It was determined whether microencapsulation of rotavirus enhanced vir
us-specific immunity in mice. Combinations of several water-soluble an
ionic polymers and amines were tested for their capacity to form micro
capsules which were stable in the presence of simulated gastric acid.
Using the combinations of sodium alginate and spermine hydrochloride o
r sodium chondroitin sulfate and spermine hydrochloride we found that
microcapsules (1) captured infectious rotavirus, (2) penetrated into t
he persisted in gut-associated lymphoid tissue (GALT) after oral inocu
lation, (3) delivered rotavirus antigen to GALT at levels greater than
those detected after oral inoculation with free virus, and (4) enhanc
ed the virus-specific humoral immune response after oral or parenteral
immunization. (C) 1994 Academic Press, Inc.