Fang Jia-Long, Shrestha Leeza, Beland Frederick A
Division of Biochemical Toxicology, National Center for Toxicological Research, U.S. Food and Drug Administration, Jefferson, AR, 72079, USA.
Sci Rep. 2025 Mar 25;15(1):10300. doi: 10.1038/s41598-025-92389-8.
COVID-19 is an infectious disease caused by the severe acute respiratory syndrome coronavirus (SARS-CoV-2). Anti-SARS-CoV-2 antibodies can provide information on patient immunity, identify asymptomatic patients, and track the spread of COVID-19. Efforts have been made to develop methods to detect anti-SARS-CoV-2 antibodies in humans. Here, we describe a flow cytometric assay for the simultaneous detection of anti-SARS-CoV-2 IgG and IgM in human plasma. To assess the antibody response against the different SARS-CoV-2 structural proteins, five viral recombinant proteins, including spike protein subunit 1 (S1), N-terminal domain of S1 (S1A), spike receptor-binding domain (RBD), spike protein subunit 2 (S2), and nucleocapsid protein (N), were generated. A comparison of the antibody profiles detected by the assay with plasma from 100 healthy blood donors collected prior to the COVID-19 pandemic and plasma from 100 virologically confirmed COVID-19 patients demonstrated a clear discrimination between the two groups. Among the COVID-19 patients, the antibody responses for the viral proteins, as determined by their prevalence, were anti-RBD IgG = anti-N IgG > anti-S1 IgG > anti-S1A IgG > anti-S2 IgG, and anti-RBD IgM > anti-S1 IgM > anti-N IgM > anti-S2 IgM. The prevalence of anti-SARS-CoV-2 IgG and IgM was not associated with sex, age, race, days after the onset of symptoms, or severity of illness, except for a higher prevalence of anti-S2 IgG being observed in men than in women. The levels of anti-RBD IgG were higher in patients 65 years and older and in patients who had severe symptoms. Similarly, patients who had severe symptoms exhibited higher levels of anti-S1 and anti-S1A IgG than patients who had mild or moderate symptoms. The levels of anti-RBD IgM tended to be higher in men but did not differ among age, race, days after the onset of symptoms, or severity of illness. Our study indicates that the flow cytometric assay, especially using RBD as target antigen, can be used to detect simultaneously anti-SARS-CoV-2 IgG and IgM antibodies in human plasma.
新型冠状病毒肺炎(COVID-19)是一种由严重急性呼吸综合征冠状病毒2(SARS-CoV-2)引起的传染病。抗SARS-CoV-2抗体可提供有关患者免疫力的信息,识别无症状患者,并追踪COVID-19的传播情况。人们已努力开发检测人类抗SARS-CoV-2抗体的方法。在此,我们描述了一种流式细胞术检测方法,用于同时检测人血浆中的抗SARS-CoV-2 IgG和IgM。为了评估针对不同SARS-CoV-2结构蛋白的抗体反应,制备了五种病毒重组蛋白,包括刺突蛋白亚基1(S1)、S1的N端结构域(S1A)、刺突受体结合结构域(RBD)、刺突蛋白亚基2(S2)和核衣壳蛋白(N)。将该检测方法检测到的抗体谱与100名在COVID-19大流行之前采集的健康献血者的血浆以及100名经病毒学确诊的COVID-19患者的血浆进行比较,结果显示两组之间有明显区别。在COVID-19患者中,根据病毒蛋白的流行率确定的抗体反应为:抗RBD IgG = 抗N IgG > 抗S1 IgG > 抗S1A IgG > 抗S2 IgG,以及抗RBD IgM > 抗S1 IgM > 抗N IgM > 抗S2 IgM。抗SARS-CoV-2 IgG和IgM的流行率与性别、年龄、种族、症状出现后天数或疾病严重程度无关,但观察到男性中抗S2 IgG的流行率高于女性。65岁及以上患者和有严重症状的患者中抗RBD IgG水平较高。同样,有严重症状的患者比有轻度或中度症状的患者表现出更高水平的抗S1和抗S1A IgG。抗RBD IgM水平在男性中往往较高,但在年龄、种族、症状出现后天数或疾病严重程度方面没有差异。我们的研究表明,流式细胞术检测方法,尤其是以RBD作为靶抗原,可用于同时检测人血浆中的抗SARS-CoV-2 IgG和IgM抗体。