AT1R (Angiotensin II Receptor Type 1) antibodies are immunoglobulins targeting the angiotensin II receptor type 1, a G-protein-coupled receptor critical for cardiovascular homeostasis. These antibodies can act as agonists or allosteric modulators, influencing blood pressure, fibrosis, and immune responses .
AT1R antibodies are implicated in systemic sclerosis (SSc), COVID-19, and cardiovascular diseases.
Systemic Sclerosis (SSc): AT1R antibodies induce skin/lung fibrosis, endothelial apoptosis, and inflammation in murine models. These effects depend on CD4+ T cells and B cells .
COVID-19: Elevated AT1R antibody titers (>17 U/mL) correlate with severe disease courses, though causality remains uncertain .
AT1R antibodies exhibit isotype-specific properties influencing binding affinity and effector functions:
| Isotype | Source | Applications | Key Features |
|---|---|---|---|
| IgG1 | Mouse/rat | ELISA, IHC, IP | High affinity, stable in denaturing conditions |
| IgG2a | Rat | Flow cytometry, in vivo models | Strong Fc-mediated ADCC |
| IgG2b | Mouse | Neutralizing assays | Intermediate Fc receptor binding |
Example: The AT1 Antibody (G-3) (IgG1 κ) detects AT1R in western blot (WB), immunoprecipitation (IP), and immunofluorescence (IF) .
Species Specificity: AT1R antibodies often cross-react with human, mouse, and rat AT1R isoforms (e.g., AT1R G-3 antibody) .
Assay Optimization: Conjugation with HRP or fluorescent tags (e.g., FITC, Alexa Fluor®) enables multiplex detection in ELISA or flow cytometry .
Variable Affinity: Allelic diversity in antibody constant regions (e.g., IGHG1, IGHG3) affects Fc receptor binding and serum persistence .
Immunogenicity: Non-allotypic mutations in Fc regions may alter therapeutic efficacy or provoke anti-drug antibodies .