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Cooperation between Th1 and Th2 cells in a murine model of eosinophilic airway inflammation
David A. Randolph, … , Cynthia J.L. Carruthers, David D. Chaplin
David A. Randolph, … , Cynthia J.L. Carruthers, David D. Chaplin
Published October 15, 1999
Citation Information: J Clin Invest. 1999;104(8):1021-1029. https://doi.org/10.1172/JCI7631.
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Article

Cooperation between Th1 and Th2 cells in a murine model of eosinophilic airway inflammation

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Abstract

We have studied the actions of helper T lymphocyte-1 and -2 (Th1 and Th2) cells in an acute model of eosinophilic airway inflammation by infusing chicken ovalbumin-specific (OVA-specific) Th1 cells, Th2 cells, or both into unsensitized mice and challenging the mice with an OVA aerosol. OVA challenge after infusion of Th1 cells alone resulted in airway inflammation with lymphocytes and monocytes. Challenge after the infusion of Th2 cells alone resulted in minimal inflammation. In contrast, when Th1 and Th2 cells were transferred together, they cooperated to promote a robust eosinophil-predominant inflammatory response. Th1 cells alone were readily recruited to the airways after challenge, but in the absence of Th1 cells, Th2 cells did not accumulate in the airways. When transferred together, both Th1 and Th2 cells, as well as endogenous eosinophils, were effectively recruited. This recruitment was correlated with increased VCAM-1 expression in the medium- and large-sized vessels of the lung and could be inhibited by treating the mice with neutralizing antibodies to TNF-α or VCAM-1. These data indicate that Th2 cells require signals in addition to antigen for their effective recruitment to the airways. Th1 cells can provide these signals.

Authors

David A. Randolph, Robin Stephens, Cynthia J.L. Carruthers, David D. Chaplin

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Figure 3

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Flow cytometric analysis of Th1 and Th2 cell recruitment to the airways ...
Flow cytometric analysis of Th1 and Th2 cell recruitment to the airways after challenge. Groups of 4 mice received (a) no transferred cells, (b) 107 DO11.10 Th1 cells, (c) 107 DO11.10 Th2 cells, or (d) 5 × 106 Th1 cells plus 5 × 106 Th2 cells. The mice were challenged, and BAL cells were collected as described in Figure 1. Cells from each group were pooled and then stimulated for 6 hours with PMA and ionomycin in the presence of monensin. Aliquots were stained with anti-CD4 and the anti-clonotypic antibody KJ1-26 to mark the transferred transgenic T cells. The cells were then fixed, permeabilized, and stained for intracellular IFN-γ and IL-4 as markers for Th1 and Th2 differentiation before analysis by flow cytometry. IFN-γ and IL-4 staining are shown for cells within the CD4+ KJ1-26+ gate. The numbers of cytokine-producing Th1 (IFN-γ+ IL-4–) and Th2 (IFN-γ– IL-4+) cells are indicated. Similar results were seen in 3 separate experiments.

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