ILC2 Regulatory Context Source Review Notes
Scope
This audit records a focused source-review pass for 10 previously provisional sources that refine ILC2 regulation, tissue-boundary interpretation, and asthma translation framing.
Sources Reviewed
- AHR cell-intrinsic restraint of intestinal ILC2s
- ILC2 regulatory network review
- tissue-specific ILC features
- ILC subset plasticity review
- RORalpha checkpoint for thymic T-cell versus ILC2 commitment
- metabolic features of ILCs review
- RXRgamma sets intestinal ILC2 activation threshold
- ADM2 promotes tissue-protective intestinal ILC2 responses
- tuft-cell IL-17RB restrains IL-25 bioavailability
- asthma immunotherapy review
Knowledge-Layer Changes
- Expanded ILC2 functional regulation mechanisms with AHR, RXRgamma, RORalpha, ADM2, tuft-cell IL-17RB/IL-25, metabolic-review, tissue-specific, plasticity, and asthma-immunotherapy framing.
- Updated ILC2, ILC2 roles in pulmonary disease, ILC in lung, and Lung ILC Core Evidence Synthesis.
- Review-level sources were kept as orientation layers rather than primary mechanistic anchors.
Boundary Rules
- Gut ILC2 AHR, RXRgamma, ADM2, and tuft-cell IL-17RB findings should remain gut-labeled unless direct pulmonary evidence is added.
- RORalpha thymic commitment evidence should be used for lineage-boundary framing, not mature lung disease regulation.
- Asthma immunotherapy review evidence should frame endotype-aware therapy logic but should not substitute for ILC-specific primary evidence.
Status
- Date: 2026-05-04
- Mode: focused manual crystallization
- Count: 10 source pages promoted from provisional to focused mode.