Garcia Zacarias, Pradelli Emmanuelle, Celli Susanna, Beuneu Hélène, Simon Aurélie, Bousso Philippe
Institut Pasteur, G5 Dynamiques des Réponses Immunes, F-75015 Paris, France.
Proc Natl Acad Sci U S A. 2007 Mar 13;104(11):4553-8. doi: 10.1073/pnas.0610019104. Epub 2007 Mar 2.
The regulation of T cell-dendritic cell (DC) contacts during clonal expansion is poorly defined. Although optimal CD4 T cell responses require prolonged exposure to antigen (Ag), it is believed that stable T cell-DC interactions occur only during the first day of the activation process. Here we show that recently activated CD4 T cells are in fact fully competent for establishing contact with Ag-bearing DC. Using two-photon imaging, we found that whereas prolonged interactions between activated T cells and Ag-bearing DCs were infrequent at high T cell precursor frequency, they were readily observed for a period of at least 2 days when lower numbers of T cells were used. We provide evidence that, when present in high numbers, Ag-specific T cells still gained access to the DC surface but were competing for the limited number of sites on DCs with sufficient peptide-MHC complexes for the establishment of a long-lived interaction. Consistent with these findings, we showed that restoration of peptide-MHC level on DCs at late time points was sufficient to recover interactions between activated T cells and DCs. Thus, the period during which CD4 T cells continue to establish stable interactions with DCs is longer than previously thought, and its duration is dictated by both Ag levels and T cell numbers, providing a feedback mechanism for the termination of CD4 T cell responses.
在克隆扩增过程中,T细胞与树突状细胞(DC)接触的调节机制尚不清楚。尽管最佳的CD4 T细胞反应需要长时间暴露于抗原(Ag),但人们认为稳定的T细胞-DC相互作用仅发生在激活过程的第一天。在这里,我们表明最近激活的CD4 T细胞实际上完全有能力与携带Ag的DC建立接触。使用双光子成像,我们发现,在高T细胞前体频率下,激活的T细胞与携带Ag的DC之间的长时间相互作用很少见,但当使用较少数量的T细胞时,在至少2天的时间内很容易观察到这种相互作用。我们提供的证据表明,当大量存在时,Ag特异性T细胞仍然能够接触到DC表面,但它们正在与DC上有限数量的具有足够肽-MHC复合物的位点竞争,以建立长期相互作用。与这些发现一致,我们表明在后期恢复DC上的肽-MHC水平足以恢复激活的T细胞与DC之间的相互作用。因此,CD4 T细胞与DC持续建立稳定相互作用的时间比以前认为的要长,其持续时间由Ag水平和T细胞数量决定,这为CD4 T细胞反应的终止提供了一种反馈机制。