Abstract
It is known that vitamin A and its metabolite, retinoic acid (RA), are essential for host defense. However, the mechanisms for how RA controls inflammation are incompletely understood. The findings presented in this study show that RA signaling occurs concurrent with the development of inflammation. In models of vaccination and allogeneic graft rejection, whole body imaging reveals that RA signaling is temporally and spatially restricted to the site of inflammation. Conditional ablation of RA signaling in T cells significantly interferes with CD4+ T cell effector function, migration, and polarity. These findings provide a new perspective of the role of RA as a mediator directly controlling CD4+ T cell differentiation and immunity.
| Original language | English |
|---|---|
| Pages (from-to) | 1767-1775 |
| Number of pages | 9 |
| Journal | Journal of Experimental Medicine |
| Volume | 208 |
| Issue number | 9 |
| DOIs | |
| State | Published - 29 Aug 2011 |
| Externally published | Yes |
UN SDGs
This output contributes to the following UN Sustainable Development Goals (SDGs)
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SDG 3 Good Health and Well-being
Keywords
- Dendritic cells
- Vitamin-a
- Small-intestine
- Receptor-alpha
- Expressio
- Differentiation
- Generation
- Induction
- System
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