Stich Maximilian, Magalhães Vladimir Gonçalves, Bürger Friederike, Garbade Sven F, Jeltsch Kathrin, Mohr Kerstin, Haddad Anneke, Elling Roland, Lang Peter, Rabsteyn Armin, Jacobsen Eva-Maria, Bode Sebastian F N, Müller Barbara, Kräusslich Hans-Georg, Hoffmann Georg Friedrich, Okun Jürgen G, Bartenschlager Ralf, Binder Marco, Janda Aleš, Renk Hanna, Tönshoff Burkhard
Heidelberg University, Medical Faculty Heidelberg, Center for Pediatric and Adolescent Medicine, Department of Pediatrics I, Heidelberg, Germany.
Heidelberg University, Medical Faculty Heidelberg, Department of Infectious Diseases, Molecular Virology, Heidelberg, Germany.
J Med Virol. 2024 Dec;96(12):e70098. doi: 10.1002/jmv.70098.
The pivotal role of the cell entry receptor ACE2 for SARS-CoV-2 infection is well-established. When ACE2 is shed from cell surface into plasma as soluble ACE2 (sACE2), it can effectively neutralize SARS-CoV-2. This longitudinal prospective cohort study analyzed sACE2 activity in 1192 participants, aged 4 months to 81 years, 3 and 12 months after SARS-CoV-2 household exposure. Following SARS-CoV-2 exposure, participants exhibited significantly elevated sACE2 activity, irrespective of confirmed infection, with the highest levels observed in exposed children. Longitudinal analysis revealed a decline in sACE2 levels over time, reaching levels comparable to age- and sex-matched pre-pandemic controls. An increase in sACE2 activity was also confirmed in vitro in Calu-3 (human lung) cells within hours of SARS-CoV-2 exposure, providing a direct link between SARS-CoV-2 exposure and elevated sACE2. This study, therefore, challenges the dichotomy of categorizing SARS-CoV-2 exposed participants as infected or not infected solely on currently established diagnostic assays. It demonstrates lasting host responses independent of B- and T-cell memory and may help to keep SARS-CoV-2 infections in balance and contribute to successful virus clearance in children and adults lacking humoral and cellular immune responses following SARS-CoV-2 exposure. Trial Registration: German Registry for Clinical Studies; Identifier: D 00021521.
细胞进入受体血管紧张素转换酶2(ACE2)在严重急性呼吸综合征冠状病毒2(SARS-CoV-2)感染中的关键作用已得到充分证实。当ACE2从细胞表面脱落进入血浆成为可溶性ACE2(sACE2)时,它可以有效中和SARS-CoV-2。这项纵向前瞻性队列研究分析了1192名年龄在4个月至81岁之间的参与者在接触SARS-CoV-2家庭感染源后3个月和12个月时的sACE2活性。在接触SARS-CoV-2后,无论是否确诊感染,参与者的sACE2活性均显著升高,其中接触感染源的儿童中sACE2活性水平最高。纵向分析显示,sACE2水平随时间下降,最终达到与大流行前年龄和性别匹配的对照组相当的水平。在体外,Calu-3(人肺)细胞在接触SARS-CoV-2数小时内sACE2活性也有所增加,这直接证明了SARS-CoV-2接触与sACE2升高之间的联系。因此,这项研究对仅根据目前既定诊断检测将接触SARS-CoV-2的参与者分类为感染或未感染的二分法提出了挑战。它证明了独立于B细胞和T细胞记忆的持久宿主反应,可能有助于维持SARS-CoV-2感染的平衡,并有助于在接触SARS-CoV-2后缺乏体液和细胞免疫反应的儿童和成人中成功清除病毒。试验注册:德国临床研究注册中心;标识符:D 00021521。