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Instituto Gulbenkian de Ciência, Oeiras, Portugal; and
Centro de Inmunología Molecular, Habana, Cuba
Aiming to further our understanding of T cell-mediated suppression,
we investigate the plausibility of the hypothesis that regulatory T
cells suppress other T cells (target cells), while both cells are
conjugated with one APC. We use a mathematical model to analyze the
proliferation inhibition scored during in vitro suppression assays.
This model is a radical simplification of cell culture reality,
assuming that thymidine incorporation is proportional to the number of
target cells that would instantaneously form conjugates with APCs that
are free of regulatory cells. According to this model the inhibition
index should be mainly determined by the number of regulatory cells per
APC and should be insensitive to the number of target cells. We
reanalyzed several published data sets, confirming this expectation.
Furthermore, we demonstrate that the instantaneous inhibition index has
an absolute limit as a function of the number of regulatory cells per
APC. By calculating this limit we find that the model can explain the
data under two non-mutually exclusive conditions. First, only
15%
of APCs used in the suppression assays form conjugates with T cells.
Second, the growth of the regulatory cell population depends on the
target cells, such that the number of regulatory cells per APC
increases when they are cocultured with target cells and overcomes its
limit. However, if neither of these testable conditions is fulfilled,
then one could conclude that suppression in vitro does not require the
formation of multicellular conjugates.
This article has been cited by other articles:
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W. W. J. Unger, F. Hauet-Broere, W. Jansen, L. A. van Berkel, G. Kraal, and J. N. Samsom Early Events in Peripheral Regulatory T Cell Induction via the Nasal Mucosa J. Immunol., November 1, 2003; 171(9): 4592 - 4603. [Abstract] [Full Text] [PDF] |
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