Responsiveness of Naive CD4 T Cells to Polarizing Cytokine Determines the Ratio of Th1 and Th2 Cell Differentiation

Natallia Mikhalkevich(University of Rochester), Brian Becknell(The Ohio State University), Michael A. Caligiuri(The Ohio State University), Michael D. Bates(Cincinnati Children's Hospital Medical Center), Richard P. Harvey(Victor Chang Cardiac Research Institute), Wei-ping Zheng(University of Rochester)
The Journal of Immunology
February 1, 2006
Cited by 39Open Access
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Abstract

The intrinsic features of naive CD4 T cells that affect their ability to respond to polarizing signals for Th cell differentiation are not well understood. In this study, we show that naive CD4 T cells from mice transgenic for the Hlx gene expressed lower levels of IL-4Ralpha. The down-regulation of IL-4Ralpha diminished IL-4 signaling and the Th2 response and enhanced the Th1 response under suboptimal polarizing conditions. In nontransgenic CD4 T cells, blocking IL-4Ralpha with Abs had the same effect in an Ab dose-dependent manner. Conversely, Hlx haploinsufficiency caused higher expression of IL-4Ralpha to favor Th2 cell differentiation. Thus, the IL-4Ralpha level on naive CD4 T cells is genetically controlled by Hlx and determines the ratio of Th1 and Th2 cell differentiation.


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