Drug-specific antibodies have been used clinically to treat digoxin or
colchicine overdose. The lethal dose of tricyclic antidepressants (TC
As) is 100 times higher, and will require higher doses of antibodies (
up to several g/kg) to reverse toxicity. Preliminary studies suggest t
hat this is feasible. High affinity TCA-specific monoclonal Fab' or po
lyclonal Fab fragments rapidly reverse the cardiovascular toxicity of
the TCA desipramine (DMI) in rats, and prolong survival. TCA-specific
Fab' or Fab is generally well tolerated in rats, but doses several tim
es higher than anticipated for human use may have adverse effects. Com
bining Fab with standard therapies for TCA overdose, such as NaHCO3, c
an reduce the required Fab dose. As an alternative, a recombinant sing
le chain Fv fragment (sFv), one half the size of Fab, has been cloned
which retains a high affinity for DMI and is able to alter DMI distrib
ution in vivo. Because sFv has a shorter elimination half-life and mor
e extensive renal excretion than Fab, it may have therapeutic advantag
es.