Construction of fusion gene vaccine of WT1 multi-epitope fused with stimulating epitope of mycobacterium tuberculosis heat shock protein 70 and its expression and immunogenicity.
- Author:
Wei-Wei TIAN
1
;
Zhen-Hua QIAO
;
Lin-Hua YANG
;
Hong-Wei WANG
;
Yan-Hong TANG
;
Si-Cheng BIAN
Author Information
1. Department of Hematology, The Second Hospital, Shanxi Medical University, Taiyuan, Shanxi Province, China.
- Publication Type:Journal Article
- MeSH:
Bacterial Proteins;
genetics;
immunology;
Epitopes;
genetics;
immunology;
Genetic Vectors;
HSP70 Heat-Shock Proteins;
genetics;
immunology;
Humans;
Immunodominant Epitopes;
Vaccines, DNA;
genetics;
immunology;
WT1 Proteins;
genetics;
immunology
- From:
Journal of Experimental Hematology
2011;19(2):485-490
- CountryChina
- Language:Chinese
-
Abstract:
This study was purposed to construct a fusion DNA vaccine containing WT1 multi-epitope and stimulating epitope of mycobacterium tuberculosis heat shock protein 70 and to detect its expression and immunogenicity. On the basis of published data, a multi-epitope gene (Multi-WT1) containing three HLA *0201-restricted CTL epitopes: one HLA*2402-restricted CTL epitope, two Th epitopes and one universal Th Pan-DR epitope (PADRE) was constructed. DNA-coding sequence was modified by Computer-Aided Design (CAD) to optimize proteasome-mediated epitope processing through the introduction of different amino acid spacer sequences. The synthetic nucleotide sequence was then inserted into an eukaryotic vector to construct the plasmid pcDNA3.1-WT1.For enhancing CTL activity, HSP70 fragment including stimulatory domain P407-426 was amplified by PCR from mycobacterial HSP70 gene and cloned into pcDNA3.1(+). Then Multi-WT1 was fused to the N-terminal of pcDNA3.1-mHSP70(407-426) to make the multi-epitope fusion gene vaccine pcDNA3.1-WT1-mHSP70(407-426). HEK-293T cells were transfected with this vaccine and the expressed product was identified by RT-PCR. Enzyme-linked immunospot assay (ELISPOT) was used to evaluate the immunological responses elicited by vaccine. The results showed that the most of WT1 epitopes could be correctly cleaved which was confirmed by software Net Chop 3.1 and PAPROCIanalysis. RT-PCR showed correct expression of target gene in HEK293T cells and ELISPOT showed specific T-cell responses. It is concluded that the eukaryotic expression vector PcDNA3.1-WT1-mHSP70(407-426) fusion gene has been successfully constructed and the immunity response is also elicited, which is a good candidate for further research of DNA vaccine.
