Following the identification of antibodies (Abs) as agents of immunity
, it was hypothesized that individuals could be both (1) protected aga
inst disease by the transfer of unmodified Ab (passive immunization),
and (2) cured of established disease by Ab armed with cytotoxic agents
(immunotherapy). The development of monoclonal antibody (mAb) technol
ogy in 1975 reinvigorated these ideas. Although passive immunization h
as been practiced with great success for many years, successful tissue
targeting by systemically delivered immunotoxins in humans has been d
ocumented in only a few cases. New modes of drug delivery, engineered
for mAb-based products, may enable new applications of passive immuniz
ation and may provide improved tissue targeting for immunotherapy. By
allowing sustained and tissue-localized delivery of mAb-conjugates, co
ntrolled-release polymers may play an important role in this effort. T
his article reviews the use of mAb in treating and preventing human di
sease, as well as the pharmacokinetics of Ab delivery. Two areas where
controlled Ab release may yield new therapies are highlighted: sustai
ned passive immunization of the mucus secretions and immunotherapy of
brain tumors.