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J Virol, April 1998, p. 3390-3393, Vol. 72, No. 4
Division of Molecular Virology, Baylor
College of Medicine, Houston, Texas 77030,1 and
Department of Microbiology and Immunology, Tulane University
Medical Center, New Orleans, Louisiana 701122
Received 1 October 1997/Accepted 16 December 1997
We have shown that rotavirus 2/6 viruslike particles composed of
proteins VP2 and VP6 (2/6-VLPs) administered to mice intranasally with
cholera toxin (CT) induced protection from rotavirus challenge, as
measured by virus shedding. Since it is unclear if CT will be approved
for human use, we evaluated the adjuvanticity of Escherichia coli heat-labile toxin (LT) and LT-R192G. Mice were inoculated intranasally with 10 µg of 2/6-VLPs combined with CT, LT, or
LT-R192G. All three adjuvants induced equivalent geometric mean titers
of rotavirus-specific serum antibody and intestinal immunoglobulin G
(IgG). Mice inoculated with 2/6-VLPs with LT produced significantly higher titers of intestinal IgA than mice given CT as the
adjuvant. All mice inoculated with 2/6-VLPs mixed with LT and
LT-R192G were totally protected (100%) from rotavirus challenge,
while mice inoculated with 2/6-VLPs mixed with CT showed a mean 91%
protection from challenge. The availability of a safe, effective
mucosal adjuvant such as LT-R192G will increase the practicality of
administering recombinant vaccines mucosally.
0022-538X/98/$04.00+0
Copyright © 1998, American Society for Microbiology. All rights reserved.
Rotavirus 2/6 Viruslike Particles Administered Intranasally with
Cholera Toxin, Escherichia coli Heat-Labile Toxin (LT),
and LT-R192G Induce Protection from Rotavirus Challenge
*
Corresponding author. Mailing address: Rm. 936E,
Division of Molecular Virology, Baylor College of Medicine, One Baylor
Plaza, Houston, TX 77030. Phone: (713) 798-3590. Fax: (713) 798-3586. E-mail: mconner{at}bcm.tmc.edu.
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