Haptens, such as drugs and other low molecular weight chemicals, becom
e immunogenic only upon binding to proteins. Among antibiotics, penici
llins are most commonly used for the treatment of bacterial infections
and constitute a typical example of allergy inducing drugs in humans.
Previous work on their immunologic properties focused mainly on the e
xamination of IgE-mediated hypersensitivity reactions; however, drug-s
pecific T cell reactions are also involved in causing a serious allerg
ic inflammatory response. This review will focus on the interaction be
tween antibiotic molecules and penicillin-specific T lymphocytes in hu
mans. Experimental data accumulated so far on the reactivity of T cell
s with penicillin G point to penicilloyl-modified, major histocompatib
ility complex-associated peptides as T cell epitopes. The recognition
specificity of the respective T cell receptors appears to be directed
at both the backbone and the specific side chain of penicillin. In con
trast, the sequence of the carrier peptides appears to contribute litt
le to the antigenic specificity, mainly as a holder for the haptenic d
eterminant. Finally, recent results demonstrating the capacity of peni
cillins to modulate, in vitro, the Th0/Th2 phenotype of established T
cell clones will be presented and discussed in relation to possible th
erapeutic applications.