科研成果详情

题名Nucleocapsid protein of SARS-CoV-2 is a potential target for developing new generation of vaccine
作者
发表日期2022-06
发表期刊JOURNAL OF CLINICAL LABORATORY ANALYSIS   影响因子和分区
语种英语
原始文献类型Article
关键词antibody immune response nucleocapsid protein SARS-CoV-2 vaccine
其他关键词SPIKE-PROTEIN ; IMMUNE-RESPONSES ; CORONAVIRUS ; VIRUS ; ANTIBODIES ; CHALLENGE ; INDUCTION ; INFECTION ; SEQUENCE ; DISEASE
摘要Background SARS-CoV-2 has spread worldwide causing more than 400 million people with virus infections since early 2020. Currently, the existing vaccines targeting the spike glycoprotein (S protein) of SARS-CoV-2 are facing great challenge from the infection of SARS-CoV-2 virus and its multiple S protein variants. Thus, we need to develop a new generation of vaccines to prevent infection of the SARS-CoV-2 variants. Compared with the S protein, the nucleocapsid protein (N protein) of SARS-CoV-2 is more conservative and less mutations, which also plays a vital role in viral infection. Therefore, the N protein may have the great potential for developing new vaccines. Methods The N protein of SARS-CoV-2 was recombinantly expressed and purified in Escherichia coli. Western Blot and ELISA assays were used to demonstrate the immunoreactivity of the recombinant N protein with the serum of 22 COVID-19 patients. We investigated further the response of the specific serum antibodies and cytokine production in BALB/c mice immunized with recombinant N protein by Western Blot and ELISA. Results The N protein had good immunoreactivity and the production of IgG antibody against N protein in COVID-19 patients was tightly correlated with disease severity. Furthermore, the N protein was used to immunize BALB/c mice to have elicited strong immune responses. Not only high levels of IgG antibody, but also cytokine-IFN-gamma were produced in the N protein-immunized mice. Importantly, the N protein immunization induced a high level of IgM antibody produced in the mice. Conclusion SARS-CoV-2 N protein shows a great big bundle of potentiality for developing a new generation of vaccines in fighting infection of SARS-CoV-2 and its variants.
资助项目Key Projects of Health and Hygiene [WKJ--ZJ--2138]
出版者WILEY
出版地HOBOKEN
ISSN0887-8013
EISSN1098-2825
卷号36期号:6页码:e24479
DOI10.1002/jcla.24479
页数10
WOS类目Medical Laboratory Technology
WOS研究方向Medical Laboratory Technology
WOS记录号WOS:000792094100001
收录类别SCIE ; SCOPUS ; PUBMED
URL查看原文
PubMed ID35527696
SCOPUSEID2-s2.0-85129514084
通讯作者地址[Zhu, Shanli]School of Basic Medical Science,Wenzhou Medical University,Wenzhou,China ; [Zhao, Kong-Nan]School of Basic Medical Science,Wenzhou Medical University,Wenzhou,China
Scopus学科分类Immunology and Allergy;Hematology;Public Health, Environmental and Occupational Health;Clinical Biochemistry;Medical Laboratory Technology;Biochemistry (medical);Microbiology (medical)
引用统计
被引频次:1[WOS]   [WOS记录]     [WOS相关记录]
文献类型期刊论文
条目标识符https://kms.wmu.edu.cn/handle/3ETUA0LF/148689
专题基础医学院(机能实验教学中心)
附属第二医院
通讯作者Zhu, Shanli; Zhao, Kong-Nan
作者单位
1.School of Basic Medical Science,Wenzhou Medical University,Wenzhou,China;
2.Department of Laboratory Medicine,The Sixth People Hospital of Wenzhou,Wenzhou,China;
3.Department of Obstetrics and Gynaecology,The Second Affiliated Hospital and Yuyin Children Hospital of Wenzhou Medical University,Wenzhou,China;
4.Australian Institute for Bioengineering and Nanotechnology,The University of Queensland,St Lucia,Australia
第一作者单位基础医学院(机能实验教学中心)
通讯作者单位基础医学院(机能实验教学中心)
第一作者的第一单位基础医学院(机能实验教学中心)
推荐引用方式
GB/T 7714
Feng, Weixu,Xiang, Yunru,Wu, Lianpeng,et al. Nucleocapsid protein of SARS-CoV-2 is a potential target for developing new generation of vaccine[J]. JOURNAL OF CLINICAL LABORATORY ANALYSIS,2022,36(6):e24479.
APA Feng, Weixu., Xiang, Yunru., Wu, Lianpeng., Chen, Zhuo., Li, Qingfeng., ... & Zhao, Kong-Nan. (2022). Nucleocapsid protein of SARS-CoV-2 is a potential target for developing new generation of vaccine. JOURNAL OF CLINICAL LABORATORY ANALYSIS, 36(6), e24479.
MLA Feng, Weixu,et al."Nucleocapsid protein of SARS-CoV-2 is a potential target for developing new generation of vaccine".JOURNAL OF CLINICAL LABORATORY ANALYSIS 36.6(2022):e24479.

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