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Journal of Virology, November 1998, p. 9233-9246, Vol. 72, No. 11
0022-538X/98/$04.00+0
Copyright © 1998, American Society for Microbiology. All rights reserved.
Subunit Rotavirus Vaccine Administered Parenterally
to Rabbits Induces Active Protective Immunity
Max
Ciarlet,1
Sue
E.
Crawford,1
Christopher
Barone,1
Andrea
Bertolotti-Ciarlet,1
Robert F.
Ramig,1
Mary K.
Estes,1 and
Margaret
E.
Conner1,2,*
Division of Molecular Virology, Baylor
College of Medicine,1 and
Veterans
Affairs Medical Center,2 Houston, Texas 77030
Received 23 February 1998/Accepted 24 July 1998
Virus-like particles (VLPs) are being evaluated as a candidate
rotavirus vaccine. The immunogenicity and protective efficacy of
different formulations of VLPs administered parenterally to rabbits
were tested. Two doses of VLPs (2/6-, G3 2/6/7-, or P[2], G3
2/4/6/7-VLPs) or SA11 simian rotavirus in Freund's adjuvants, QS-21
(saponin adjuvant), or aluminum phosphate (AlP) were administered. Serological and mucosal immune responses were evaluated in all vaccinated and control rabbits before and after oral challenge with
103 50% infective doses of live P[14], G3 ALA lapine
rotavirus. All VLP- and SA11-vaccinated rabbits developed high levels
of rotavirus-specific serum and intestinal immunoglobulin G (IgG)
antibodies but not intestinal IgA antibodies. SA11 and 2/4/6/7-VLPs
afforded similar but much higher mean levels of protection than 2/6/7-
or 2/6-VLPs in QS-21. The presence of neutralizing antibodies to VP4
correlated (P < 0.001, r = 0.55;
Pearson's correlation coefficient) with enhanced protection rates,
suggesting that these antibodies are important for protection. Although
the inclusion of VP4 resulted in higher mean protection levels, high
levels of protection (87 to 100%) from infection were observed in
individual rabbits immunized with 2/6/7- or 2/6-VLPs in Freund's
adjuvants. Therefore, neither VP7 nor VP4 was absolutely required to
achieve protection from infection in the rabbit model when Freund's
adjuvant was used. Our results show that VLPs are immunogenic when
administered parenterally to rabbits and that Freund's adjuvant is a
better adjuvant than QS-21. The use of the rabbit model may help
further our understanding of the critical rotavirus proteins needed to
induce active protection. VLPs are a promising candidate for a
parenterally administered subunit rotavirus vaccine.
*
Corresponding author. Mailing address: 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.
Journal of Virology, November 1998, p. 9233-9246, Vol. 72, No. 11
0022-538X/98/$04.00+0
Copyright © 1998, American Society for Microbiology. All rights reserved.
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