Departamento de Patologia (LIM 05), Faculdade de Medicina da Universidade de São Paulo, São Paulo, Brazil.
Laboratório de Investigação Médica (LIM03), Faculdade de Medicina, Hospital das Clínicas HCFMUSP, Universidade de São Paulo, São Paulo, Brazil.
Respir Res. 2023 Nov 14;24(1):281. doi: 10.1186/s12931-023-02555-7.
Lung fibrosis is a major concern in severe COVID-19 patients undergoing mechanical ventilation (MV). Lung fibrosis frequency in post-COVID syndrome is highly variable and even if the risk is proportionally small, many patients could be affected. However, there is still no data on lung extracellular matrix (ECM) composition in severe COVID-19 and whether it is different from other aetiologies of ARDS.
We have quantified different ECM elements and TGF-β expression in lung tissue of 28 fatal COVID-19 cases and compared to 27 patients that died of other causes of ARDS, divided according to MV duration (up to six days or seven days or more). In COVID-19 cases, ECM elements were correlated with lung transcriptomics and cytokines profile.
We observed that COVID-19 cases presented significant increased deposition of collagen, fibronectin, versican, and TGF-β, and decreased decorin density when compared to non-COVID-19 cases of similar MV duration. TGF-β was precociously increased in COVID-19 patients with MV duration up to six days. Lung collagen was higher in women with COVID-19, with a transition of upregulated genes related to fibrillogenesis to collagen production and ECM disassembly along the MV course.
Fatal COVID-19 is associated with an early TGF-β expression lung environment after the MV onset, followed by a disordered ECM assembly. This uncontrolled process resulted in a prominent collagen deposition when compared to other causes of ARDS. Our data provides pathological substrates to better understand the high prevalence of pulmonary abnormalities in patients surviving COVID-19.
肺纤维化是重症 COVID-19 患者接受机械通气(MV)的主要关注点。新冠后综合征中的肺纤维化频率变化很大,即使风险成比例较小,也会有许多患者受到影响。然而,目前关于严重 COVID-19 患者肺细胞外基质(ECM)组成以及其是否与其他 ARDS 病因不同的数据仍缺乏。
我们定量检测了 28 例致命性 COVID-19 病例和 27 例因其他原因导致 ARDS 而死亡的患者的肺组织中不同的 ECM 成分和 TGF-β表达,并根据 MV 持续时间(6 天或 7 天或更长)进行了比较。在 COVID-19 病例中,ECM 成分与肺转录组学和细胞因子谱相关。
与 MV 持续时间相似的非 COVID-19 病例相比,我们观察到 COVID-19 病例的胶原蛋白、纤维连接蛋白、软骨素聚糖和 TGF-β沉积显著增加,而decorin 密度降低。在 MV 持续时间达 6 天的 COVID-19 患者中,TGF-β 提前增加。在 COVID-19 女性患者中,肺胶原蛋白含量更高,与纤维形成相关的上调基因向胶原蛋白生成和 ECM 解体的转变伴随着 MV 过程。
致命性 COVID-19 与 MV 发病后早期 TGF-β表达的肺环境有关,随后 ECM 组装失调。与其他 ARDS 病因相比,这一失控过程导致了明显的胶原蛋白沉积。我们的数据为更好地理解 COVID-19 幸存者中肺异常的高发生率提供了病理基础。