DX5+CD4+ T cells modulate cytokine production by CD4+ T cells towards IL‐10 via the production of IL‐4

• Published in: European journal of immunology 2010-10, Vol.40 (10), p.2731-2740
• Main Authors: Han, Wanda G. H., van der Voort, Ellen I. H., el Bannoudi, Hanane, Louis‐Plence, Pascale, Huizinga, Tom W. J., Toes, René E. M.
• Format: Article
• Language: English
• Subjects: Adaptive Immunity - immunology; Animals; CD4-Positive T-Lymphocytes - immunology; Cell Line; Cell Proliferation; Cellular immune response; Flow Cytometry; Immune regulation; Interferon-gamma - biosynthesis; Interferon-gamma - immunology; Interleukin-10 - immunology; Interleukin-4 - biosynthesis; Interleukin-4 - immunology; Mice; Mice, Inbred C57BL; Mice, Transgenic; Receptors, Antigen, T-Cell - immunology; T cells
• ISSN: 0014-2980; 1521-4141
• DOI: 10.1002/eji.201040574

CD4+ Th cells play a critical role in orchestrating the adaptive immune response. Uncontrolled Th1 responses are implicated in the pathogenesis of autoimmune diseases. T cells with immune‐modulatory properties are beneficial for inhibiting such inflammatory responses. Previously we demonstrated that repetitive injections of immature DC induce expansion of DX5+CD4+ T cells, which upon adoptive transfer show potent regulatory properties in murine collagen‐induced arthritis as well as in delayed‐hypersensitivity models. However, their regulatory mechanism remains to be defined. Here, we analyzed the effect of DX5+CD4+ T cells on other CD4+ T cells in vitro. Although proliferation of naïve CD4+ T cells upon antigenic triggering was not altered in the presence of DX5+CD4+ T cells, there was a striking difference in cytokine production. In the presence of DX5+CD4+ T cells, an IL‐10‐producing CD4+ T‐cell response was induced instead of a predominant IFN‐γ‐producing Th1 response. This modulation did not require cell–cell contact. Instead, IL‐4 produced by DX5+CD4+ T cells was primarily involved in the inhibition of IFN‐γ and promotion of IL‐10 production by CD4+ T cells. Together, our data indicate that DX5+CD4+ T cells modulate the outcome of Th‐responses by diverting Th1‐induction into Th responses characterized by the production of IL‐10.