Human Cd25+Cd4+ T Regulatory Cells Suppress Naive and Memory T Cell Proliferation and Can Be Expanded in Vitro without Loss of Function

MK Levings, R Sangregorio… - The Journal of …, 2001 - rupress.org
MK Levings, R Sangregorio, MG Roncarolo
The Journal of experimental medicine, 2001rupress.org
Active suppression by T regulatory (Tr) cells plays an important role in the downregulation of
T cell responses to foreign and self-antigens. Mouse CD4+ Tr cells that express CD25
possess remarkable suppressive activity in vitro and in autoimmune disease models in vivo.
Thus far, the existence of a similar subset of CD25+ CD4+ Tr cells in humans has not been
reported. Here we show that human CD25+ CD4+ Tr cells isolated from peripheral blood
failed to proliferate and displayed reduced expression of CD40 ligand (CD40L), in response …
Active suppression by T regulatory (Tr) cells plays an important role in the downregulation of T cell responses to foreign and self-antigens. Mouse CD4+ Tr cells that express CD25 possess remarkable suppressive activity in vitro and in autoimmune disease models in vivo. Thus far, the existence of a similar subset of CD25+CD4+ Tr cells in humans has not been reported. Here we show that human CD25+CD4+ Tr cells isolated from peripheral blood failed to proliferate and displayed reduced expression of CD40 ligand (CD40L), in response to T cell receptor–mediated polyclonal activation, but strongly upregulated cytotoxic T lymphocyte–associated antigen (CTLA)-4. Human CD25+CD4+ Tr cells also did not proliferate in response to allogeneic antigen-presenting cells, but they produced interleukin (IL)-10, transforming growth factor (TGF)-β, low levels of interferon (IFN)-γ, and no IL-4 or IL-2. Importantly, CD25+CD4+ Tr cells strongly inhibited the proliferative responses of both naive and memory CD4+ T cells to alloantigens, but neither IL-10, TGF-β, nor CTLA-4 seemed to be directly required for their suppressive effects. CD25+CD4+ Tr cells could be expanded in vitro in the presence of IL-2 and allogeneic feeder cells and maintained their suppressive capacities. These findings that CD25+CD4+ Tr cells with immunosuppressive effects can be isolated from peripheral blood and expanded in vitro without loss of function represent a major advance towards the therapeutic use of these cells in T cell–mediated diseases.
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