Microbiota-induced tertiary lymphoid tissues aggravate inflammatory disease in the absence of ROR gamma t and LTi cells

作者：Lochner Matthias; Ohnmacht Caspar; Presley Laura; Bruhns Pierre; Si Tahar Mustapha; Sawa Shinichiro; Eberl Gerard^*

来源：Journal of Experimental Medicine, 2011, 208(1): 125-134.

DOI：10.1084/jem.20100052

The programmed development of lymph nodes and Peyer's patches during ontogeny requires lymphoid tissue inducer (LTi) cells that express the nuclear hormone receptor ROR gamma t. After birth, LTi cells in the intestine cluster into cryptopatches, the precursors of isolated lymphoid follicles (ILFs), which are induced to form by symbiotic bacteria and maintain intestinal homeostasis. We show that in ROR gamma t-deficient mice, which lack LTi cells, programmed lymphoid tissues, ILFs, and Th17 cells, bacterial containment requires the generation of large numbers of tertiary lymphoid tissues (tLTs) through the activity of B cells. However, upon epithelial damage, these mice develop severe intestinal inflammation characterized by extensive recruitment of neutrophils and IgG(+) B cells, high expression of activation-induced deaminase in tLTs, and wasting disease. The pathology was prevented by antibiotic treatment or inhibition of lymphoid tissue formation and was significantly decreased by treatment with intravenous immunoglobulin G (IVIG). Our data show that intestinal immunodeficiency, such as an absence in ROR gamma t-mediated proinflammatory immunity, can be compensated by increased lymphoid tissue genesis. However, this comes at a high cost for the host and can lead to a deregulated B cell response and aggravated inflammatory pathology.

• 出版日期2011-1-17