Clinical Tuberculosis and Epidemiology Research Center, National Research Institute of Tuberculosis and Lung Diseases (NRITLD), Shahid Beheshti University of Medical Sciences, Tehran, Iran.
Tracheal Disease Research Center, National Research Institute of Tuberculosisand Lung Diseases (NRITLD), Shahid Beheshti University of Medical Science, Tehran, Iran.
BMC Pulm Med. 2020 Oct 16;20(1):269. doi: 10.1186/s12890-020-01310-8.
Severe acute respiratory syndrome coronavirus 2 (SARS-CoV-2) that causes coronavirus disease 2019 (COVID-19) has spread to almost 100 countries, infected over 31 M patients and resulted in 961 K deaths worldwide as of 21st September 2020. The major clinical feature of severe COVID-19 requiring ventilation is acute respiratory distress syndrome (ARDS) with multi-functional failure as a result of a cytokine storm with increased serum levels of cytokines. The pathogenesis of the respiratory failure in COVID-19 is yet unknown, but diffuse alveolar damage with interstitial thickening leading to compromised gas exchange is a plausible mechanism. Hypoxia is seen in the COVID-19 patients, however, patients present with a distinct phenotype. Intracellular levels of nitric oxide (NO) play an important role in the vasodilation of small vessels. To elucidate the intracellular levels of NO inside of RBCs in COVID-19 patients compared with that of healthy control subjects.
We recruited 14 COVID-19 infected cases who had pulmonary involvement of their disease, 4 non-COVID-19 healthy controls (without pulmonary involvement and were not hypoxic) and 2 hypoxic non-COVID-19 patients subjects who presented at the Masih Daneshvari Hospital of Tehran, Iran between March-May 2020. Whole blood samples were harvested from patients and intracellular NO levels in 1 × 10 red blood cells (RBC) was measured by DAF staining using flow cytometry (FACS Calibour, BD, CA, USA).
The Mean florescent of intensity for NO was significantly enhanced in COVID-19 patients compared with healthy control subjects (P ≤ 0.05). As a further control for whether hypoxia induced this higher intracellular NO, we evaluated the levels of NO inside RBC of hypoxic patients. No significant differences in NO levels were seen between the hypoxic and non-hypoxic control group.
This pilot study demonstrates increased levels of intracellular NO in RBCs from COVID-19 patients. Future multi-centre studies should examine whether this is seen in a larger number of COVID-19 patients and whether NO therapy may be of use in these severe COVID-19 patients.
导致 2019 年冠状病毒病(COVID-19)的严重急性呼吸综合征冠状病毒 2(SARS-CoV-2)已传播到近 100 个国家,感染了超过 3100 万人,并导致截至 2020 年 9 月 21 日,全球有 96.1 万人死亡。需要通气的严重 COVID-19 的主要临床特征是急性呼吸窘迫综合征(ARDS),由于细胞因子风暴导致细胞因子血清水平升高而导致多功能衰竭。COVID-19 呼吸衰竭的发病机制尚不清楚,但是弥漫性肺泡损伤伴间质增厚导致气体交换受损是一种合理的机制。COVID-19 患者存在缺氧,但患者表现出明显的表型。细胞内一氧化氮(NO)水平在小血管扩张中起重要作用。为了阐明 COVID-19 患者与健康对照者相比,RBC 内的细胞内 NO 水平。
我们招募了 14 名患有肺部受累的 COVID-19 感染患者,4 名非 COVID-19 健康对照者(无肺部受累且不缺氧)和 2 名患有缺氧性非 COVID-19 的患者,他们于 2020 年 3 月至 5 月在伊朗德黑兰的 Masih Daneshvari 医院就诊。从患者中采集全血样本,并通过使用流式细胞术(BD,CA,USA 的 FACS Calibour)通过 DAF 染色测量 1×10 个红细胞(RBC)中的细胞内 NO 水平。
与健康对照组相比,COVID-19 患者的 NO 平均荧光强度显着增强(P≤0.05)。作为进一步控制是否缺氧诱导了这种更高的细胞内 NO,我们评估了缺氧患者 RBC 内的 NO 水平。在缺氧和非缺氧对照组之间,NO 水平没有差异。
这项初步研究表明,COVID-19 患者 RBC 中的细胞内 NO 水平升高。未来的多中心研究应检查这种情况是否在更多的 COVID-19 患者中出现,以及 NO 治疗是否对这些严重的 COVID-19 患者有用。