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疫苗接种部位出现 SARS-CoV-2 刺突蛋白。

Emergence of SARS-CoV-2 spike protein at the vaccination site.

机构信息

Institute of Pathology, University Hospital of Ulm, Ulm, Germany.

Institute of Forensic Medicine, University Ulm, Ulm, Germany.

出版信息

Immun Inflamm Dis. 2023 Mar;11(3):e827. doi: 10.1002/iid3.827.

Abstract

BACKGROUND

The anti-coronavirus disease 2019 (COVID-19) vaccines are of paramount importance in the fight against the COVID-19 pandemic. Both viral vector- and nucleic acid-based vaccines are known to effectively induce protection against the severe acute respiratory syndrome coronavirus 2 (SARS-CoV-2) virus by generating high antibody titers and effective T-cell responses to the spike protein they encode. Although these vaccines are being applied worldwide and have been extensively investigated, the immunomorphological events at the vaccination site with respect to SARS-CoV-2 spike protein expression have not yet been described.

METHODS

We had the opportunity to examine the deltoid muscles of three men who died shortly after vaccination for unrelated reasons. We examined the vaccination sites histologically and immunohistochemically with various antibodies. Furthermore we incubated two different cell lines with one vaccine and examined the expression of the spike protein.

RESULTS

The vaccination sites show a dense lymphohistiocytic interstitial infiltrate which surrounds the small vessels and extends into the perimysium. The spike protein is expressed by histiocytic cells with a dendritic shape that are CD68-positive and CD207-negative, fibrocytes, and very rare S100-positive cells. Interestingly, the skeletal muscle, being constitutively human leukocyte antigen (HLA)-A,B,C-negative, is induced at different levels in each specimen. In a cell culture experiment, we confirmed the ability of fibroblasts and interdigitating dendritic sarcoma cells to express spike protein in vitro after incubation with the Comirnaty vaccine.

CONCLUSIONS

Histiocytic cells and fibrocytes are the heralds of spike protein synthesis at the vaccination site. The underlying cause of this apparent cell specifity is unknown. This needs to be investigated in future experiments, for example in an animal model.

摘要

背景

抗 2019 年冠状病毒病(COVID-19)疫苗对于抗击 COVID-19 大流行至关重要。已知病毒载体和核酸疫苗通过产生针对其编码的刺突蛋白的高抗体滴度和有效的 T 细胞反应,有效地诱导对严重急性呼吸综合征冠状病毒 2(SARS-CoV-2)病毒的保护。尽管这些疫苗正在全球范围内使用,并已得到广泛研究,但关于 SARS-CoV-2 刺突蛋白表达的接种部位的免疫形态学事件尚未描述。

方法

我们有机会检查了三名因与接种无关的原因而在接种后不久死亡的男性的三角肌。我们使用各种抗体对接种部位进行了组织学和免疫组织化学检查。此外,我们用一种疫苗孵育了两种不同的细胞系,并检查了刺突蛋白的表达。

结果

接种部位显示出密集的淋巴组织细胞间质浸润,围绕小血管并延伸到肌外膜。刺突蛋白由具有树突状形状的组织细胞表达,这些组织细胞呈 CD68 阳性和 CD207 阴性、成纤维细胞和非常罕见的 S100 阳性细胞。有趣的是,骨骼肌由于组成型 HLA-A、B、C 阴性,在每个标本中以不同的水平被诱导。在细胞培养实验中,我们证实了在用 Comirnaty 疫苗孵育后,成纤维细胞和交错树突状肉瘤细胞能够在体外表达刺突蛋白。

结论

组织细胞和成纤维细胞是接种部位刺突蛋白合成的先驱。这种明显的细胞特异性的潜在原因尚不清楚。这需要在未来的实验中进行研究,例如在动物模型中。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/38b2/10052447/66db29e39b91/IID3-11-e827-g002.jpg

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