Polyclonal BALB/C mouse and New Zealand White rabbit anti-idiotypic an
tibodies were raised by immunization with a protein G-purified burro a
nti-saxitoxin IgG antibody preparation. Following absorption of non-an
ti-idiotype reactivity, murine and rabbit IgG were purified by protein
A chromatography and used to immunize BALB/C mice for the induction o
f anti-saxitoxin antibody responses. Unconjugated BALB/C anti-idiotype
s did not induce significant anti-saxitoxin reactivity in BALB/C mice,
even after repeated immunizations. However, BALB/C mice immunized wit
h purified BALB/C anti-idiotypes conjugated to keyhole limpet hemocyan
in, or with purified, unconjugated rabbit anti-idiotypes, as aluminum
hydroxide precipitates, induced significant and specific anti-saxitoxi
n immune responses. Saxitoxin, a sodium channel blocker, can protect c
ells treated with veratridine and ouabain, whose respective actions ar
e to open sodium channels and to block the activity of Na/K-ATPase. Th
e anti-idiotype-induced anti-saxitoxin antibodies inhibited saxitoxin
from protecting against cell death induced by veratridine and ouabain
treatment. These and other published experimental results strengthen t
he concept of anti-idiotype-based vaccines in eliciting protective imm
unity against a variety of low molecular weight, nonproteinaceous biol
ogical and chemical toxins, whose extreme toxicity does not allow thei
r use as safe immunogens.