HPV16 mutant E6/E7 construct is protective in mouse model

被引:1
作者
Goodarzi, Maryam Moazami [1 ]
Mosayebi, Ghasem [2 ]
Ganji, Ali [2 ]
Raoufi, Ehsan [3 ]
Sadelaji, Samira [4 ]
Babaei, Saeid [5 ]
Abtahi, Hamid [6 ]
机构
[1] Arak Univ Med Sci, Fac Med, Dept Med Biotechnol, Arak, Iran
[2] Arak Univ Med Sci, Sch Med, Dept Microbiol & Immunol, Arak, Iran
[3] Iran Univ Med Sci, Vaccine Res Ctr, Tehran, Iran
[4] Arak Univ Med Sci, Fac Med, Dept Microbiol & Immunol, Arak, Iran
[5] Arak Univ Med Sci, Sch Med, Dept Anat, Arak, Iran
[6] Arak Univ Med Sci, Mol & Med Res Ctr, Arak, Iran
关键词
Recombinant protein; DNA vaccine; HPV-16; Therapeutic vaccine; Tumor-specific antigens (TSAs); Fusion gene; Prime-boost strategy; CD4+T-CELL IMMUNITY; CERVICAL-CANCER; E7; PROTEIN; E6; VACCINATION; EXPRESSION; RESPONSES; TYPE-16;
D O I
10.1186/s12896-024-00893-y
中图分类号
Q81 [生物工程学(生物技术)]; Q93 [微生物学];
学科分类号
071005 ; 0836 ; 090102 ; 100705 ;
摘要
Background Human papillomavirus type 16 (HPV-16) infection is strongly associated with considerable parts of cervical, neck, and head cancers. Performed investigations have had moderate clinical success, so research to reach an efficient vaccine has been of great interest. In the present study, the immunization potential of a newly designed HPV-16 construct was evaluated in a mouse model. Results Initially, a construct containing HPV-16 mutant (m) E6/E7 fusion gene was designed and antigen produced in two platforms (i.e., DNA vaccine and recombinant protein). Subsequently, the immunogenicity of these platforms was investigated in five mice) C57BL/6 (groups based on several administration strategies. Three mice groups were immunized recombinant protein, DNA vaccine, and a combination of them, and two other groups were negative controls. The peripheral blood mononuclear cells (PBMCs) proliferation, Interleukin-5 (IL-5) and interferon-gamma (IFN-gamma) cytokines, IgG1 and IgG2a antibody levels were measured. After two weeks, TC-1 tumor cells were injected into all mice groups, and subsequently further analysis of tumor growth and metastasis and mice survival were performed according to the schedule. Overall, the results obtained from in vitro immunology and tumor cells challenging assays indicated the potential of the mE6/E7 construct as an HPV16 therapeutic vaccine candidate. The results demonstrated a significant increase in IFN-gamma cytokine (P value < 0.05) in the Protein/Protein (D) and DNA/Protein (E) groups. This finding was in agreement with in vivo assays. Control groups show a 10.5-fold increase (P value < 0.001) and (C) DNA/DNA group shows a 2.5-fold increase (P value < 0.01) in tumor growth compared to D and E groups. Also, a significant increase in survival of D and E (P value < 0.001) and C (P value < 0.01) groups were observed. Conclusions So, according to the findings, the recombinant protein could induce stronger protection compared to the DNA vaccine form. Protein/Protein and DNA/Protein are promising administration strategies for presenting this construct to develop an HPV-16 therapeutic vaccine candidate.
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页数:11
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