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长新冠血清学阴性患者的既往 SARS-CoV-2 感染证据。

Evidence of previous SARS-CoV-2 infection in seronegative patients with long COVID.

机构信息

Cambridge Institute of Therapeutic Immunology & Infectious Disease (CITIID), Cambridge CB2 0AW, UK; Department of Medicine, University of Cambridge, Cambridge CB2 0QQ, UK.

Cambridge Institute of Therapeutic Immunology & Infectious Disease (CITIID), Cambridge CB2 0AW, UK; Department of Medicine, University of Cambridge, Cambridge CB2 0QQ, UK; Department of Infectious Diseases, Cambridge University Hospitals NHS Foundation Trust, Cambridge CB2 0QQ, UK.

出版信息

EBioMedicine. 2022 Jul;81:104129. doi: 10.1016/j.ebiom.2022.104129. Epub 2022 Jun 27.

Abstract

BACKGROUND

There is currently no consensus on the diagnosis, definition, symptoms, or duration of COVID-19 illness. The diagnostic complexity of Long COVID is compounded in many patients who were or might have been infected with SARS-CoV-2 but not tested during the acute illness and/or are SARS-CoV-2 antibody negative.

METHODS

Given the diagnostic conundrum of Long COVID, we set out to investigate SARS-CoV-2-specific T cell responses in patients with confirmed SARS-CoV-2 infection and/or Long COVID from a cohort of mostly non-hospitalised patients.

FINDINGS

We discovered that IL-2 release (but not IFN-γ release) from T cells in response to SARS-CoV-2 peptides is both sensitive (75% +/-13%) and specific (88%+/-7%) for previous SARS-CoV-2 infection >6 months after a positive PCR test. We identified that 42-53% of patients with Long COVID, but without detectable SARS-CoV-2 antibodies, nonetheless have detectable SARS-CoV-2 specific T cell responses.

INTERPRETATION

Our study reveals evidence (detectable T cell mediated IL-2 release) of previous SARS-CoV-2 infection in seronegative patients with Long COVID.

FUNDING

This work was funded by the Addenbrooke's Charitable Trust (900276 to NS), NIHR award (G112259 to NS) and supported by the NIHR Cambridge Biomedical Research Centre. NJM is supported by the MRC (TSF MR/T032413/1) and NHSBT (WPA15-02). PJL is supported by the Wellcome Trust (PRF 210688/Z/18/Z, 084957/Z/08/Z), a Medical Research Council research grant MR/V011561/1 and the United Kingdom Research and a Innovation COVID Immunology Consortium grant (MR/V028448/1).

摘要

背景

目前对于 COVID-19 疾病的诊断、定义、症状和持续时间尚无共识。在许多急性疾病期间未接受检测和/或 SARS-CoV-2 抗体阴性的患者中,长新冠的诊断复杂性更加复杂,这些患者曾感染过 SARS-CoV-2 或可能感染过 SARS-CoV-2。

方法

鉴于长新冠的诊断难题,我们着手调查了来自大多数非住院患者队列中确诊 SARS-CoV-2 感染和/或长新冠患者的 SARS-CoV-2 特异性 T 细胞反应。

发现

我们发现,针对 SARS-CoV-2 肽的 T 细胞释放白细胞介素 2(但不释放 IFN-γ)对于 PCR 检测呈阳性后 6 个月以上的既往 SARS-CoV-2 感染具有敏感性(75% +/-13%)和特异性(88% +/-7%)。我们发现,42-53%的长新冠患者,尽管没有检测到 SARS-CoV-2 抗体,但仍有可检测到的 SARS-CoV-2 特异性 T 细胞反应。

解释

我们的研究揭示了在长新冠的血清阴性患者中存在(可检测到的 T 细胞介导的白细胞介素 2 释放)既往 SARS-CoV-2 感染的证据。

资金

这项工作得到了阿登布鲁克慈善信托基金(900276 给 NS)、NIHR 奖(G112259 给 NS)的资助,并得到了 NIHR 剑桥生物医学研究中心的支持。NJM 得到了 MRC(TSF MR/T032413/1)和 NHSBT(WPA15-02)的支持。PJL 得到了 Wellcome Trust(PRF 210688/Z/18/Z,084957/Z/08/Z)、医学研究委员会研究基金 MR/V011561/1 和英国研究与创新 COVID 免疫学联盟赠款(MR/V028448/1)的支持。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/1f1f/9253163/06e0e4e0729d/gr1.jpg

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