Objective: To construct recombinant MVA carrying Plasmodium falciparum (Pf) arm1 gene and evaluate its immune characteristic in mice. Methods: MVA recombination vector p III dHR. ssp/E which contains Pf ama1 gene segment was built and used to transfect MVA infected BHK21 cells, recombinant viruses carrying host range gene k1l were selected by serially infecting RK13 cells. rMVA/E(K1L) was used to reinfect BHK21 under nonselective growth conditions, k1l was removed by intra-genomic homologous recombination and the final rMVA/E was harvested. rMVA/E genome sequence and AMA1 expression were identified by PCR, IFA and Western blot. Groups of BALB/c mice were immunized with different dosages of purified rMVA/E, level of anti-AMA1 IgG antibodies and their sub-isotypes were then determined by ELISA, and in vitro proliferation of splenocytes was examined. Results: Stable recombinant MVA carrying Pf ama1 gene segment had been selected. After three intraperitoneal administration of different doses (107-108 TCID50) rMVA/E, similar levels of IgG were induced in BALB/c mice of which IgG2a was dominant. After re-stimulating with AMA1 antigen all the immune splenocytes produced significant reminiscent reaction. Conclusion: Recombinant MVA stably carrying Pf ama1 gene had been successfully constructed and rMVA/E could elicit AMA1 specific immune response in mice.
|Original language||English (US)|
|Number of pages||4|
|Journal||Chinese Journal of Microbiology and Immunology|
|State||Published - Oct 2003|
All Science Journal Classification (ASJC) codes
- Immunology and Microbiology(all)
- Microbiology (medical)