| Article ID | Journal | Published Year | Pages | File Type |
|---|---|---|---|---|
| 2832817 | Molecular Immunology | 2008 | 10 Pages |
Human IL-4Rα binds to mouse γc resulting in a chimeric receptor specific for human IL-4 but not mouse IL-4, providing in principle an inducible hIL-4 system. We investigated the in vitro and in vivo characteristics of human IL-4Rα transgenic mice on a mouse IL-4Rα-deficient background (hIL-4Rα Tg/mIL-4Rα−/−). The integrity of lymphocyte-specific hIL-4Rα expression in hIL-4Rα Tg/mIL-4Rα−/− mice was demonstrated by FACS analysis. This was confirmed in functional studies as lymphocytes responded to recombinant hIL-4 but not mIL-4 or mIL-13 in proliferation and T helper differentiation assays, demonstrating species-specificity and inducibility of the chimeric receptor in vitro. We then infected transgenic mice with Nippostrongylus brasiliensis, known to induce a strong Type 2 response in wild-type mice. As expected hIL-4Rα Tg/mIL-4Rα−/− mice were unable to expel N. brasiliensis worms which confirms unresponsiveness in non-lymphocytes. However they developed a Th2 cytokine and IgE response in the absence of induction with hIL-4. These results suggested that lymphocyte-specific IL-4Rα responsiveness was still present in vivo. Neutralization of endogenous mIL-4 resulted in inhibition of N. brasiliensis-induced Th2 cytokine and total IgE production in hIL-4Rα Tg/mIL-4Rα−/− mice suggesting that mIL-4 was involved. Intercrossing hIL-4Rα Tg/mIL-4Rα−/− mice with mIL-4−/−/mIL-13−/− mice completely abrogated Type 2 responses in N. brasiliensis infections. Together, these data demonstrate that mIL-4 triggered the hIL-4Rα/mγc chimeric receptor in vivo.
