Gbl. Harrison et al., Duration of immunity, efficacy and safety in sheep of a recombinant Taeniaovis vaccine formulated with saponin or selected adjuvants, VET IMMUNOL, 70(3-4), 1999, pp. 161-172
The efficacy and safety of a recombinant Taenia ovis protein was tested in
sheep using 13 different adjuvant formulations, including oil adjuvants, al
uminium salts, saponin, Iscoms and DEAE-dextran. The oil adjuvants, saponin
and DEAE-dextran gave the highest antibody responses and greatest degree o
f protection against challenge infection with T. ovis eggs. Duration of imm
unity studies with a saponin based vaccine showed that highly significant p
rotection (>90% reduction of cyst numbers) was achieved when sheep were cha
llenge infected one month after immunisation. Significant protection (79%)
was still present when sheep were challenged 6 months after immunisation, T
he optimum dose for this batch of saponin was 10 mg, which stimulated a pea
k antibody titre of 38,400, 4 weeks after immunisation and did not cause in
jection site reactions. Dialysed saponin was shown to retain its adjuvant p
roperties and allowed an increase in dose to 30 mg without site reaction, r
esulting in a peak antibody titre of 51,200. (C) 1999 Elsevier Science B.V.
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