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Phase 1 and Phase 2 Studies of Salmonella Enterica Serovar Paratyphi A O-specific Polysaccharide-tetanus Toxoid Conjugates in Adults, Teenagers, and 2- to 4-year-old Children in Vietnam

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Journal Infect Immun
Date 2000 Feb 26
PMID 10678970
Citations 29
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Abstract

Salmonella enterica serovar Paratyphi A O-specific polysaccharide (O-SP) was activated with 1-cyano-4-dimethylaminopyridinium tetrafluoroborate (CDAP) and bound to tetanus toxoid (TT) with adipic acid dihydrazide as a linker (SPA-TT(1)) or directly (SPA-TT(2)). In mice, these two conjugates elicited high levels of immunoglobulin G (IgG) anti-lipopolysaccharide (LPS) in serum with bactericidal activity (E. Konadu, J. Shiloach, D. A. Bryla, J. B. Robbins, and S. C. Szu, Infect. Immun. 64:2709-2715, 1996). The safety and immunogenicity of the two conjugates were then evaluated sequentially in Vietnamese adults, teenagers, and 2- to 4-year-old children. None of the vaccinees experienced significant side effects, and all had preexisting LPS antibodies. At 4 weeks after injection, there were significant increases of the geometric mean IgG and IgM anti-LPS levels in the adults and teenagers: both conjugates elicited a greater than fourfold rise in the IgG anti-LPS level in serum in >/=80% of the volunteers. SPA-TT(2) elicited slightly higher, though not statistically significantly, levels of IgG anti-LPS than did SPA-TT(1) in these age groups. Accordingly, only SPA-TT(2) was evaluated in the 2- to 4-year-old children. On a random basis, one or two injections were administered 6 weeks apart to the children. No significant side effects were observed, and the levels of preexisting anti-LPS in serum were similar in children of all ages. A significant rise in the IgG anti-LPS titer was elicited by the first injection (P = 0.0001); a second injection did not elicit a booster response. Representative sera from all groups had bactericidal activity that could be adsorbed by S. enterica serovar Paratyphi A LPS.

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References
1.
Tran T, Bethell D, Nguyen T, Wain J, To S, Le T . Short course of ofloxacin for treatment of multidrug-resistant typhoid. Clin Infect Dis. 1995; 20(4):917-23. View

2.
Lepage P, Bogaerts J, Van Goethem C, Ntahorutaba M, Nsengumuremyi F, Hitimana D . Community-acquired bacteraemia in African children. Lancet. 1987; 1(8548):1458-61. DOI: 10.1016/s0140-6736(87)92207-0. View

3.
FOUQUEY C, Polonsky J, Lederer E, Westphal O, LUDERITZ O . Synthesis of 3,6-dideoxy-D-ribo-hexose (3, 6-dideoxy-D-glucose) and its identification with paratose. Nature. 1958; 182(4640):944. DOI: 10.1038/182944a0. View

4.
Nesbitt A, Mirza N . Salmonella septicaemias in Kenyan children. J Trop Pediatr. 1989; 35(1):35-9. DOI: 10.1093/tropej/35.1.35. View

5.
Bock K, Meldal M, Bundle D, Iversen T, Garegg P, Norberg T . The conformation of Salmonella O-antigenic polysaccharide chains of serogroups A, B, and D1 predicted by semi-empirical, Hard-Sphere (HSEA) calculations. Carbohydr Res. 1984; 130:23-34. DOI: 10.1016/0008-6215(84)85267-2. View