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皮内注射奥密克戎 SARS-CoV-2 靶向 DNA 疫苗通过热驱动射流注射器给药,通过生发中心反应提供持久的中和抗体产生。

Intradermal administration of DNA vaccine targeting Omicron SARS-CoV-2 via pyro-drive jet injector provides the prolonged neutralizing antibody production via germinal center reaction.

机构信息

Department of Health Development and Medicine, Osaka University Graduate School of Medicine, Suita, Osaka, Japan.

Anges Inc., Tokyo, Japan.

出版信息

Sci Rep. 2023 Aug 10;13(1):13033. doi: 10.1038/s41598-023-40172-y.

DOI:10.1038/s41598-023-40172-y
PMID:37563266
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC10415318/
Abstract

Emerging SARS-CoV-2 Omicron variants are highly contagious with enhanced immune escape mechanisms against the initially approved COVID-19 vaccines. Therefore, we require stable alternative-platform vaccines that confer protection against newer variants of SARS-CoV-2. We designed an Omicron B.1.1.529 specific DNA vaccine using our DNA vaccine platform and evaluated the humoral and cellular immune responses. SD rats intradermally administered with Omicron-specific DNA vaccine via pyro-drive jet injector (PJI) thrice at 2-week intervals elicited high antibody titers against the Omicron subvariants as well as the ancestral strain. Indeed, the Omicron B.1.1.529-specific antibody titer and neutralizing antibody were higher than that of other strains. Longitudinal monitoring indicated that anti-spike (ancestral and Omicron) antibody titers decreased toward 30 weeks after the first vaccination dose. However, neutralization activity remained unaltered. Germinal center formation was histologically detected in lymph nodes in rats immunized with Omicron DNA vaccine. Ancestral spike-specific immune cell response was slightly weaker than Omicron spike-specific response in splenocytes with Omicron-adapted DNA vaccine, evaluated by ELISpot assay. Collectively, our findings suggest that Omicron targeting DNA vaccines via PJI can elicit robust durable antibody production mediated by germinal center reaction against this new variant as well as partially against the spike protein of other SARS-CoV-2 variants.

摘要

新出现的 SARS-CoV-2 奥密克戎变体具有高度传染性,并对最初批准的 COVID-19 疫苗具有增强的免疫逃逸机制。因此,我们需要稳定的替代平台疫苗,以提供针对 SARS-CoV-2 新型变体的保护。我们使用 DNA 疫苗平台设计了一种针对奥密克戎 B.1.1.529 的特异性 DNA 疫苗,并评估了其体液和细胞免疫反应。通过皮内注射(PJI)将奥密克戎特异性 DNA 疫苗三次皮内给药,间隔 2 周,SD 大鼠可产生针对奥密克戎亚变体和原始株的高抗体滴度。实际上,奥密克戎 B.1.1.529 特异性抗体滴度和中和抗体滴度均高于其他菌株。纵向监测表明,接种第一剂疫苗 30 周后,抗刺突(原始和奥密克戎)抗体滴度下降。然而,中和活性保持不变。在接种奥密克戎 DNA 疫苗的大鼠淋巴结中,通过组织学检测到生发中心形成。通过 ELISpot 测定,用奥密克戎适应的 DNA 疫苗评估脾细胞中的祖先刺突特异性免疫细胞反应,发现其比奥密克戎刺突特异性反应略弱。总的来说,我们的研究结果表明,通过 PJI 接种奥密克戎靶向 DNA 疫苗可以引发针对这种新型变体以及其他 SARS-CoV-2 变体的刺突蛋白的持久、持久的抗体产生,这是由生发中心反应介导的。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/df9c/10415318/717f9ec918ad/41598_2023_40172_Fig4_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/df9c/10415318/bcae9edce5e0/41598_2023_40172_Fig1_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/df9c/10415318/495912d5b33f/41598_2023_40172_Fig2_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/df9c/10415318/554bbe872c27/41598_2023_40172_Fig3_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/df9c/10415318/717f9ec918ad/41598_2023_40172_Fig4_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/df9c/10415318/bcae9edce5e0/41598_2023_40172_Fig1_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/df9c/10415318/495912d5b33f/41598_2023_40172_Fig2_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/df9c/10415318/554bbe872c27/41598_2023_40172_Fig3_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/df9c/10415318/717f9ec918ad/41598_2023_40172_Fig4_HTML.jpg

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