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接种疫苗和感染 SARS-CoV-2 的儿童的黏膜免疫反应的比较。

SARS-CoV-2-specific mucosal immune response in vaccinated versus infected children.

机构信息

Department of Maternal, Child Health and Urological Sciences, Sapienza University of Rome, Rome, Italy.

B Cell Unit, Immunology Research Area, Bambino Gesù Children's Hospital, Istituti di Ricovero e Cura a Carattere Scientifico (IRCCS), Rome, Italy.

出版信息

Front Cell Infect Microbiol. 2024 Mar 27;14:1231697. doi: 10.3389/fcimb.2024.1231697. eCollection 2024.

Abstract

The anti-COVID-19 intramuscular vaccination induces a strong systemic but a weak mucosal immune response in adults. Little is known about the mucosal immune response in children infected or vaccinated against SARS-CoV-2. We found that 28% of children had detectable salivary IgA against SARS-CoV-2 even before vaccination, suggesting that, in children, SARS-CoV-2 infection may be undiagnosed. After vaccination, only receptor-binding domain (RBD)-specific IgA1 significantly increased in the saliva. Conversely, infected children had significantly higher salivary RBD-IgA2 compared to IgA1, indicating that infection more than vaccination induces a specific mucosal immune response in children. Future efforts should focus on development of vaccine technologies that also activate mucosal immunity.

摘要

抗 COVID-19 肌肉内疫苗接种可在成年人中引起强烈的全身免疫反应,但粘膜免疫反应较弱。对于感染或接种 SARS-CoV-2 疫苗的儿童的粘膜免疫反应知之甚少。我们发现,即使在接种疫苗之前,仍有 28%的儿童的唾液中可检测到针对 SARS-CoV-2 的 IgA,这表明儿童中的 SARS-CoV-2 感染可能未被诊断。接种疫苗后,唾液中仅受体结合域(RBD)特异性 IgA1 显著增加。相反,感染 SARS-CoV-2 的儿童的唾液 RBD-IgA2 明显高于 IgA1,表明感染比接种疫苗更能诱导儿童的特异性粘膜免疫反应。未来的研究应集中于开发可同时激活粘膜免疫的疫苗技术。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/b938/11004290/d39d2651fd80/fcimb-14-1231697-g001.jpg

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