Effective mucosal immunization against respiratory syncytial virus using purified F protein and a genetically detoxified cholera holotoxin, CT-E29H

• Published in: Vaccine 2000-06, Vol.18 (24), p.2723-2734
• Main Authors: Tebbey, Paul W, Scheuer, Catherine A, Peek, Joel A, Zhu, Duzhang, LaPierre, Natisha A, Green, Bruce A, Phillips, Eric D, Ibraghimov, Alexander R, Eldridge, John H, Hancock, Gerald E
• Format: Article
• Language: English
• Subjects: AF protein; Animals; Antigens, Viral - immunology; Biological and medical sciences; Bronchoalveolar Lavage; Cholera toxin; Cholera Toxin - immunology; Electrophoresis, Polyacrylamide Gel; Enzyme-Linked Immunosorbent Assay; F protein; Female; Fundamental and applied biological sciences. Psychology; HN Protein; holotoxin CT-E29H; Immunity, Mucosal; Lung - virology; Mice; Mice, Inbred BALB C; Microbiology; Nasal Mucosa - virology; respiratory syncytial virus; Respiratory Syncytial Viruses - immunology; RSV; Vaccines; Vaccines, antisera, therapeutical immunoglobulins and monoclonal antibodies; Vibrio cholerae; Viral Envelope Proteins; Viral Proteins - immunology; Viral Vaccines - immunology; Virology
• ISSN: 0264-410X; 1873-2518
• DOI: 10.1016/S0264-410X(00)00058-X

We exploited the powerful adjuvant properties of cholera holotoxin (CT) to create a mucosally administered subunit vaccine against respiratory syncytial virus (RSV). A genetically detoxified mutant CT with an E to H substitution at amino acid 29 of the CT-A1 subunit (CT-E29H) was compared to wild type CT for toxicity and potential use as an intranasal (IN) adjuvant for the natural fusion (F) protein of RSV. When compared to CT the results demonstrated that: (1) CT-E29H binding to GM1 ganglioside was equivalent, (2) ADP-ribosylation of agmatine was 11.7%, and (3) toxicity was attenuated in both Y-1 adrenal (1.2%) and patent mouse gut weight assays. IN vaccination with F protein formulated with CT-E29H induced serum anti-CT and anti-F protein antibodies that were comparable to those obtained after vaccination with equivalent doses of CT. Vaccinations containing CT-E29H at doses of 0.1 μg were statistically equivalent to 1.0 μg in enhancing responses to F protein. Antigen-specific mucosal IgA and anti-RSV neutralizing antibodies were detected in nasal washes and sera, respectively, of mice that had received F protein and 0.1 or 1.0 μg of CT-E29H. Anti-F protein IgA was not detected in the nasal washes from mice IN vaccinated with 0.01 μg CT-E29H or IM with F protein adsorbed to AlOH adjuvant. In addition, the formulation of purified F protein and CT-E29H (0.1 and 1.0 μg) facilitated protection of both mouse lung and nose from live RSV challenge. Collectively, the data have important implications for vaccine strategies that use genetically detoxified mutant cholera holotoxins for the mucosal delivery of highly purified RSV antigens.