Swiss Institute of Allergy and Asthma Research (SIAF), University of Zurich, Davos, Switzerland.
Christine Kühne - Center for Research and Education (CK-CARE), Davos, Switzerland.
Allergy. 2020 Nov;75(11):2829-2845. doi: 10.1111/all.14429. Epub 2020 Aug 24.
Morbidity and mortality from COVID-19 caused by novel coronavirus SARS-CoV-2 is accelerating worldwide, and novel clinical presentations of COVID-19 are often reported. The range of human cells and tissues targeted by SARS-CoV-2, its potential receptors and associated regulating factors are still largely unknown. The aim of our study was to analyze the expression of known and potential SARS-CoV-2 receptors and related molecules in the extensive collection of primary human cells and tissues from healthy subjects of different age and from patients with risk factors and known comorbidities of COVID-19.
We performed RNA sequencing and explored available RNA-Seq databases to study gene expression and co-expression of ACE2, CD147 (BSG), and CD26 (DPP4) and their direct and indirect molecular partners in primary human bronchial epithelial cells, bronchial and skin biopsies, bronchoalveolar lavage fluid, whole blood, peripheral blood mononuclear cells (PBMCs), monocytes, neutrophils, DCs, NK cells, ILC1, ILC2, ILC3, CD4 and CD8 T cells, B cells, and plasmablasts. We analyzed the material from healthy children and adults, and from adults in relation to their disease or COVID-19 risk factor status.
ACE2 and TMPRSS2 were coexpressed at the epithelial sites of the lung and skin, whereas CD147 (BSG), cyclophilins (PPIA andPPIB), CD26 (DPP4), and related molecules were expressed in both epithelium and in immune cells. We also observed a distinct age-related expression profile of these genes in the PBMCs and T cells from healthy children and adults. Asthma, COPD, hypertension, smoking, obesity, and male gender status generally led to the higher expression of ACE2- and CD147-related genes in the bronchial biopsy, BAL, or blood. Additionally, CD147-related genes correlated positively with age and BMI. Interestingly, we also observed higher expression of CD147-related genes in the lesional skin of patients with atopic dermatitis.
Our data suggest different receptor repertoire potentially involved in the SARS-CoV-2 infection at the epithelial barriers and in the immune cells. Altered expression of these receptors related to age, gender, obesity and smoking, as well as with the disease status, might contribute to COVID-19 morbidity and severity patterns.
由新型冠状病毒 SARS-CoV-2 引起的 COVID-19 的发病率和死亡率正在全球范围内加速上升,并且经常报道 COVID-19 的新的临床表现。SARS-CoV-2 靶向的人体细胞和组织范围、其潜在受体以及相关调节因子在很大程度上仍然未知。我们研究的目的是分析来自不同年龄的健康受试者和具有 COVID-19 风险因素和已知合并症的患者的大量原发性人细胞和组织中已知和潜在的 SARS-CoV-2 受体及其相关分子的表达。
我们进行了 RNA 测序并探索了可用的 RNA-Seq 数据库,以研究原发性人支气管上皮细胞、支气管和皮肤活检、支气管肺泡灌洗液、全血、外周血单核细胞 (PBMC)、单核细胞、嗜中性粒细胞、DC、NK 细胞、ILC1、ILC2、ILC3、CD4 和 CD8 T 细胞、B 细胞和浆母细胞中 ACE2、CD147(BSG)和 CD26(DPP4)及其直接和间接分子伴侣的基因表达和共表达。我们分析了来自健康儿童和成人以及与疾病或 COVID-19 风险因素有关的成人的材料。
ACE2 和 TMPRSS2 在肺和皮肤的上皮部位共同表达,而 CD147(BSG)、亲环素(PPIA 和 PPIB)、CD26(DPP4)和相关分子在上皮细胞和免疫细胞中表达。我们还观察到健康儿童和成人 PBMC 和 T 细胞中这些基因的年龄相关表达谱。哮喘、COPD、高血压、吸烟、肥胖和男性性别状况通常导致支气管活检、BAL 或血液中 ACE2 和 CD147 相关基因的表达更高。此外,CD147 相关基因与年龄和 BMI 呈正相关。有趣的是,我们还观察到特应性皮炎患者皮损皮肤中 CD147 相关基因的表达更高。
我们的数据表明,在上皮屏障和免疫细胞中,SARS-CoV-2 感染可能涉及不同的受体谱。这些受体与年龄、性别、肥胖和吸烟以及疾病状态相关的表达改变可能导致 COVID-19 的发病率和严重程度模式。