Petre Shotadze Tbilisi Medical Academy, Tbilisi, Georgia.
Eur Rev Med Pharmacol Sci. 2023 Dec;27(24):12134-12140. doi: 10.26355/eurrev_202312_34811.
This study aimed to better understand the link between SARS-CoV-2 infection and autoimmune rheumatic diseases (ARDs) development by analyzing blood samples from 200 registered participants, and measuring biomarkers, such as cell-free DNA, MPO (myeloperoxidase), cathepsin S, and complement type 2 receptor.
Blood samples were collected from 200 participants (100 females and 100 males; age range: 17-55 years). Participants were divided into five groups based on their COVID-19, SARS-CoV-2 nucleocapsid-specific IgG, and COVID-19 vaccination status. The Enzyme-Linked Immunosorbent Assay (ELISA) was used to identify the biomarkers.
ANOVA and t-tests revealed that the group of COVID-19 positive, SARS-CoV-2 nucleocapsid-specific IgG negative, and non-vaccinated individuals had the greatest average value for cathepsin S (p = 0.03). This suggests a correlation between the presence of COVID-19 and autoimmune disorders. The group with the greatest average value of cell-free DNA was the COVID-19-negative, SARS-CoV-2 nucleocapsid-specific IgG-negative, vaccinated group (p = 0.03). This may suggest that even though they had not contracted the disease, they may have had a stronger immune response to the virus since vaccines can stimulate an immune response even in individuals who have not been infected by the virus. Furthermore, the SARS-Cov-2 nucleocapsid-specific IgG+ and COVID-19 positive groups had higher levels of myeloperoxidase, a neutrophil protein linked to inflammation and tissue damage, suggesting a higher risk of autoimmune rheumatologic illnesses (p = 0.02).
The study suggests a correlation between COVID-19 status and the development of autoimmune disorders, as well as a potential link between a COVID-19 infection and a strong immune response. However, this study had limitations - the selection of participants and a small sample size, which offers potential for further research and examination.
通过分析 200 名注册参与者的血液样本,并测量细胞游离 DNA、髓过氧化物酶 (MPO)、组织蛋白酶 S 和补体 C2 受体等生物标志物,本研究旨在更好地了解 SARS-CoV-2 感染与自身免疫性风湿病 (ARD) 发展之间的联系。
从 200 名参与者(100 名女性和 100 名男性;年龄范围:17-55 岁)中采集血液样本。根据参与者的 COVID-19、SARS-CoV-2 核衣壳特异性 IgG 和 COVID-19 疫苗接种状态,将其分为五组。采用酶联免疫吸附试验 (ELISA) 鉴定生物标志物。
方差分析和 t 检验显示,COVID-19 阳性、SARS-CoV-2 核衣壳特异性 IgG 阴性且未接种疫苗的个体的组织蛋白酶 S 平均水平最高(p = 0.03)。这表明 COVID-19 与自身免疫性疾病之间存在相关性。细胞游离 DNA 平均水平最高的组为 COVID-19 阴性、SARS-CoV-2 核衣壳特异性 IgG 阴性、接种疫苗的组(p = 0.03)。这可能表明,即使他们没有感染该疾病,他们也可能对该病毒产生了更强的免疫反应,因为疫苗甚至可以在未感染病毒的个体中刺激免疫反应。此外,SARS-CoV-2 核衣壳特异性 IgG+和 COVID-19 阳性组的髓过氧化物酶水平较高,髓过氧化物酶是一种与炎症和组织损伤有关的中性粒细胞蛋白,这表明自身免疫性风湿病的风险较高(p = 0.02)。
该研究表明 COVID-19 状态与自身免疫性疾病的发展之间存在相关性,以及 COVID-19 感染与强烈免疫反应之间可能存在联系。然而,本研究存在一些局限性,如参与者的选择和样本量较小,这为进一步的研究和检验提供了可能性。