Department of Pathology and Immunology, Washington University School of Medicine, 660 S. Euclid Avenue, Saint Louis, MO 63110, USA.
Department of Microbiology and Immunology, University of Michigan Medical School, 1500 E Medical Center Drive, Ann Arbor, MI 48109, USA.
Sci Immunol. 2019 Feb 8;4(32). doi: 10.1126/sciimmunol.aau9079.
T cell responses to symbionts in the intestine drive tolerance or inflammation depending on the genetic background of the host. These symbionts in the gut sense the available nutrients and adapt their metabolic programs to use these nutrients efficiently. Here, we ask whether diet can alter the expression of a bacterial antigen to modulate adaptive immune responses. We generated a CD4 T cell hybridoma, BθOM, specific for (). Adoptively transferred transgenic T cells expressing the BθOM TCR proliferated in the colon, colon-draining lymph node, and spleen in colonized healthy mice and differentiated into regulatory T cells (T) and effector T cells (T). Depletion of -specific T resulted in colitis, showing that a single protein expressed by can drive differentiation of T that self-regulate T to prevent disease. We found that BθOM T cells recognized a peptide derived from a single protein, BT4295, whose expression is regulated by nutrients, with glucose being a strong catabolite repressor. Mice fed a high-glucose diet had a greatly reduced activation of BθOM T cells in the colon. These studies establish that the immune response to specific bacterial antigens can be modified by changes in the diet by altering antigen expression in the microbe.
肠道共生体的 T 细胞反应会根据宿主的遗传背景导致耐受或炎症。这些肠道共生体会感知可用的营养物质,并调整其代谢程序以有效利用这些营养物质。在这里,我们想知道饮食是否可以改变细菌抗原的表达,从而调节适应性免疫反应。我们生成了一个针对 () 的 CD4 T 细胞杂交瘤 BθOM。表达 BθOM TCR 的转基因 T 细胞在定植健康小鼠的结肠、结肠引流淋巴结和脾脏中增殖,并分化为调节性 T 细胞 (Treg) 和效应 T 细胞 (Teff)。-特异性 T 细胞耗竭导致结肠炎,表明 表达的单个蛋白可驱动 Treg 的分化,以自调控 T 细胞来预防疾病。我们发现 BθOM T 细胞识别来自单个 蛋白 BT4295 的肽,其表达受营养物质调控,葡萄糖是强烈的分解代谢物抑制剂。高糖饮食的小鼠在结肠中 BθOM T 细胞的激活大大减少。这些研究表明,通过改变微生物中抗原的表达,饮食的变化可以改变对特定细菌抗原的免疫反应。