Helft Julie, Jacquet Alexandra, Joncker Nathalie T, Grandjean Isabelle, Dorothée Guillaume, Kissenpfennig Adrien, Malissen Bernard, Matzinger Polly, Lantz Olivier
Laboratoire d'Immunologie Clinique, Inserm U653, Institut Curie, Paris.
Blood. 2008 Aug 15;112(4):1249-58. doi: 10.1182/blood-2007-09-114389. Epub 2008 Jun 6.
The regulation of CD4 T-cell numbers during an immune response should take account of the amount of antigen (Ag), the initial frequency of Ag-specific T cells, the mix of naive versus experienced cells, and (ideally) the diversity of the repertoire. Here we describe a novel mechanism of T-cell regulation that potentially deals with all of these parameters. We found that CD4 T cells establish a negative feedback loop by capturing their cognate major histocompatibility class (MHC)/peptide complexes from Ag-presenting cells and presenting them to Ag-experienced CD4 T cells, thereby inhibiting their recruitment into the response while allowing recruitment of naive T cells. The inhibition is Ag specific, begins at day 2 (long before Ag disappearance), and cannot be overcome by providing new Ag-loaded dendritic cells. In this way, CD4 T-cell proliferation is regulated in a functional relationship to the amount of Ag, while allowing naive T cells to generate repertoire variety.
免疫应答过程中CD4 T细胞数量的调节应考虑抗原(Ag)的量、Ag特异性T细胞的初始频率、幼稚细胞与记忆细胞的比例,以及(理想情况下)T细胞受体库的多样性。在此,我们描述了一种潜在涉及所有这些参数的T细胞调节新机制。我们发现,CD4 T细胞通过从抗原呈递细胞捕获其同源主要组织相容性复合体(MHC)/肽复合物,并将其呈递给已接触过Ag的CD4 T细胞,从而建立一个负反馈回路,进而抑制它们被招募进入应答反应,同时允许幼稚T细胞被招募。这种抑制是抗原特异性的,在第2天开始(远在抗原消失之前),并且不能通过提供新的负载抗原的树突状细胞来克服。通过这种方式,CD4 T细胞的增殖以与抗原量的功能关系进行调节,同时允许幼稚T细胞产生受体库多样性。