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在进展为长新冠的患者中,出现自发、持续、依赖 T 细胞的 IFN-γ 释放。

Spontaneous, persistent, T cell-dependent IFN-γ release in patients who progress to Long Covid.

机构信息

Cambridge Institute of Therapeutic Immunology and Infectious Disease (CITIID), Cambridge CB2 0AW, UK.

Department of Medicine, University of Cambridge, Cambridge CB2 0QQ, UK.

出版信息

Sci Adv. 2024 Feb 23;10(8):eadi9379. doi: 10.1126/sciadv.adi9379. Epub 2024 Feb 21.

Abstract

After acute infection with severe acute respiratory syndrome coronavirus-2 (SARS-CoV-2), a proportion of patients experience persistent symptoms beyond 12 weeks, termed Long Covid. Understanding the mechanisms that cause this debilitating disease and identifying biomarkers for diagnostic, therapeutic, and monitoring purposes are urgently required. We detected persistently high levels of interferon-γ (IFN-γ) from peripheral blood mononuclear cells of patients with Long Covid using highly sensitive FluoroSpot assays. This IFN-γ release was seen in the absence of ex vivo peptide stimulation and remains persistently elevated in patients with Long Covid, unlike the resolution seen in patients recovering from acute SARS-CoV-2 infection. The IFN-γ release was CD8 T cell-mediated and dependent on antigen presentation by CD14 cells. Longitudinal follow-up of our study cohort showed that symptom improvement and resolution correlated with a decrease in IFN-γ production to baseline levels. Our study highlights a potential mechanism underlying Long Covid, enabling the search for biomarkers and therapeutics in patients with Long Covid.

摘要

在严重急性呼吸综合征冠状病毒 2(SARS-CoV-2)急性感染后,一部分患者出现持续 12 周以上的症状,称为长新冠。了解导致这种使人衰弱的疾病的机制,并确定用于诊断、治疗和监测目的的生物标志物,这是迫切需要的。我们使用高度敏感的 FluoroSpot 检测法,从长新冠患者的外周血单核细胞中检测到持续高水平的干扰素-γ(IFN-γ)。这种 IFN-γ 释放是在没有体外肽刺激的情况下发生的,并且在长新冠患者中持续升高,与急性 SARS-CoV-2 感染后患者的缓解情况不同。IFN-γ 的释放是由 CD8 T 细胞介导的,并且依赖于 CD14 细胞的抗原呈递。对我们研究队列的纵向随访表明,症状的改善和缓解与 IFN-γ 产生降至基线水平相关。我们的研究强调了长新冠的潜在机制,为长新冠患者寻找生物标志物和治疗方法提供了可能。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/2ec6/10881041/6116747f2672/sciadv.adi9379-f1.jpg

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