International Immunology, Vol. 5, No. 9, pp. 1041-1048,September 1993
© 1993 Japanese Society for Immunology
Synergistic interactions of CD4+ and CD8+ T cell subsets with human vascular endothelial cells in primary proliferative allogeneic responses
Vascular Biology Team, Section of Transplantation Biology, Clinical Research Centre Harrow HA1 3UJ, UK
Correspondence to: Correspondence to: C. O. S. Savage
The ability of subcultured human vascular endothelial cells (EC) to provide immune accessory functions for proliferative responses of highly purified allogeneic CD4+ and CD8+ T cells has been examined. CD4+ T cells proliferated in response to IFN-
-pretreated EC which expressed class II molecules, but not to untreated EC. CD8+ T cells proliferated to MHC class I molecules expressed on both untreated and IFN-
-treated EC. Combined populations of CD4+ and CD8+ T cells showed synergistic, rather than additive, responses to both untreated and IFN-
-treated EC. Furthermore, CD8+ T cells were able to induce MHC class II expression on endothelial cells and this induction could be inhibited by an anti-IFN-
mAb. The synergistic response obtained by co-culturing CD4+ and CD8+ T cells with vascular EC was completely inhibited by the sameantl-IFN-
mAb. These studies suggest that CD4+ and CD8+ T cells recognise and proliferate to allogeneic MHC molecules expressed by EC. CD4+ and CD8+responses are synergistic under the conditions tested and this synergism appears to be due to induction of MHC class II antigens on C by IFN-
secreted from CD8+ T cells.
Keywords: endothelial cells, interferon-
, major histocompatibility complex, peripheral blood lymphocytes
Received 12 January 1993, accepted 17 May 1993.
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