Induction of protective immunity by synthetic Vibrio cholerae hexasaccharide derived from V-cholerae O1 ogawa lipopolysaccharide bound to a protein carrier

被引:64
作者
Chernyak, A
Kondo, S
Wade, TK
Meeks, MD
Alzari, PM
Fournier, JM
Taylor, RK
Kovác, P
Wade, WF
机构
[1] NIDDKD, Med Chem Lab, NIH, Bethesda, MD 20892 USA
[2] Dartmouth Coll Sch Med, Dept Microbiol & Immunol, Lebanon, NH 03755 USA
[3] Josai Univ, Sch Pharmaceut Sci, Dept Microbiol, Sakado, Saitama 35002, Japan
[4] Inst Pasteur, Unite Biochim Struct, CNRS, Unite Rech Associe 2185, Paris, France
[5] Inst Pasteur, Unite Cholera & Vibr, Ctr Natl Reference Vibr & Cholera, Paris, France
关键词
D O I
10.1086/339583
中图分类号
R392 [医学免疫学]; Q939.91 [免疫学];
学科分类号
100102 ;
摘要
Synthetic antigens that mimic the terminal hexasaccharide epitope of the O-specific polysaccharide of Vibrio cholerae O1, serotype Ogawa, were conjugated to bovine serum albumin (BSA). Conjugates with carbohydrate-to-carrier molar ratios of 15.5:1, 9.2: 1, and 4.6: 1 were tested for immunogenicity and efficacy in mice. The role of preimmunity to BSA and the use of adjuvant in the generation of the serologic response to the O-specific polysaccharide and protection against virulent V. cholerae was examined. Preimmunity to BSA did not affect the anti-Ogawa titers but seemed to enhance the protective capacity of antiserum. All 3 conjugates were immunogenic, but adjuvant was effective at inducing higher and earlier antibody responses. In tertiary serum samples, a correlation was found between vibriocidal activity and protection. The protective capacity of antiserum was evident in serum from mice immunized with all conjugates, but it was highest in the groups that received the conjugate with the lowest level of substitution. Further studies are required to increase understanding of the reason for differential protection.
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页码:950 / 962
页数:13
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