Liu Li, Chen Heng-Gui, Li Ying, Li Huijun, Li Jiaoyuan, Wang Yi, Yao Shuang, Qin Chuan, Tong Shutao, Yuan Xu, Luo Xia, Miao Xiaoping, Pan An, Liu Zheng, Cheng Liming
Department of Epidemiology and Biostatistics, Ministry of Education Key Laboratory of Environment and Health, School of Public Health, Tongji Medical College, Huazhong University of Science and Technology, Wuhan 430030, China.
Department of Laboratory Medicine, Tongji Hospital, Tongji Medical College, Huazhong University of Science and Technology, Wuhan 430030, China.
Engineering (Beijing). 2021 Jul;7(7):958-965. doi: 10.1016/j.eng.2021.04.015. Epub 2021 May 18.
The longitudinal immunologic status of severe acute respiratory syndrome coronavirus 2 (SARS-CoV-2)-infected patients and its association with the clinical outcome are barely known. Thus, we sought to analyze the temporal profiles of specific antibodies, as well as the associations between the antibodies, proinflammatory cytokines, and survival of patients with coronavirus disease 2019 (COVID-19). A total of 1830 laboratory-confirmed COVID-19 cases were recruited. The temporal profiles of the virus, antibodies, and cytokines of the patients until 12 weeks since illness onset were fitted by the locally weighted scatter plot smoothing method. The mediation effect of cytokines on the associations between antibody responses and survival were explored by mediation analysis. Of the 1830 patients, 1435 were detectable for SARS-CoV-2, while 395 were positive in specific antibodies only. Of the 1435 patients, 2.4% presented seroconversion for neither immunoglobulin G (IgG) nor immunoglobulin M (IgM) during hospitalization. The seropositive rates of IgG and IgM were 29.6% and 48.1%, respectively, in the first week, and plateaued within five weeks. For the patients discharged from the hospital, the IgM decreased slowly, while high levels of IgG were maintained at around 188 AU·mL for the 12 weeks since illness onset. In contrast, in the patients who subsequently died, IgM declined rapidly and IgG dropped to 87 AU·mL at the twelfth week. Elevated interleukin-6, interleukin-8, interleukin-10, interleukin-1β, interleukin-2R, and tumor necrosis factor-α levels were observed in the deceased patients in comparison with the discharged patients, and 12.5% of the association between IgG level and mortality risk was mediated by these cytokines. Our study deciphers the temporal profiles of SARS-CoV-2-specific antibodies within the 12 weeks since illness onset and indicates the protective effect of antibody response on survival, which may help to guide prognosis estimation.
严重急性呼吸综合征冠状病毒2(SARS-CoV-2)感染患者的纵向免疫状态及其与临床结局的关联尚不清楚。因此,我们试图分析特异性抗体的时间变化情况,以及抗体、促炎细胞因子与2019冠状病毒病(COVID-19)患者生存率之间的关联。共招募了1830例实验室确诊的COVID-19病例。采用局部加权散点图平滑法拟合患者发病后12周内病毒、抗体和细胞因子的时间变化情况。通过中介分析探讨细胞因子在抗体反应与生存率之间关联中的中介作用。在1830例患者中,1435例可检测到SARS-CoV-2,而395例仅特异性抗体呈阳性。在1435例患者中,2.4%在住院期间免疫球蛋白G(IgG)和免疫球蛋白M(IgM)均未出现血清转化。IgG和IgM的血清阳性率在第一周分别为29.6%和48.1%,并在五周内趋于平稳。对于出院患者,IgM缓慢下降,而自发病后12周内IgG高水平维持在约188 AU·mL左右。相比之下,在随后死亡的患者中,IgM迅速下降,IgG在第12周降至87 AU·mL。与出院患者相比,死亡患者中白细胞介素-6、白细胞介素-8、白细胞介素-10、白细胞介素-1β、白细胞介素-2R和肿瘤坏死因子-α水平升高,这些细胞因子介导了IgG水平与死亡风险之间12.5%的关联。我们的研究解读了发病后12周内SARS-CoV-2特异性抗体的时间变化情况,并表明抗体反应对生存的保护作用,这可能有助于指导预后评估。