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多种早期因素预示着急性新冠病毒感染后会出现长期新冠症状。

Multiple early factors anticipate post-acute COVID-19 sequelae.

机构信息

Institute for Systems Biology, Seattle, WA 98109, USA; Vaccine and Infectious Disease Division, Fred Hutchinson Cancer Research Center, Seattle, WA 98109, USA; Clinical Research Division, Program in Immunology, Fred Hutchinson Cancer Research Center, Seattle, WA 98109, USA.

Institute for Systems Biology, Seattle, WA 98109, USA; Department of Bioengineering, University of Washington, Seattle, WA 98105, USA.

出版信息

Cell. 2022 Mar 3;185(5):881-895.e20. doi: 10.1016/j.cell.2022.01.014. Epub 2022 Jan 25.

Abstract

Post-acute sequelae of COVID-19 (PASC) represent an emerging global crisis. However, quantifiable risk factors for PASC and their biological associations are poorly resolved. We executed a deep multi-omic, longitudinal investigation of 309 COVID-19 patients from initial diagnosis to convalescence (2-3 months later), integrated with clinical data and patient-reported symptoms. We resolved four PASC-anticipating risk factors at the time of initial COVID-19 diagnosis: type 2 diabetes, SARS-CoV-2 RNAemia, Epstein-Barr virus viremia, and specific auto-antibodies. In patients with gastrointestinal PASC, SARS-CoV-2-specific and CMV-specific CD8 T cells exhibited unique dynamics during recovery from COVID-19. Analysis of symptom-associated immunological signatures revealed coordinated immunity polarization into four endotypes, exhibiting divergent acute severity and PASC. We find that immunological associations between PASC factors diminish over time, leading to distinct convalescent immune states. Detectability of most PASC factors at COVID-19 diagnosis emphasizes the importance of early disease measurements for understanding emergent chronic conditions and suggests PASC treatment strategies.

摘要

COVID-19 的新冠后后遗症(PASC)代表着一个新兴的全球危机。然而,PASC 的可量化风险因素及其生物学关联仍未得到很好的解决。我们对 309 名 COVID-19 患者进行了深入的多组学、纵向研究,从最初的诊断到恢复期(2-3 个月后),并与临床数据和患者报告的症状进行了整合。我们在 COVID-19 最初诊断时确定了四个预测 PASC 的风险因素:2 型糖尿病、SARS-CoV-2 RNA 血症、EB 病毒血症和特定的自身抗体。在出现胃肠道 PASC 的患者中,COVID-19 恢复期的 SARS-CoV-2 特异性和 CMV 特异性 CD8 T 细胞表现出独特的动力学。对症状相关免疫特征的分析揭示了四个终末类型的协调免疫极化,表现出不同的急性严重程度和 PASC。我们发现,PASC 因素之间的免疫关联随着时间的推移而减弱,导致不同的恢复期免疫状态。大多数 PASC 因素在 COVID-19 诊断时的可检测性强调了早期疾病测量对于理解新发慢性疾病的重要性,并提示了 PASC 的治疗策略。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/99e1/8896888/6c336441a383/fx1.jpg

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