A subclass of dendritic cells regulates the response of naive CD8 T cells by limiting their IL-2 production.

V Kronin, K Winkel, G Süss, A Kelso… - … (Baltimore, Md.: 1950 …, 1996 - journals.aai.org
V Kronin, K Winkel, G Süss, A Kelso, W Heath, J Kirberg, H von Boehmer, K Shortman
Journal of immunology (Baltimore, Md.: 1950), 1996journals.aai.org
Previous work indicated that a subclass of mouse spleen dendritic cells (DC), those bearing
CD8alpha, expresses the Fas ligand and restricts peripheral CD4 T cell responses by
initiating Fas-mediated apoptosis. To determine whether a similar regulation applies to CD8
T cells, they were purified from normal or from TCR-transgenic mice, and then cultured with
purified splenic CD8+ DC or CD8-DC presenting either alloantigens or the specific Ag for
the TCR transgene. In all systems studied, the proliferative response of CD8 T cells was …
Abstract
Previous work indicated that a subclass of mouse spleen dendritic cells (DC), those bearing CD8alpha, expresses the Fas ligand and restricts peripheral CD4 T cell responses by initiating Fas-mediated apoptosis. To determine whether a similar regulation applies to CD8 T cells, they were purified from normal or from TCR-transgenic mice, and then cultured with purified splenic CD8+ DC or CD8- DC presenting either alloantigens or the specific Ag for the TCR transgene. In all systems studied, the proliferative response of CD8 T cells was markedly less on stimulation with CD8+ DC compared with conventional CD8- DC. However, the basis of this restricted proliferation in response to CD8+ DC was totally different for CD8 T cells than for CD4 T cells. The reduced proliferation of CD8 T cells occurred later in the response than with CD4 T cells. In contrast with CD4 T cells, the reduced proliferation of CD8 T cells occurred even with T cells from Fas-deficient Ipr mice, or with DC from Fas ligand-deficient gld mice, indicating that Fas-induced apoptosis was not involved. Also, in contrast with CD4 T cells, the reduced proliferation of CD8 T cells was completely reversed by the addition of exogenous IL-2. Furthermore, cultures of CD8 T cells with CD8+ DC were found to be deficient in IL-2 production. Accordingly, although CD8+ DC are very efficient at stimulating CD8 T cells into cell division, they are deficient at stimulating endogenous cytokine production. The implications of these different DC regulatory systems are discussed.
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