An adjuvanted inactivated murine cytomegalovirus (MCMV) vaccine induces potent and long-term protective immunity against a lethal challenge with virulent MCMV

• Published in: BMC infectious diseases 2014-04, Vol.14 (1), p.195-195, Article 195
• Main Authors: Wang, Huadong, Yao, Yanfeng, Huang, Chaoyang, Fu, Xingxing, Chen, Quanjiao, Zhang, Hongbo, Chen, Jianjun, Fang, Fang, Xie, Zhenyuan, Chen, Ze
• Format: Article
• Language: English
• Subjects: Adjuvants, Immunologic; Analysis; Animals; Antigens; Cell culture; Clinical trials; Cytomegalovirus; Cytomegalovirus Vaccines - immunology; Female; Formaldehyde; Health aspects; Herpesviridae Infections - immunology; Herpesviridae Infections - prevention & control; Human cytomegalovirus; Immune response; Infections; Medical research; Medicine, Experimental; Mice; Mice, Inbred BALB C; Mortality; Murine cytomegalovirus; Muromegalovirus - immunology; Proteins; Rodents; Specific Pathogen-Free Organisms; Vaccines; Vaccines, Inactivated - immunology; Viral infections; Viral Load
• ISSN: 1471-2334; 1471-2334
• DOI: 10.1186/1471-2334-14-195

Human cytomegalovirus (HCMV) is a ubiquitous pathogen that causes serious problems in immunocompromised or immunologically immature hosts. Vaccination is the preferred approach for prevention of HCMV infection, but so far no approved HCMV vaccine is available. In this study, we assessed the immunogenicity and protective immunity of a formalin-inactivated murine cytomegalovirus vaccine (FI-MCMV) in a mouse model in combination with adjuvants MF59, alum, or chitosan. Specific-pathogen-free BALB/c mice aged 6-8 weeks were immunized twice, 3 weeks apart, with various doses of FI-MCMV (0.25 μg, 1 μg, 4 μg) with or without adjuvant. Mice were challenged with a lethal dose (5 × LD50) of a more virulent mouse salivary gland-passaged MCMV 3 weeks after the second immunization. The protective immunity of the vaccine was evaluated by determining the survival rates, residual spleen and salivary gland viral loads, body weight changes, and serum anti-MCMV IgG titers. Immunization with FI-MCMV vaccine induced a high level of specific antibody response. Antigen sparing was achieved by the addition of an adjuvant, which significantly enhanced the humoral response to vaccine antigens with a wide range of doses. The level of live virus detected in the spleen on day 5 and in the salivary glands on day 21 after the lethal challenge was significantly lower in adjuvant-treated groups than in controls. Survival rates in adjuvant-treated groups also increased significantly. Furthermore, these protective immune responses were sustained for at least 6 months following immunization. These results show that inactivated MCMV vaccine is effective, and that the adjuvanted FI-MCMV vaccine provides more effective and longer-term protection than the adjuvant-free vaccine.