Improving potency of Chlamydia trachomatis major outer membrane protein muli-epitope DNA vaccine by fusion with human papillomavirues 6b L1
Autor: | Lifang Zhang, Jun Chen, Zhao-hui Shi, Wen Xu, Ruifeng Meng, Wenci Gong, Shanli Zhu |
---|---|
Rok vydání: | 2011 |
Předmět: |
Chlamydia
business.industry medicine.medical_treatment General Medicine bacterial infections and mycoses urologic and male genital diseases medicine.disease_cause medicine.disease Virology Fusion protein female genital diseases and pregnancy complications General Biochemistry Genetics and Molecular Biology Epitope DNA vaccination law.invention Plasmid law Poster Presentation medicine Recombinant DNA bacteria business Chlamydia trachomatis Adjuvant |
Zdroj: | BMC Proceedings |
ISSN: | 1753-6561 |
Popis: | Effective adjuvants are needed to design effective vaccines against Chlamydia trachomatis (Ct). The aim of this study was to observe the immune response stimulated by inoculation of a DNA vaccine encoding a fusion protein comprising multiple Ct major outer membrane protein (MOMP) epitopes and human papillomavirus 6b L1 (HPV 6b L1) as the basis for designing a novel DNA vaccine against genital Chlamydia infections. The recombinant sequence encoding MOMP multi-epitopes was tandemly inserted and engaged downstream of HPV 6b L1 to construct a plasmid vaccine. COS-7 cells were transfected with pcDNA3.1(+)/Ct MOMP 168 encoding the Ct MOMP multi-epitope gene and co-expressed with the nucleic vaccine plasmid pcDNA3.1(+)/HPV 6b L1/Ct MOMP 168, which contains both the HPV 6b L1 and Ct MOMP multi-epitope genes. In addition, BALB/ c mice were inoculated intramuscularly (i.m.) with pcDNA3.1(+)/HPV 6b L1/Ct MOMP 168 or pcDNA3.1(+)/Ct MOMP 168. Serum IgG and secretory IgA (sIgA) in vaginal washes were then measured. The expression of HPV 6b L1/Ct MOMP multi-epitope was confirmed by western blotting, confocal microscopy and RT-PCR. Mice vaccinated with pcDNA3.1(+)/HPV 6b L1/Ct MOMP 168 had significantly higher IgG and sIgA antibody titers than pcDNA3.1(+)/Ct MOMP 16 controls. The results show that genetic fusion of the molecular adjuvant HPV 6b L1 to Ct MOMP 168 significantly increases the antigen-specific antibody response induced by the Ct MOMP 168 DNA vaccine. |
Databáze: | OpenAIRE |
Externí odkaz: |