Background: It is well recognized that CD8 T cells inhibit IgE responses. I
n this study, we investigated the mechanism of CD8 T cell-mediated IgE supp
ression 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-C
D28 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 followin
g immunization with 100 mug of OVA/alum, serum IgE antibodies were measured
by passive cutaneous anaphylaxis and expressed as the highest dilution tha
t gave a detectable skin response. Results: Both Tc1 and Tc2 CD8 T cells fr
om OT-I mice inhibited IgE. Conclusion: Both Tc1 and Tc2 CD8 T cells promot
e Th1 immunity and inhibit IgE responses. This process appears to be indepe
ndent of CD8 T cell-derived IFN-gamma, as both Tc2 (IFN-gamma-) and Tc1 (IF
N-gamma+) CD8 T cells inhibited IgE. Copyright (C) 2001 S. Karger AG, Basel
.