ORAL INOCULATION OF MICE WITH LOW-DOSES OF MICROENCAPSULATED, NONINFECTIOUS ROTAVIRUS INDUCES VIRUS-SPECIFIC ANTIBODIES IN GUT-ASSOCIATED LYMPHOID-TISSUE
Ca. Khoury et al., ORAL INOCULATION OF MICE WITH LOW-DOSES OF MICROENCAPSULATED, NONINFECTIOUS ROTAVIRUS INDUCES VIRUS-SPECIFIC ANTIBODIES IN GUT-ASSOCIATED LYMPHOID-TISSUE, The Journal of infectious diseases, 172(3), 1995, pp. 870-874
The capacity of an aqueous-based system of microencapsulation to enhan
ce virus-specific humoral immune responses was evaluated in mice orall
y inoculated with noninfectious rotavirus (simian rotavirus strain RRV
). Mice were orally inoculated with 1.75 or 0.35 mu g of inactivated R
RV (iRRV) or microencapsulated iRRV. Sera, intestinal contents, and or
gan cultures of gut-associated lymphoid tissues (GALT) were tested for
the presence of rotavirus-specific antibodies. Virus-specific IgA was
produced by small intestine lamina propria lymphocytes in animals ino
culated with 1.75 or 0.35 mu g of microencapsulated virus, but not in
mice inoculated with unencapsulated virus. Virus-specific IgA in sera
and intestinal contents were not predictive of intestinal organ cultur
e responses. Microencapsulation may be an efficient way of inducing vi
rus-specific immune responses in GALT after oral inoculation with smal
l quantities of viral antigen. In addition, delayed release of virus f
rom microcapsules may obviate the need for booster immunizations.