From the Faculty of Science and Medicine, University of Fribourg, Fribourg, Switzerland.
Department of Paediatrics, Fribourg Hospital HFR, Fribourg, Switzerland.
Pediatr Infect Dis J. 2022 Feb 1;41(2):e36-e45. doi: 10.1097/INF.0000000000003413.
Although there are many hypotheses for the age-related difference in the severity of COVID-19, differences in innate, adaptive and heterologous immunity, together with differences in endothelial and clotting function, are the most likely mechanisms underlying the marked age gradient. Children have a faster and stronger innate immune response to SARS-CoV-2, especially in the nasal mucosa, which rapidly controls the virus. In contrast, adults can have an overactive, dysregulated and less effective innate response that leads to uncontrolled pro-inflammatory cytokine production and tissue injury. More recent exposure to other viruses and routine vaccines in children might be associated with protective cross-reactive antibodies and T cells against SARS-CoV-2. There is less evidence to support other mechanisms that have been proposed to explain the age-related difference in outcome following SARS-CoV-2 infection, including pre-existing immunity from exposure to common circulating coronaviruses, differences in the distribution and expression of the entry receptors ACE2 and TMPRSS2, and difference in viral load.
虽然 COVID-19 严重程度的年龄差异有许多假说,但先天免疫、适应性免疫和异源免疫的差异,以及内皮和凝血功能的差异,是导致明显年龄梯度的最可能机制。儿童对 SARS-CoV-2 具有更快、更强的先天免疫反应,尤其是在鼻腔黏膜中,可迅速控制病毒。相比之下,成年人的先天免疫反应可能过度活跃、失调且效果不佳,导致不受控制的促炎细胞因子产生和组织损伤。儿童最近接触其他病毒和常规疫苗可能与针对 SARS-CoV-2 的保护性交叉反应抗体和 T 细胞有关。对于其他已提出的解释 SARS-CoV-2 感染后与年龄相关的结果差异的机制,证据较少,包括来自常见循环冠状病毒暴露的预先存在的免疫、进入受体 ACE2 和 TMPRSS2 的分布和表达的差异,以及病毒载量的差异。