In vitro analyses have shown anti-HIV immunotoxins to be among the mos
t effective AIDS antivirals tested. Because HIV has been continually s
elected by antibody, immunotoxins targeted to constant domains of vira
l antigens may not elicit drug-resistant mutants. A clinical trial wit
h CD4-PE40, a possibly flawed immunotoxin with nonspecific toxicity an
d short serum half-life, has reduced interest in this form of therapy.
It is proposed that the use of an immunotoxin directed against gp41 i
n combination with a CD4-Ig chimera is more likely to have a therapeut
ic effect than CD4-PE40. Clinical trials are also underway utilizing a
n immunotoxin that eliminates activated T-cells, an important cellular
locus of HIV-replication.