Ochoa-Callejero Laura, García-Sanmartín Josune, Villoslada-Blanco Pablo, Íñiguez María, Pérez-Matute Patricia, Pujadas Elisabet, Fowkes Mary E, Brody Rachel, Oteo José A, Martínez Alfredo
Oncology Area, Center for Biomedical Research of La Rioja (CIBIR), Logroño, Spain.
Infectious Diseases, Microbiota, and Metabolism Unit (CIBIR), Logroño, Spain.
J Endocr Soc. 2021 Jan 4;5(3):bvaa199. doi: 10.1210/jendso/bvaa199. eCollection 2021 Mar 1.
To better understand the biology of COVID-19, we have explored the behavior of calcitonin gene-related peptide (CGRP), an angiogenic, vasodilating, and immune modulating peptide, in severe acute respiratory syndrome coronavirus 2 positive patients.
Levels of CGRP in the serum of 57 COVID-19 patients (24 asymptomatic, 23 hospitalized in the general ward, and 10 admitted to the intensive care unit) and healthy donors (n = 24) were measured by enzyme-linked immunosorbent assay (ELISA). In addition, to better understand the physiological consequences of the observed variations, we investigated by immunofluorescence the distribution of receptor activity modifying protein 1 (RAMP1), one of the components of the CGRP receptor, in autopsy lung specimens.
CGRP levels were greatly decreased in COVID-19 patients ( < 0.001) when compared to controls, and there were no significant differences due to disease severity, sex, age, or comorbidities. We found that COVID-19 patients treated with proton pump inhibitors had lower levels of CGRP than other patients not taking this treatment ( = 0.001). RAMP1 immunoreactivity was found in smooth muscle cells of large blood vessels and the bronchial tree and in the airways´ epithelium. In COVID-19 samples, RAMP1 was also found in proliferating type II pneumocytes, a common finding in these patients.
The lower levels of CGRP should negatively impact the respiratory physiology of COVID-19 patients due to vasoconstriction, improper angiogenesis, less epithelial repair, and faulty immune response. Therefore, restoring CGRP levels in these patients may represent a novel therapeutic approach for COVID-19.
为了更好地了解新型冠状病毒肺炎(COVID-19)的生物学特性,我们研究了降钙素基因相关肽(CGRP)在严重急性呼吸综合征冠状病毒2阳性患者中的表现,CGRP是一种具有血管生成、血管舒张和免疫调节作用的肽。
采用酶联免疫吸附测定(ELISA)法检测57例COVID-19患者(24例无症状感染者、23例普通病房住院患者和10例重症监护病房患者)及健康供者(n = 24)血清中的CGRP水平。此外,为了更好地了解观察到的变化所产生的生理后果,我们通过免疫荧光法研究了CGRP受体组分之一的受体活性修饰蛋白1(RAMP1)在尸检肺标本中的分布。
与对照组相比,COVID-19患者的CGRP水平显著降低(<0.001),且在疾病严重程度、性别、年龄或合并症方面无显著差异。我们发现,接受质子泵抑制剂治疗的COVID-19患者的CGRP水平低于未接受该治疗的其他患者(=0.001)。在大血管和支气管树的平滑肌细胞以及气道上皮中发现了RAMP1免疫反应性。在COVID-19样本中,还在增殖的II型肺泡上皮细胞中发现了RAMP1,这在这些患者中很常见。
CGRP水平降低可能会因血管收缩、血管生成异常、上皮修复减少和免疫反应异常而对COVID-19患者的呼吸生理产生负面影响。因此,恢复这些患者的CGRP水平可能是一种新的COVID-19治疗方法。