School of Life Sciences, University of Nottingham, Nottingham, UK.
School of Medicine, Cardiff University, Cardiff, UK.
J Clin Immunol. 2024 Jun 10;44(6):147. doi: 10.1007/s10875-024-01739-0.
Asymptomatic SARS-CoV-2 infections were widely reported during the COVID-19 pandemic, acting as a hidden source of infection. Many existing studies investigating asymptomatic immunity failed to recruit true asymptomatic individuals. Thus, we conducted a longitudinal cohort study to evaluate humoral- and cell-mediated responses to infection and vaccination in well-defined asymptomatic young adults (the Asymptomatic COVID-19 in Education [ACE] cohort).
Asymptomatic testing services located at three UK universities identified asymptomatic young adults who were subsequently recruited with age- and sex-matched symptomatic and uninfected controls. Blood and saliva samples were collected after SARS-CoV-2 Wuhan infection, and again after vaccination. 51 participant's anti-spike antibody titres, neutralizing antibodies, and spike-specific T-cell responses were measured, against both Wuhan and Omicron B.1.1.529.1.
Asymptomatic participants exhibited reduced Wuhan-specific neutralization antibodies pre- and post-vaccination, as well as fewer Omicron-specific neutralization antibodies post-vaccination, compared to symptomatic participants. Lower Wuhan and Omicron-specific IgG titres in asymptomatic individuals were also observed pre- and post-vaccination, compared to symptomatic participants. There were no differences in salivary IgA levels. Conventional flow cytometry analysis and multi-dimensional clustering analysis indicated unvaccinated asymptomatic participants had significantly fewer Wuhan-specific IL-2 secreting CD4 CD45RA T cells and activated CD8 T cells than symptomatic participants, though these differences dissipated after vaccination.
Asymptomatic infection results in decreased antibody and T cell responses to further exposure to SARS-CoV-2 variants, compared to symptomatic infection. Post-vaccination, antibody responses are still inferior, but T cell immunity increases to match symptomatic subjects, emphasising the importance of vaccination to help protect asymptomatic individuals against future variants.
在 COVID-19 大流行期间,广泛报道了无症状 SARS-CoV-2 感染,成为感染的隐性来源。许多现有的研究调查无症状免疫的研究未能招募到真正的无症状个体。因此,我们进行了一项纵向队列研究,以评估明确的无症状年轻成年人(无症状 COVID-19 在教育中的研究 [ACE] 队列)对感染和疫苗接种的体液和细胞介导的反应。
位于英国三所大学的无症状检测服务机构确定了无症状的年轻人,随后招募了年龄和性别匹配的有症状和未感染的对照组。在 SARS-CoV-2 武汉感染后,以及再次接种疫苗后,采集血液和唾液样本。测量了 51 名参与者的抗刺突抗体滴度、中和抗体和针对武汉和奥密克戎 B.1.1.529.1 的刺突特异性 T 细胞反应。
与有症状的参与者相比,无症状参与者在接种疫苗前后的武汉特异性中和抗体减少,以及接种疫苗后的奥密克戎特异性中和抗体减少。与有症状的参与者相比,无症状个体在接种疫苗前后的武汉和奥密克戎特异性 IgG 滴度也较低。唾液 IgA 水平没有差异。常规流式细胞术分析和多维聚类分析表明,未接种疫苗的无症状参与者比有症状的参与者产生的武汉特异性 IL-2 分泌 CD4 CD45RA T 细胞和激活的 CD8 T 细胞显著减少,但这些差异在接种疫苗后消失。
与有症状的感染相比,无症状感染导致对 SARS-CoV-2 变体进一步暴露的抗体和 T 细胞反应降低。接种疫苗后,抗体反应仍然较差,但 T 细胞免疫增加到与有症状的个体相匹配,强调了接种疫苗对帮助保护无症状个体免受未来变体的重要性。