Department of Applied Biological Chemistry, The University of Tokyo, 1-1-1, Yayoj, Bunkyoku, Tokyo, 113-8657, Japan.
Cytotechnology. 2003 Nov;43(1-3):73-80. doi: 10.1023/b:cyto.0000039918.80472.0e.
Oral tolerance is the systemic immunological unresponsiveness that occurs after feeding protein antigens. Its physiological role is thought to be the prevention of hypersensitivity to food antigens, and its therapeutic use to treat inflammatory diseases has been suggested. Although it has been shown that CD4(+) T cells mediate oral tolerance, the precise molecular mechanisms remain unclear. In the present study, we employed suppression subtractive hybridization and identified 10 genes specifically expressed in orally tolerized T cells. These included genes that were interesting in terms of their putative functions in the negative regulation of T cell activation, e.g. Culin 1, LAX, and Zfhx1b, as well as four genes that encoded unknown proteins. We further investigated the expression of these genes in hyporesponsive T cells induced in vitro (in vitro anergized T cells). We found that six of the 10 genes were highly expressed in these cells, and kinetic studies suggested that one was associated with the induction of anergy, while the other five were associated with the maintenance of anergy. The remaining 4 genes that were not expressed in in vitro anergized T cells are also of interest as they may play a specific role in in vivo T cell tolerance. Functional analysis of these genes should help to understand the complex mechanisms underlying the induction and maintenance of oral tolerance, and moreover, in vivo immune tolerance in general.
口服耐受是在摄入蛋白抗原后发生的系统性免疫无应答。其生理作用被认为是预防对食物抗原的过敏反应,其治疗炎症性疾病的应用也已被提出。尽管已经表明 CD4(+) T 细胞介导了口服耐受,但确切的分子机制仍不清楚。在本研究中,我们采用抑制性消减杂交技术,鉴定了 10 个在口服耐受 T 细胞中特异性表达的基因。这些基因包括在 T 细胞激活的负调控方面具有潜在功能的基因,如 Culin 1、LAX 和 Zfhx1b,以及四个编码未知蛋白的基因。我们进一步研究了这些基因在体外诱导的低反应性 T 细胞(体外失能 T 细胞)中的表达。我们发现,这 10 个基因中有 6 个在这些细胞中高表达,动力学研究表明,其中一个与失能的诱导有关,而另外五个与失能的维持有关。另外 4 个在体外失能 T 细胞中不表达的基因也很有趣,因为它们可能在体内 T 细胞耐受中发挥特定作用。对这些基因的功能分析应该有助于理解诱导和维持口服耐受的复杂机制,进而有助于理解一般的体内免疫耐受。