Group 2 innate lymphoid cells constrain type 3/17 lymphocytes in shared stromal niches to restrict liver fibrosis.
Julia Sbierski-KindKelly M CautivoJohanna C WagnerMadelene W DahlgrenJulia NilssonMaria KrasilnikovNicholas M MrozCarlos O LizamaAnna Lu GanPeri R MatatiaMarcela T TaruselliAnthony A ChangSofia CaryotakisClaire E O'LearyMaya KotasAras N MattisTien PengRichard M LocksleyAri B MolofskyPublished in: bioRxiv : the preprint server for biology (2023)
Group 2 innate lymphoid cells (ILC2s) cooperate with adaptive Th2 cells as key organizers of tissue type 2 immune responses, while a spectrum of innate and adaptive lymphocytes coordinate early type 3/17 immunity. Both type 2 and type 3/17 lymphocyte associated cytokines are linked to tissue fibrosis, but how their dynamic and spatial topographies may direct beneficial or pathologic organ remodelling is unclear. Here we used volumetric imaging in models of liver fibrosis, finding accumulation of periportal and fibrotic tract IL-5 + lymphocytes, predominantly ILC2s, in close proximity to expanded type 3/17 lymphocytes and IL-33 high niche fibroblasts. Ablation of IL-5 + lymphocytes worsened carbon tetrachloride-and bile duct ligation-induced liver fibrosis with increased niche IL-17A + type 3/17 lymphocytes, predominantly γδ T cells. In contrast, concurrent ablation of IL-5 + and IL-17A + lymphocytes reduced this progressive liver fibrosis, suggesting a cross-regulation of type 2 and type 3 lymphocytes at specialized fibroblast niches that tunes hepatic fibrosis.
Keyphrases
- liver fibrosis
- peripheral blood
- immune response
- multiple sclerosis
- bone marrow
- magnetic resonance
- atrial fibrillation
- dendritic cells
- rectal cancer
- radiation therapy
- endothelial cells
- cell proliferation
- neoadjuvant chemotherapy
- idiopathic pulmonary fibrosis
- lymph node
- oxidative stress
- drug induced
- computed tomography
- palliative care
- toll like receptor
- liver injury
- radiofrequency ablation
- extracellular matrix
- endoplasmic reticulum stress