Effect of Water-Based Microencapsulation on Protection against EDIM Rotavirus Challenge in Mice

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Published inJournal of Virology Vol. 72; no. 5; pp. 3859 - 3862
Main Authors Moser, C A, Speaker, T J, Offit, P A
Format Journal Article
LanguageEnglish
Published United States American Society for Microbiology 01.05.1998
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We determined the capacity of microcapsules formed by the combination of sodium alginate, an aqueous anionic polymer, and spermine hydrochloride, an aqueous cationic amine, to enhance protection against rotavirus challenge in mice. Adult BALB/c mice were orally inoculated with either free or microencapsulated rotavirus (simian rotavirus strain RRV) and challenged 6 or 16 weeks later with murine rotavirus strain EDIM. Virus-specific humoral immune responses were determined at the time of challenge and 4 days after challenge by intestinal fragment culture. We found that spermine-alginate microcapsules enhanced protection against challenge 16 weeks after immunization but not 6 weeks after immunization. Quantities of virus-specific immunoglobulin A produced by small intestinal lamina propria lymphocytes were correlated with the degree of protection against challenge afforded by spermine-alginate microcapsules. Possible mechanisms by which microcapsules enhance protection against rotavirus challenge are discussed.
ABSTRACT We determined the capacity of microcapsules formed by the combination of sodium alginate, an aqueous anionic polymer, and spermine hydrochloride, an aqueous cationic amine, to enhance protection against rotavirus challenge in mice. Adult BALB/c mice were orally inoculated with either free or microencapsulated rotavirus (simian rotavirus strain RRV) and challenged 6 or 16 weeks later with murine rotavirus strain EDIM. Virus-specific humoral immune responses were determined at the time of challenge and 4 days after challenge by intestinal fragment culture. We found that spermine-alginate microcapsules enhanced protection against challenge 16 weeks after immunization but not 6 weeks after immunization. Quantities of virus-specific immunoglobulin A produced by small intestinal lamina propria lymphocytes were correlated with the degree of protection against challenge afforded by spermine-alginate microcapsules. Possible mechanisms by which microcapsules enhance protection against rotavirus challenge are discussed.
Author Charlotte A. Moser
Tully J. Speaker
Paul A. Offit
AuthorAffiliation Section of Infectious Diseases, The Children’s Hospital of Philadelphia, 1 University of Pennsylvania School of Medicine, 3 and Wistar Institute of Anatomy and Biology, 4 Philadelphia, Pennsylvania 19104, and Temple University School of Pharmacy, Philadelphia, Pennsylvania 19140 2
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Corresponding author. Mailing address: Section of Infectious Diseases, The Children’s Hospital of Philadelphia, Abramson Research Center, Rm. 1205A, 34th St. and Civic Center Blvd., Philadelphia, PA 19104. Phone: (215) 590-5152 or (215) 590-2186. Fax: (215) 590-2025. E-mail: Moser@email.chop.edu.
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We determined the capacity of microcapsules formed by the combination of sodium alginate, an aqueous anionic polymer, and spermine hydrochloride, an aqueous...
ABSTRACT We determined the capacity of microcapsules formed by the combination of sodium alginate, an aqueous anionic polymer, and spermine hydrochloride, an...
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SubjectTerms Alginates
Animal Viruses
Animals
Antibodies, Viral - biosynthesis
Biocompatible Materials
Cell Line
Cercopithecus aethiops
Disease Models, Animal
Drug Compounding
Female
Glucuronic Acid
Hexuronic Acids
Immunoglobulin A - biosynthesis
Intestine, Small - cytology
Intestine, Small - immunology
Lymphocytes - immunology
Mice
Mice, Inbred BALB C
Rotavirus - immunology
Rotavirus Infections - immunology
Rotavirus Infections - prevention & control
Time Factors
Vaccination - methods
Water
Title Effect of Water-Based Microencapsulation on Protection against EDIM Rotavirus Challenge in Mice
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