CD28 costimulation accelerates IL-4 receptor sensitivity and IL-4-mediatedTh2 differentiation

Citation
M. Kubo et al., CD28 costimulation accelerates IL-4 receptor sensitivity and IL-4-mediatedTh2 differentiation, J IMMUNOL, 163(5), 1999, pp. 2432-2442
Citations number
49
Categorie Soggetti
Immunology
Journal title
JOURNAL OF IMMUNOLOGY
ISSN journal
00221767 → ACNP
Volume
163
Issue
5
Year of publication
1999
Pages
2432 - 2442
Database
ISI
SICI code
0022-1767(19990901)163:5<2432:CCAIRS>2.0.ZU;2-H
Abstract
The development of Th1 and Th2 cells is determined by the type of antigenic stimulation involved in the initial cell activation step, Evidence indicat es that costimulatory signals, such as those delivered by CD28, play an imp ortant role in Th2 development, but little is known about how CD28 costimul ation contributes to Th2 development. In this study, TCR cross-linking was insufficient for Th2 development, while the addition of CD28 costimulation drastically increased Th2 generation through the IL-4-mediated pathway. Th2 generation following CD28 costimulation was not simply explained by the en hancement of IL-4 production in naive T cells. To generate Th2 cells after TCR cross-linking only, it was necessary to add a 20- to 200-fold excess of IL-4 generated after TCR and CD28 stimulation, TCR cross-linking increased the expression level and binding property of the IL-4R, but enhanced the s ensitivity to IL-4 only slightly. In contrast, as evidenced by the enhanced phosphorylation of Jak3, the IL-4R alpha-chain, and STAT6 following IL-4 s timulation, CD28 costimulation increased IL-4R sensitivity without affectin g its expression and binding property. This evidence of the enhancement of IL-4R sensitivity increases our understanding of how CD28 costimulation acc elerates Th2 development.