苗后的再次出现,或再感染。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/8679/7831233/afb92f2d7bd6/40168_2020_953_Fig1_HTML.jpg

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