The feasibility to raise nonhuman primate antibodies against selected
components of the human immune system was tested. The immunogens were
whole cells (human T lymphocytes) or purified, recombinant human prote
ins (cytokines: TNF alpha or GM-CSF soluble forms of cell surface anti
gens: sCD4 or sCD25). Significant Immunizations, yielding functionally
relevant antibodies, were readily achieved in rhesus monkeys, but, no
t surprisingly, may be less frequent in chimpanzees. The results sugge
st a general strategy for production of therapeutically useful MAB.