The Journal of Experimental Medicine · 2000 · 1.5K citations · 35 references
Life SciencesCell BiologyImmunologyAdaptive ImmunityCellular ImmunologyImmunoregulationCell-mediated ImmunityImmune Cell DifferentiationImmune MaturationT Cell ActivationT Cell BiologyT Cell DifferentiationAlloreactive T Cell RegulationAlloreactive T Cell ResponsesCd4 Positive T CellsInterferon Gamma ProductionT Cell Priming By Dendritic CellsT Helper 1 DifferentiationT Helper Cell DevelopmentT Helper Cells
The functional properties of dendritic cells (DCs) are strictly dependent on their maturational state. The study examined how immature versus mature DCs prime naive allogeneic CD4⁺ T cells, using CD83⁻ and CD83⁺ DCs to assess T‑cell priming and differentiation. Repeated stimulation with mature DCs expanded alloreactive T cells into Th1 cells, whereas stimulation with immature DCs irreversibly halted proliferation, induced CTLA‑4, suppressed cytokine production, and differentiated the cells into nonproliferating IL‑10‑producing regulatory T cells that potently inhibited antigen‑driven Th1 proliferation in a contact‑ and dose‑dependent, antigen‑non‑specific manner.
The functional properties of dendritic cells (DCs) are strictly dependent on their maturational state. To analyze the influence of the maturational state of DCs on priming and differentiation of T cells, immature CD83(-) and mature CD83(+) human DCs were used for stimulation of naive, allogeneic CD4(+) T cells. Repetitive stimulation with mature DCs resulted in a strong expansion of alloreactive T cells and the exclusive development of T helper type 1 (Th1) cells. In contrast, after repetitive stimulation with immature DCs the alloreactive T cells showed an irreversibly inhibited proliferation that could not be restored by restimulation with mature DCs or peripheral blood mononuclear cells, or by the addition of interleukin (IL)-2. Only stimulation of T cells with mature DCs resulted in an upregulation of CD154, CD69, and CD70, whereas T cells activated with immature DCs showed an early upregulation of the negative regulator cytotoxic T lymphocyte-associated molecule 4 (CTLA-4). These T cells lost their ability to produce interferon gamma, IL-2, or IL-4 after several stimulations with immature DCs and differentiated into nonproliferating, IL-10-producing T cells. Furthermore, in coculture experiments these T cells inhibited the antigen-driven proliferation of Th1 cells in a contact- and dose-dependent, but antigen-nonspecific manner. These data show that immature and mature DCs induce different types of T cell responses: inflammatory Th1 cells are induced by mature DCs, and IL-10-producing T cell regulatory 1-like cells by immature DCs.
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Jung‐Hyun Park, Stanley Adoro, Terry I. Guinter et al. · Nature Immunology · 2010 · 5.8K citations · Full text
Shimon Sakaguchi, N Sakaguchi, M Asano et al. · The Journal of Immunology · 1995 · 5.5K citations
Life Sciences, Immunology, Pathology +17
A CD4+T-cell subset inhibits antigen-specific T-cell responses and prevents colitis
Hervé Groux, Anne O’Garra, Mike Bigler et al. · Nature · 1997 · 3.6K citations
Life Sciences, Immunology, Pathology +12