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BNT162b2疫苗接种1年后儿童中检测到非炎性严重急性呼吸综合征冠状病毒2刺突特异性IgG4抗体的延迟诱导。

Delayed Induction of Noninflammatory SARS-CoV-2 Spike-Specific IgG4 Antibodies Detected 1 Year After BNT162b2 Vaccination in Children.

作者信息

Kobbe Robin, Rau Cornelius, Schulze-Sturm Ulf, Stahl Felix, Fonseca-Brito Luis, Diemert Anke, Lütgehetmann Marc, Addo Marylyn M, Arck Petra, Weskamm Leonie M

机构信息

From the Institute for Infection Research and Vaccine Development.

Department of Infectious Disease Epidemiology.

出版信息

Pediatr Infect Dis J. 2024 Jul 30;43(12):1200-3. doi: 10.1097/INF.0000000000004488.

DOI:10.1097/INF.0000000000004488
PMID:39078156
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC11542969/
Abstract

Humoral immune responses after BNT162b2 vaccination are predominantly composed of immunoglobulin (Ig) G1 and IgG3 subclass antibodies. As previously described in adults, S1-specific and receptor-binding domain-specific IgG4 levels increase significantly 1 year after the second BNT162b2 vaccination in children 5-11 years of age. Understanding mRNA vaccine-specific IgG4 responses in all age groups is crucial as more mRNA vaccines will reach licensure in the coming years.

摘要

BNT162b2疫苗接种后的体液免疫反应主要由免疫球蛋白(Ig)G1和IgG3亚类抗体组成。如先前在成人中所描述的,在5至11岁儿童中,第二次接种BNT162b2疫苗1年后,S1特异性和受体结合域特异性IgG4水平显著升高。随着未来几年更多的mRNA疫苗获得许可,了解所有年龄组中mRNA疫苗特异性IgG4反应至关重要。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/8857/11542969/f5fef7b9f61e/inf-43-1200-g001.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/8857/11542969/f5fef7b9f61e/inf-43-1200-g001.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/8857/11542969/f5fef7b9f61e/inf-43-1200-g001.jpg

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