Department of Developmental BioEngineering, Faculty of Science and Technology, University of Twente, Enschede, Netherlands.
Department of Medical Cell BioPhysics, Faculty of Science and Technology, University of Twente, Enschede, Netherlands.
Front Immunol. 2022 Apr 13;13:867716. doi: 10.3389/fimmu.2022.867716. eCollection 2022.
Almost 2 years from the beginning of the coronavirus disease 2019 (COVID-19) pandemic, there is still a lot unknown how the humoral response affects disease progression. In this study, we investigated humoral antibody responses against specific SARS-CoV2 proteins, their strength of binding, and their relationship with COVID severity and clinical information. Furthermore, we studied the interactions of the specific receptor-binding domain (RBD) in more depth by characterizing specific antibody response to a peptide library.
We measured specific antibodies of isotypes IgM, IgG, and IgA, as well as their binding strength against the SARS-CoV2 antigens RBD, NCP, S1, and S1S2 in sera of 76 COVID-19 patients using surface plasmon resonance imaging. In addition, these samples were analyzed using a peptide epitope mapping assay, which consists of a library of peptides originating from the RBD.
A positive association was observed between disease severity and IgG antibody titers against all SARS-CoV2 proteins and additionally for IgM and IgA antibodies directed against RBD. Interestingly, in contrast to the titer of antibodies, the binding strength went down with increasing disease severity. Within the critically ill patient group, a positive association with pulmonary embolism, d-dimer, and antibody titers was observed.
In critically ill patients, antibody production is high, but affinity is low, and maturation is impaired. This may play a role in disease exacerbation and could be valuable as a prognostic marker for predicting severity.
自 2019 年冠状病毒病(COVID-19)大流行开始以来已经过去了将近 2 年,人们仍然对体液免疫反应如何影响疾病进展知之甚少。在这项研究中,我们调查了针对特定 SARS-CoV2 蛋白的体液抗体反应、它们的结合强度以及它们与 COVID 严重程度和临床信息的关系。此外,我们通过对肽文库进行特征分析,更深入地研究了特定受体结合域(RBD)的相互作用。
我们使用表面等离子体共振成像技术测量了 76 名 COVID-19 患者血清中特定抗体同种型 IgM、IgG 和 IgA 的水平,以及它们针对 SARS-CoV2 抗原 RBD、NCP、S1 和 S1S2 的结合强度。此外,这些样本还使用肽表位作图分析进行了分析,该分析由源自 RBD 的肽文库组成。
我们观察到疾病严重程度与针对所有 SARS-CoV2 蛋白的 IgG 抗体滴度以及针对 RBD 的 IgM 和 IgA 抗体滴度呈正相关。有趣的是,与抗体滴度相反,结合强度随着疾病严重程度的增加而降低。在危重症患者组中,观察到与肺栓塞、D-二聚体和抗体滴度呈正相关。
在危重症患者中,抗体产生量高,但亲和力低,成熟受损。这可能在疾病恶化中起作用,并可作为预测严重程度的预后标志物。