Ma. Suckow et al., ORAL IMMUNIZATION OF RABBITS AGAINST PASTEURELLA-MULTOCIDA WITH AN ALGINATE MICROSPHERE DELIVERY SYSTEM, Journal of biomaterials science. Polymer ed., 8(2), 1996, pp. 131-139
Oral delivery of microencapsulated antigens is a potential means to va
ccinate rabbits against Pasteurella multocida, a common bacterial path
ogen. Groups of five rabbits were dosed orally on days 0, 7, and 14 wi
th alginate microspheres prepared to contain no added protein, 5 mg of
a potassium thiocyanate extract of P. multocida (PTE), or 5 mg of PTE
with 200 mu g of cholera toxin (CT). In addition, groups were dosed o
rally with 5 mg of soluble PTE with or without 200 mu g CT, intranasal
ly (IN) with 1 mg of soluble PTE, or with saline. Serum and nasal lava
ge samples collected prior to initial immunization and 10, 16, and 21
days later were assayed by ELISA for anti-PTE IgG and IgA. Strong nasa
l lavage IgA and serum IgG activities were found in samples From rabbi
ts immunized with PTE IN or orally when incorporated into microspheres
. Addition of CT did not significantly enhance either response. To exa
mine the development of protective immunity, groups were similarly imm
unized and challenge-exposed IN on day 16 with 10(6) CFU of P. multoci
da. One week later, rabbits were euthanized, and specimens from the lu
ngs, nasopharynx, liver, and inner ear were cultured for P multocida.
Less severe infections of the lung and nasopharynx developed in rabbit
s immunized with PTE IN or orally in microspheres, with or without add
ed CT. In addition, culture of liver and tympanic bullae samples from
these rabbits yielded growth of P. multocida less frequently compared
to other P multocida-challenged rabbits. Coadministration of CT and PT
E did not significantly improve protective immunity to challenge.