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儿童重症新冠病毒病及新冠病毒感染相关儿童多系统炎症综合征中针对严重急性呼吸综合征冠状病毒2奥密克戎变异株及其他变异株的全身和下呼吸道免疫

Systemic and Lower Respiratory Tract Immunity to SARS-CoV-2 Omicron and Variants in Pediatric Severe COVID-19 and Mis-C.

作者信息

Tang Juanjie, Randolph Adrienne G, Novak Tanya, Walker Tracie C, Loftis Laura L, Zinter Matt S, Irby Katherine, Khurana Surender

机构信息

Center for Biologics Evaluation and Research (CBER), Division of Viral Products, Food and Drug Administration (FDA), Silver Spring, MD 20993, USA.

Department of Anesthesiology, Critical Care and Pain Medicine, Department of Anesthesia, Harvard Medical School, Boston Children's Hospital, Boston, MA 02115, USA.

出版信息

Vaccines (Basel). 2022 Feb 10;10(2):270. doi: 10.3390/vaccines10020270.

Abstract

Mucosal immunity plays an important role in the control of viral respiratory infections like SARS-CoV-2. While systemic immune responses against the SARS-2-CoV-2 have been studied in children, there is no information on mucosal antibody response, especially in the lower respiratory tract of children coronavirus disease 2019 (COVID-19) and post-infectious multisystem inflammatory syndrome in children (MIS-C) against emerging SARS-CoV-2 variants. Therefore, we evaluated neutralizing antibody responses in paired plasma and endotracheal aspirates of pediatric severe, acute COVID-19 or MIS-C patients against SARS-CoV-2 WA1/2020, as well as against variants of concern (VOCs). Neutralizing antibody responses against the SARS-CoV-2 WA1/2020 strain in pediatric plasma were 2-fold or 35-fold higher compared with the matched endotracheal aspirate in COVID-19 or MIS-C patients, respectively. In contrast to plasma, neutralizing antibody responses against the VOCs and variants of interest (VOIs) in endotracheal aspirates were lower, with only one endotracheal aspirate demonstrating neutralizing titers against the Iota, Kappa, Beta, Gamma, and Omicron variants. In conclusion, our findings suggest that children and adolescents with severe COVID-19 or MIS-C have weak mucosal neutralizing antibodies in the trachea against circulating SARS-CoV-2 Omicron and other VOCs, which may have implications for recovery and for re-infection with emerging SARS-CoV-2 variants.

摘要

黏膜免疫在控制如严重急性呼吸综合征冠状病毒2(SARS-CoV-2)等病毒性呼吸道感染中发挥着重要作用。虽然针对SARS-CoV-2的全身免疫反应已在儿童中进行了研究,但关于黏膜抗体反应的信息却很少,尤其是在2019冠状病毒病(COVID-19)患儿的下呼吸道以及儿童感染后多系统炎症综合征(MIS-C)中针对新出现的SARS-CoV-2变体的黏膜抗体反应。因此,我们评估了儿科重症急性COVID-19或MIS-C患者的配对血浆和气管内吸出物中针对SARS-CoV-2 WA1/2020以及关注变体(VOCs)的中和抗体反应。与COVID-19或MIS-C患者匹配的气管内吸出物相比,儿科血浆中针对SARS-CoV-2 WA1/2020毒株的中和抗体反应分别高出2倍或35倍。与血浆相反,气管内吸出物中针对VOCs和感兴趣变体(VOIs)的中和抗体反应较低,只有一份气管内吸出物显示出针对伊奥塔、卡帕、贝塔、伽马和奥密克戎变体的中和滴度。总之,我们的研究结果表明,患有重症COVID-19或MIS-C的儿童和青少年在气管中针对循环中的SARS-CoV-2奥密克戎和其他VOCs的黏膜中和抗体较弱,这可能对康复以及再次感染新出现的SARS-CoV-2变体有影响。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/3102/8879098/06daba5bf820/vaccines-10-00270-g001.jpg

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