Protease inhibitor plasma concentrations associate with COVID-19 infection.

Oxford open immunology Pub Date : 2021-07-07 eCollection Date: 2021-01-01 DOI:10.1093/oxfimm/iqab014
Nicholas R Medjeral-Thomas, Anne Troldborg, Annette G Hansen, Rasmus Pihl, Candice L Clarke, James E Peters, David C Thomas, Michelle Willicombe, Yaseelan Palarasah, Marina Botto, Matthew C Pickering, Steffen Thiel
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Abstract

Protease inhibitors influence a range of innate immunity and inflammatory pathways. We quantified plasma concentrations of key anti-inflammatory protease inhibitors in chronic haemodialysis patients with coronavirus disease 2019 (COVID-19). The samples were collected early in the disease course to determine whether plasma protease inhibitor levels associated with the presence and severity of COVID-19. We used antibody-based immunoassays to measure plasma concentrations of C1 esterase inhibitor, alpha2-macroglobulin, antithrombin and inter-alpha-inhibitor heavy chain 4 (ITIH4) in 100 serial samples from 27 haemodialysis patients with COVID-19. ITIH4 was tested in two assays, one measuring intact ITIH4 and another also detecting any fragmented ITIH4 (total ITIH4). Control cohorts were 32 haemodialysis patients without COVID-19 and 32 healthy controls. We compared protease inhibitor concentration based on current and future COVID-19 severity and with C-reactive protein. Results were adjusted for repeated measures and multiple comparisons. Analysis of all available samples demonstrated lower plasma C1 esterase inhibitor and α2M and higher total ITIH4 in COVID-19 compared with dialysis controls. These differences were also seen in the first sample collected after COVID-19 diagnosis, a median of 4 days from diagnostic swab. Plasma ITIH4 levels were higher in severe than the non-severe COVID-19. Serum C-reactive protein correlated positively with plasma levels of antithrombin, intact ITIH4 and total ITIH4. In conclusion, plasma protease inhibitor concentrations are altered in COVID-19.

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蛋白酶抑制剂血浆浓度与新冠肺炎感染相关。
蛋白酶抑制剂影响一系列先天免疫和炎症途径。我们量化了2019冠状病毒病(新冠肺炎)慢性血液透析患者中关键抗炎蛋白酶抑制剂的血浆浓度。在病程早期采集样本,以确定血浆蛋白酶抑制剂水平是否与新冠肺炎的存在和严重程度相关。我们使用基于抗体的免疫测定法测量了27名新冠肺炎血液透析患者的100份系列样本中C1酯酶抑制剂、α2-巨球蛋白、抗凝血酶和α间抑制剂重链4(ITIH4)的血浆浓度。ITIH4在两种测定中进行了测试,一种测定完整的ITIH4,另一种也检测任何片段的ITIH4(总ITIH4)。对照组为32名无新冠肺炎的血液透析患者和32名健康对照组。我们比较了基于当前和未来新冠肺炎严重程度的蛋白酶抑制剂浓度以及C反应蛋白。对重复测量和多次比较的结果进行了调整。对所有可用样本的分析表明,与透析对照组相比,新冠肺炎患者的血浆C1酯酶抑制剂和α2M较低,总ITIH4较高。这些差异也出现在新冠肺炎诊断后采集的第一份样本中,诊断拭子平均4天。重症患者的血浆ITIH4水平高于非重症新冠肺炎患者。血清C反应蛋白与血浆抗凝血酶、完整ITIH4和总ITIH4水平呈正相关。总之,血浆蛋白酶抑制剂浓度在新冠肺炎中发生改变。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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CiteScore
2.20
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审稿时长
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