A series of rat monoclonal antibodies (MABs) has been generated agains
t the extracellular domain of the receptor for EGF which block the bin
ding of EGF and TGF alpha to the receptor and inhibit the growth in vi
tro of a range of carcinoma cell lines that over-express the receptor
for EGF. Some of these antibodies were able also to induce the complet
e regression of xenografts of EGFR-over-expressing tumours when treatm
ent was started, either at the time of tumour inoculation or later whe
n the tumours were established. The most effective of these antibodies
was ICR62, which was also able to activate host immune effector funct
ions. We conclude that antibodies which block growth-factor-ligand int
eraction can have a profound influence on the proliferative capacity o
f tumour cells in vivo and may have useful clinical application. (C) 1
994 Wiley-Liss, Inc.