Monoclonal antibodies (Mabs) have long been considered a good class of
natural drugs, both because they mimic their natural role in the body
and because they have no inherent toxicity. Although rodent Mabs are
readily generated, their widespread use as therapeutic agents has been
hampered because they are recognized as foreign by the patient. Evide
ntly, clinical Mabs should be as human as possible and results with so
me of the more recently developed chimerized and humanized Mabs are te
stimony to this. Mabs that are entirely human are now being produced f
rom phage display and transgenic mice. The first fully human Mabs gene
rated by phage display have already entered clinical trials, and toget
her with recent advances in these technologies, may finally realize th
e full potential of antibodies.