| First Author | Koliesnik IO | Year | 2019 |
| Journal | Immunobiology | Volume | 224 |
| Issue | 5 | Pages | 687-696 |
| PubMed ID | 31200979 | Mgi Jnum | J:317405 |
| Mgi Id | MGI:6852765 | Doi | 10.1016/j.imbio.2019.06.001 |
| Citation | Koliesnik IO, et al. (2019) Alternative NF-kappaB signaling controls peripheral homeostasis and function of regulatory T cells. Immunobiology 224(5):687-696 |
| abstractText | Regulatory T cells (Tregs) maintain immune homeostasis and play an important role in tissue regeneration after injury. Mutations affecting development or homeostasis of Tregs lead to immune pathologies in humans and are often fatal in mouse models. Although the pathways required for Treg development are being increasingly characterized, factors crucial for Treg homeostasis are not completely understood. Previously we have found a role for alternative NF-kappaB pathway in restricting T cell activation and Th17 differentiation. Here, by using the mouse model of uncontrolled alternative NF-kappaB signaling we identify a crucial intrinsic role of RelB signaling in regulating homeostasis and competitive fitness of Tregs. The failure of p100(-/-) Tregs to maintain the population of effector Tregs and efficiently suppress immune reactions results in lethal multiorgan Th1-mediated inflammation in Rag1(-/-) recipients. This inflammation is combined with severe lymphopenia and could be rescued by adoptive transfer of wild type Tregs. Thus in addition to its role in Th17 differentiation, RelB acts as a potent inhibitor of Treg effector functions. Our results point to RelB as a potential therapeutic target for Treg manipulation. |
