Cryz S J, Que J U, Levine M M, Wiedermann G, Kollaritsch H
Swiss Serum and Vaccine Institute, Berne.
Infect Immun. 1995 Apr;63(4):1336-9. doi: 10.1128/iai.63.4.1336-1339.1995.
The safety and immunogenicity of the live oral attenuated vaccine strains vibrio cholerae CVD 103-HgR and Salmonella typhi Ty21a were evaluated alone or in a combined bivalent formulation in four groups composed of 185 healthy European adults. All presentations were well tolerated. The serum anti-S. typhi lipopolysaccharide immunoglobulin G and immunoglobulin A antibody responses were comparable for all groups (66 to 72% seroconversion). The serum vibriocidal antibody seroconversion rate ranged from 78 to 92.5% (P > 0.05) among the groups. However, the peak and geometric mean vibriocidal antibody titers were significantly higher (P < 0.005) in the groups which received the bivalent formulation along with two doses of Ty21a than in the group which received CVD 103-HgR followed by two doses of killed Escherichia coli K-12 placebo. The ingestion of a placebo shortly after CVD 103-HgR may have suppressed the magnitude of the immune response. These findings demonstrate the feasibility of producing multivalent live oral attenuated vaccines.
在由185名健康欧洲成年人组成的四组中,对霍乱弧菌CVD 103-HgR和伤寒沙门氏菌Ty21a减毒活口服疫苗株单独或联合二价制剂的安全性和免疫原性进行了评估。所有受试制剂耐受性良好。所有组的血清抗伤寒沙门氏菌脂多糖免疫球蛋白G和免疫球蛋白A抗体反应相当(血清转化率为66%至72%)。各实验组的血清杀弧菌抗体血清转化率在78%至92.5%之间(P>0.05)。然而,与接受CVD 103-HgR后再接种两剂灭活大肠杆菌K-12安慰剂的组相比,接受二价制剂及两剂Ty21a的组中,杀弧菌抗体的峰值和几何平均滴度显著更高(P<0.005)。在CVD 103-HgR后不久摄入安慰剂可能抑制了免疫反应的强度。这些发现证明了生产多价减毒活口服疫苗的可行性。