Duration of infectious virus shedding of SARS-CoV-2 Omicron variant among immunocompromised patients

IF 1.5 4区 医学 Q3 INFECTIOUS DISEASES Journal of Infection and Chemotherapy Pub Date : 2025-04-01 Epub Date: 2025-01-21 DOI:10.1016/j.jiac.2025.102631
Kohei Kamegai , Naoya Itoh , Masahiro Ishikane , Noriko Iwamoto , Yusuke Asai , Nana Akazawa-Kai , Noriko Fuwa , Jin Takasaki , Masayuki Hojo , Akira Hangaishi , Tomiteru Togano , Katsuji Teruya , Kenichiro Takahashi , Sho Miyamoto , Yuichiro Hirata , Takayuki Kanno , Tomoya Saito , Harutaka Katano , Tadaki Suzuki , Norio Ohmagari
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Abstract

Objective

The duration of viral shedding and criteria for de-isolation in the hospital among immunocompromised patients with coronavirus disease 2019 (COVID-19) remain unclear. This study aimed to evaluate viral shedding duration in immunocompromised patients infected with the Omicron variant of severe acute respiratory syndrome coronavirus 2.

Methods

A prospective cohort study was performed at 2 tertiary medical centers in Japan during the Omicron epidemic waves from July 2022 to January 2023. Nasopharyngeal swabs were serially collected from immunocompromised patients with COVID-19, including those with hematological malignancies, solid tumors, autoimmune diseases, and human immunodeficiency virus infection. Patients were classified as severely or moderately immunocompromised according to the Japanese national guidelines for tixagevimab-cilgavimab. The relationship between patient characteristics, immune status, duration of viral RNA presence, and infectious virus shedding were assessed using Mann–Whitney U and Fisher's exact tests.

Results

Among 41 patients (163 samples), 9 (47 samples) were severely and 32 (116 samples) were moderately immunocompromised. In the severely and moderately immunocompromised groups, 87.2 % and 75.0 % of the samples were viral RNA-positive, while 36.2 % and 35.3 % were culture-positive, respectively. Five culture-positive samples after day 20 were from 2 severely immunocompromised patients on B cell depletion therapy. No culture-positive samples were found for the moderately immunocompromised patients after day 10.

Conclusions

Long-term viral shedding should be closely monitored in severely immunocompromised patients with COVID-19.
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免疫功能低下患者SARS-CoV-2组粒变异传染性病毒脱落的持续时间
目的:2019冠状病毒病(COVID-19)免疫功能低下患者的病毒脱落持续时间和医院去隔离标准尚不清楚。本研究旨在评估感染严重急性呼吸综合征冠状病毒2的Omicron变异免疫功能低下患者的病毒脱落时间。方法:在2022年7月至2023年1月欧米克隆流行期间,在日本2个三级医疗中心进行前瞻性队列研究。连续收集COVID-19免疫功能低下患者的鼻咽拭子,包括血液系统恶性肿瘤、实体瘤、自身免疫性疾病和人类免疫缺陷病毒感染患者。根据日本国家替沙吉维单抗-西gavimab指南,将患者分为严重或中度免疫功能低下。患者特征、免疫状态、病毒RNA存在的持续时间和传染性病毒脱落之间的关系采用Mann-Whitney U和Fisher的精确测试进行评估。结果:41例(163例)患者中,重度免疫功能低下9例(47例),中度免疫功能低下32例(116例)。在重度和中度免疫功能低下组中,病毒rna阳性的比例分别为87.2%和75.0%,培养阳性的比例分别为36.2%和35.3%。2例严重免疫功能低下患者接受B细胞耗竭治疗,20天后5例培养阳性。中度免疫功能低下患者10天后未见培养阳性样本。结论:应密切监测COVID-19严重免疫功能低下患者的长期病毒脱落情况。
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来源期刊
Journal of Infection and Chemotherapy
Journal of Infection and Chemotherapy INFECTIOUS DISEASES-PHARMACOLOGY & PHARMACY
CiteScore
4.10
自引率
4.50%
发文量
303
审稿时长
47 days
期刊介绍: The Journal of Infection and Chemotherapy (JIC) — official journal of the Japanese Society of Chemotherapy and The Japanese Association for Infectious Diseases — welcomes original papers, laboratory or clinical, as well as case reports, notes, committee reports, surveillance and guidelines from all parts of the world on all aspects of chemotherapy, covering the pathogenesis, diagnosis, treatment, and control of infection, including treatment with anticancer drugs. Experimental studies on animal models and pharmacokinetics, and reports on epidemiology and clinical trials are particularly welcome.
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