Site-specific regulation of Th2 differentiation within lymph node microenvironments.
Miranda R Lyons-CohenElya A ShamskhouMichael Y GernerPublished in: The Journal of experimental medicine (2024)
T helper 2 (Th2) responses protect against pathogens while also driving allergic inflammation, yet how large-scale Th2 responses are generated in tissue context remains unclear. Here, we used quantitative imaging to investigate early Th2 differentiation within lymph nodes (LNs) following cutaneous allergen administration. Contrary to current models, we observed extensive activation and "macro-clustering" of early Th2 cells with migratory type-2 dendritic cells (cDC2s), generating specialized Th2-promoting microenvironments. Macro-clustering was integrin-mediated and promoted localized cytokine exchange among T cells to reinforce differentiation, which contrasted the behavior during Th1 responses. Unexpectedly, formation of Th2 macro-clusters was dependent on the site of skin sensitization. Differences between sites were driven by divergent activation states of migratory cDC2 from different dermal tissues, with enhanced costimulatory molecule expression by cDC2 in Th2-generating LNs promoting prolonged T cell activation, macro-clustering, and cytokine sensing. Thus, the generation of dedicated Th2 priming microenvironments through enhanced costimulatory molecule signaling initiates Th2 responses in vivo and occurs in a skin site-specific manner.
Keyphrases
- lymph node
- dendritic cells
- single cell
- high resolution
- cell cycle
- rna seq
- induced apoptosis
- poor prognosis
- wound healing
- oxidative stress
- neoadjuvant chemotherapy
- regulatory t cells
- gene expression
- sentinel lymph node
- immune response
- squamous cell carcinoma
- soft tissue
- palliative care
- cell proliferation
- cell cycle arrest
- mass spectrometry
- radiation therapy
- allergic rhinitis
- binding protein
- cell adhesion