Methodological Answer:
Use AT1R-immunized murine models: Inject C57BL/6J mice with membrane-embedded human AT1R to induce skin/lung inflammation and fibrosis .
Include T/B cell-deficient mice: Differentiate antibody-mediated effects from adaptive immune contributions (e.g., CD4+ T cell dependency) .
Apply monoclonal AT1R antibodies: Validate pathogenicity via passive transfer into wild-type vs. AT1R knockout mice .
Data Table: Specificity Challenges in Commercial AT1R Antibodies
Methodological Answer:
Stratify patients by AT1R antibody levels: In COVID-19, anti-AT1R positivity (≥10 U/mL) correlates with reduced hospitalization risk (14.86% positivity in patients vs. 29.46% in controls) .
Use competitive inhibition assays: Measure antibody interference with angiotensin II binding to assess protective vs. pathogenic roles .
Pair with cytokine profiling: Link AT1R antibody levels to IL-8 or TGF-β pathways in longitudinal cohorts .
Antibody Validation: Always include knockout controls and orthogonal assays .
Assay Selection: Prioritize functional assays (e.g., luminometric bioassays) over ELISA for clinical relevance .
Pathway Analysis: Combine AT1R antibody data with downstream markers (e.g., Smad2/3 phosphorylation in fibrosis models) .