The present article describes procedures to measure rat IL-4 protein. The R
T-PCR technique has been successfully and widely used to measure IL-4 mRNA,
but it does not determine IL-4 protein synthesis. Assays to measure rat IL
-4 protein based on its biological activity were developed using the mAb OX
-81, which inhibits rat IL-4 activity. Two bioassays were attempted based o
n the ability of IL-4 to induce the proliferation of T cell blasts and to i
ncrease MHC class LI expression on resting B cells. A second mAb against ra
t IL-4 was used in a sandwich ELISA to detect rat IL-4. This ELISA is satis
factory although its sensitivity is not as high as that of the bioassay. Ac
cording to our experience, the bioassay based on the induction of class II
MHC molecules on B cells is the technique of choice for rat IL-4 determinat
ion because it proved specific, sensitive and reproducible. (C) 1998 Elsevi
er Science B.V. All rights reserved.