Interleukin-4 (IL-4) is currently being used for therapeutic intervent
ion in a wide range of malignant diseases as an antitumour agent. Alth
ough bioassays have been developed that measure the proliferative capa
city of IL-4, none measure the antiproliferative activity of this mole
cule. We have developed a simple, sensitive bioassay for human IL-4 ba
sed on the ability of this cytokine to inhibit the proliferation of th
e human lung carcinoma line, CCL-185, an easy to maintain, cytokine in
dependent, cell line. It is rapid, reproducible and sensitive, able to
detect 2 pg/ml IL-4. The assay is completely unresponsive to all othe
r interleukins from IL-2 to IL-12, to the colony stimulating factors a
nd transforming growth factor beta and is 100-fold less sensitive to i
nterferon-alpha, tumour necrosis factor-alpha, IL-1 beta and IL-13. Th
e assay can be made completely specific for IL-4 by including specific
neutralizing antibodies for IL-4 and is suitable for the estimation o
f IL-4 in both plasma and serum samples.