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Proinflammatory microenvironments within the intestine regulate the differentiation of tissue-resident CD8+ T cells responding to infection
Proinflammatory microenvironments within the intestine regulate the differentiation of tissue-resident CD8+ T cells responding to infection
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Proinflammatory microenvironments within the intestine regulate the differentiation of tissue-resident CD8+ T cells responding to infection
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Proinflammatory microenvironments within the intestine regulate the differentiation of tissue-resident CD8+ T cells responding to infection
Proinflammatory microenvironments within the intestine regulate the differentiation of tissue-resident CD8+ T cells responding to infection

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Proinflammatory microenvironments within the intestine regulate the differentiation of tissue-resident CD8+ T cells responding to infection
Proinflammatory microenvironments within the intestine regulate the differentiation of tissue-resident CD8+ T cells responding to infection
Journal Article

Proinflammatory microenvironments within the intestine regulate the differentiation of tissue-resident CD8+ T cells responding to infection

2015
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Overview
Tissue-resident memory T cells (T RM cells) provide rapid frontline protection from reinfection. Bergsbaken and Bevan identify a gut T RM cell population generated via an unconventional pathway that is protective against a natural mouse intestinal pathogen. We report that oral infection with Yersinia pseudotuberculosis results in the development of two distinct populations of pathogen-specific CD8 + tissue-resident memory T cells (T RM cells) in the lamina propria. CD103 − T cells did not require transforming growth factor-β (TGF-β) signaling but were true resident memory cells. Unlike CD103 + CD8 + T cells, which were TGF-β dependent and were scattered in the tissue, CD103 − CD8 + T cells clustered with CD4 + T cells and CX3CR1 + macrophages and/or dendritic cells around areas of bacterial infection. CXCR3-dependent recruitment of cells to inflamed areas was critical for development of the CD103 − population and pathogen clearance. Our studies have identified the 'preferential' development of CD103 − T RM cells in inflammatory microenvironments within the lamina propria and suggest that this subset has a critical role in controlling infection.
Publisher
Nature Publishing Group US,Nature Publishing Group