Abstract
Background: It is well recognized that CD8 T cells inhibit IgE responses. In this study, we investigated the mechanism of CD8 T cell-mediated IgE suppression by comparing the capacity of T cytotoxic 1 (Tc1) and T cytotoxic 2 (Tc2) CD8 T cells to inhibit IgE responses to ovalbumin (OVA). Methods: Tc1 and Tc2 CD8 T cells were generated from OVA(257-264)-specific V beta5.2 T cell receptor (TcR) transgenic mice by stimulation with anti-CDS and anti-CD28 under Tc1 and Tc2 polarizing conditions. Tc1 and Tc2 V beta5.2 TcR CD8 T cells (10(6)) were adoptively transferred to syngeneic mice, and following immunization with 100 mug of OVA/alum, serum IgE antibodies were measured by passive cutaneous anaphylaxis and expressed as the highest dilution that gave a detectable skin response. Results: Both Tc1 and Tc2 CD8 T cells from OT-I mice inhibited IgE. Conclusion: Both Tc1 and Tc2 CD8 T cells promote Th1 immunity and inhibit IgE responses. This process appears to be independent of CD8 T cell-derived IFN-gamma, as both Tc2 (IFN-gamma-) and Tc1 (IFN-gamma+) CD8 T cells inhibited IgE. Copyright (C) 2001 S. Karger AG, Basel.
Original language | English |
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Pages (from-to) | 187 - 189 |
Number of pages | 3 |
Journal | International Archives of Allergy and Immunology |
Volume | 124 |
Issue number | 1-3 |
Publication status | Published - 2001 |
Event | 23rd Symposium of the Collegium Internationale Allergologicum (CIA 2000) - HAKONE, Japan Duration: 1 Jan 2001 → … |