Gamma/delta T cells from tolerized alpha/beta-TCR-deficient mice antigen specifically inhibit contact sensitivity in vivo and IFN-gamma production in vitro.
Gamma/delta T cells from tolerized alpha/beta-TCR-deficient mice antigen specifically inhibit contact sensitivity in vivo and IFN-gamma production in vitro.
复制标题
来自耐受的 α/β-TCR 缺陷小鼠抗原的 γ/δ T 细胞特异性抑制体内接触敏感性和体外 IFN-γ 产生。
DOI:
10.1159/000237607
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发表时间:
1997
影响因子:
2.8
通讯作者:
Askenase,PW
中科院分区:
文献类型:
--
作者:
Szczepanik,M;Anderson,LR;Ushio,H;Ptak,W;Owen,MJ;Hayday,AC;Askenase,PW
Contact sensitivity (CS) responses to reactive hapten antigens (Ag), such as picryl chloride, are classical examples of T-cell-mediated immune responses in vivo. There is also abundant evidence that T cells exposed in vivo to high intravenous doses of Ag can downregulate CS (high-dose Ag tolerance). To clarify cell types that effect CS and mediate its downregulation, we have studied CS in mice congenitally deficient in α/β T cells (α-/- mice). We show that α-7- mice cannot mount CS, implicating α/β T cells as critical CS effector cells. However, after high-dose Ag tolerization, these α-7- mice can downregulate α/β CS effector cells adoptively transferred to them. The active cells in tolerized α-/- mice are γ/δ TCR+ cells which downregulate CS effector α/β T cells Ag-specifically upon adoptive cell transfer. Moreover, γ/δ cells can Ag-specifícally downregulate IFN-γ production by CS effector cells in vitro. These findings establish that γ/δ T cells are not CS effector cells but downregulate CS, in agreement with recent reports that γ/δ T cells downregulate IgE responses.