Raimondi Giorgio, Zanoni Ivan, Citterio Stefania, Ricciardi-Castagnoli Paola, Granucci Francesca
Department of Biotechnology and Bioscience, University of Milano-Bicocca, Milan, Italy.
J Immunol. 2006 Apr 1;176(7):4021-8. doi: 10.4049/jimmunol.176.7.4021.
Ag presentation in the absence of danger signals and Ag persistence are the inductive processes of peripheral T cell tolerization proposed so far. Nevertheless, it has never been definitively shown that chronic Ag presentation per se can induce T cell tolerance independent of the state of activation of APCs. In the present work, we investigated whether chronic Ag presentation by either resting or activated B cells can induce tolerance of peripheral Ag-specific T cells. We show that CD4(+) T cells that re-encounter the Ag for a prolonged period, presented either by resting or activated Ag-presenting B cells, become nonfunctional and lose any autoimmune reactivity. Thus, when the main APCs are B cells, the major mechanism responsible for peripheral T cell tolerization is persistent Ag exposure, independent of the B cell activation state.
在缺乏危险信号的情况下抗原呈递以及抗原持续存在是目前所提出的外周T细胞耐受的诱导过程。然而,从未有确凿证据表明慢性抗原呈递本身能够独立于抗原呈递细胞(APC)的激活状态而诱导T细胞耐受。在本研究中,我们调查了静息或活化的B细胞进行慢性抗原呈递是否能够诱导外周抗原特异性T细胞产生耐受。我们发现,长时间再次接触由静息或活化的抗原呈递B细胞所呈递抗原的CD4(+) T细胞会失去功能,并丧失任何自身免疫反应性。因此,当主要的抗原呈递细胞为B细胞时,外周T细胞耐受的主要机制是持续的抗原暴露,而与B细胞的激活状态无关。