Thierbach Anne, Di Cristanziano Veronica, Eberhardt Kirsten A, Pirkl Martin, Steger Gertrud, Heger Eva, Kaiser Rolf, Koch Manuel, Klein Florian, Rauschning Dominic, Malin Jakob J
Department of Anesthesiology and Intensive Care Medicine, Faculty of Medicine and University Hospital Cologne, University of Cologne, Cologne, Germany.
Institute of Virology, Faculty of Medicine and University Hospital Cologne, University of Cologne, Cologne, Germany.
J Clin Virol. 2025 Apr;177:105774. doi: 10.1016/j.jcv.2025.105774. Epub 2025 Feb 17.
Immunocompromised individuals, hemato-oncologic diseases or post-transplantation included, are, due to impaired immune response, at increased risk for severe and prolonged COVID-19. Observational Studies showed that SARS-CoV-2 RNAemia has been associated with poorer prognosis and higher disease severity.
The aim of this study was to investigate the occurrence of RNAemia and its association with anti-SARS-CoV-2 antibodies in immunocompromised COVID-19 patients. Risk factors for RNAemia were included in the analysis.
A retrospective study was conducted in 55 immunocompromised patients tested positive for SARS-CoV-2, who received treatment with monoclonal antibodies (mAb) between December 2021 and March 2022. Serological and virological tests were performed before mAb administration and clinical data were collected from electronic health records.
Out of 55 patients, 35 % showed SARS-CoV-2 RNAemia. RNAemia was present in the 2 reported fatal cases. It was associated with negative testing for anti-receptor binding domain (RBD) IgG, anti-S2 domain of spike protein (S2) IgG and a lower leukocyte count. No association was found between previous COVID-19 vaccinations and the risk for RNAemia in immunocompromised patients.
The study underscores the importance of humoral response in controlling SARS-CoV-2 replication. RNAemia can serve as a potential biomarker for disease severity in immunocompromised individuals. Therefore, it should be considered in clinical settings for appropriate therapy decisions. Further research is needed to evaluate the pathophysiology and implications of RNAemia in immunodeficient patients with COVID-19.
免疫功能低下的个体,包括血液系统肿瘤疾病患者或移植后患者,由于免疫反应受损,感染新型冠状病毒肺炎(COVID-19)后出现重症和病程延长的风险增加。观察性研究表明,严重急性呼吸综合征冠状病毒2(SARS-CoV-2)病毒血症与较差的预后和更高的疾病严重程度相关。
本研究旨在调查免疫功能低下的COVID-19患者中病毒血症的发生情况及其与抗SARS-CoV-2抗体的关系。分析病毒血症的危险因素。
对55例SARS-CoV-2检测呈阳性的免疫功能低下患者进行了一项回顾性研究,这些患者在2021年12月至2022年3月期间接受了单克隆抗体(mAb)治疗。在给予mAb之前进行了血清学和病毒学检测,并从电子健康记录中收集了临床数据。
55例患者中,35%出现SARS-CoV-2病毒血症。2例报告的死亡病例中存在病毒血症。它与抗受体结合域(RBD)IgG、刺突蛋白S2结构域(S2)IgG检测阴性以及白细胞计数较低有关。在免疫功能低下的患者中,既往COVID-19疫苗接种与病毒血症风险之间未发现关联。
该研究强调了体液反应在控制SARS-CoV-2复制中的重要性。病毒血症可作为免疫功能低下个体疾病严重程度的潜在生物标志物。因此,在临床环境中进行适当的治疗决策时应予以考虑。需要进一步研究来评估COVID-19免疫缺陷患者病毒血症的病理生理学及影响。