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儿童中灭活疫苗诱导的 SARS-CoV-2 变异株特异性免疫。

Inactivated Vaccine-Induced SARS-CoV-2 Variant-Specific Immunity in Children.

机构信息

Millennium Institute on Immunology and Immunotherapy, Santiago, Chile.

Departamento de Genética Molecular y Microbiología, Facultad de Ciencias Biológicas, Pontificia Universidad Católica de Chile, Santiago, Chile.

出版信息

mBio. 2022 Dec 20;13(6):e0131122. doi: 10.1128/mbio.01311-22. Epub 2022 Nov 16.

Abstract

Multiple vaccines against severe acute respiratory syndrome coronavirus 2 (SARS-CoV-2) have been evaluated in clinical trials. However, trials addressing the immune response in the pediatric population are scarce. The inactivated vaccine CoronaVac has been shown to be safe and immunogenic in a phase 1/2 clinical trial in a pediatric cohort in China. Here, we report interim safety and immunogenicity results of a phase 3 clinical trial for CoronaVac in healthy children and adolescents in Chile. Participants 3 to 17 years old received two doses of CoronaVac in a 4-week interval until 31 December 2021. Local and systemic adverse reactions were registered for volunteers who received one or two doses of CoronaVac. Whole-blood samples were collected from a subgroup of 148 participants for humoral and cellular immunity analyses. The main adverse reaction reported after the first and second doses was pain at the injection site. Four weeks after the second dose, an increase in neutralizing antibody titer was observed in subjects relative to their baseline visit. Similar results were found for activation of specific CD4 T cells. Neutralizing antibodies were identified against the Delta and Omicron variants. However, these titers were lower than those for the D614G strain. Importantly, comparable CD4 T cell responses were detected against these variants of concern. Therefore, CoronaVac is safe and immunogenic in subjects 3 to 17 years old, inducing neutralizing antibody secretion and activating CD4 T cells against SARS-CoV-2 and its variants. (This study has been registered at ClinicalTrials.gov under no. NCT04992260.) This work evaluated the immune response induced by two doses of CoronaVac separated by 4 weeks in healthy children and adolescents in Chile. To date, few studies have described the effects of CoronaVac in the pediatric population. Therefore, it is essential to generate knowledge regarding the protection of vaccines in this population. Along these lines, we reported the anti-S humoral response and cellular immune response to several SARS-CoV-2 proteins that have been published and recently studied. Here, we show that a vaccination schedule consisting of two doses separated by 4 weeks induces the secretion of neutralizing antibodies against SARS-CoV-2. Furthermore, CoronaVac induces the activation of CD4 T cells upon stimulation with peptides from the proteome of SARS-CoV-2. These results indicate that, even though the neutralizing antibody response induced by vaccination decreases against the Delta and Omicron variants, the cellular response against these variants is comparable to the response against the ancestral strain D614G, even being significantly higher against Omicron.

摘要

多种针对严重急性呼吸综合征冠状病毒 2(SARS-CoV-2)的疫苗已在临床试验中进行了评估。然而,针对儿科人群免疫反应的试验却很少。在中国进行的一项 1/2 期临床试验表明,灭活疫苗科兴中维对儿童是安全且具有免疫原性的。在此,我们报告了科兴中维在智利健康儿童和青少年中进行的 3 期临床试验的中期安全性和免疫原性结果。3 至 17 岁的参与者在 2021 年 12 月 31 日之前,每 4 周接受两剂科兴中维疫苗。志愿者在接受一剂或两剂科兴中维疫苗后,会对局部和全身不良反应进行登记。对 148 名参与者中的一个亚组采集全血样本,用于体液和细胞免疫分析。与基线相比,第二剂后 4 周观察到受试者中和抗体滴度增加。对特异性 CD4 T 细胞的激活也得到了类似的结果。针对 Delta 和奥密克戎变异株均检测到中和抗体。然而,与 D614G 株相比,这些滴度较低。重要的是,针对这些关注变异株检测到了可比的 CD4 T 细胞反应。因此,科兴中维在 3 至 17 岁的受试者中是安全且具有免疫原性的,可诱导针对 SARS-CoV-2 及其变异株的中和抗体分泌和激活 CD4 T 细胞。(本研究已在 ClinicalTrials.gov 上注册,编号为 NCT04992260。)本研究评估了两剂科兴中维疫苗在智利健康儿童和青少年中每 4 周接种一次的免疫反应。迄今为止,很少有研究描述科兴中维在儿科人群中的作用。因此,必须就该人群中疫苗的保护作用生成相关知识。在此基础上,我们报告了针对已发表并最近研究的几种 SARS-CoV-2 蛋白的抗-S 体液反应和细胞免疫反应。在这里,我们表明,两剂疫苗每 4 周接种一次的方案可诱导针对 SARS-CoV-2 的中和抗体分泌。此外,科兴中维在使用 SARS-CoV-2 蛋白组的肽刺激后可诱导 CD4 T 细胞的激活。这些结果表明,尽管接种疫苗引起的中和抗体反应针对 Delta 和奥密克戎变异株有所下降,但针对这些变异株的细胞反应与针对原始株 D614G 的反应相当,甚至针对奥密克戎的反应更高。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/f194/9765711/193e46db7e92/mbio.01311-22-f001.jpg

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