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The fact that cerebrolysin, which promotes angiogenesis through VEGF upregulation, shows benefit in this specific condition aligns with its known mechanisms

BBR dose-dependently inhibited IgE reduction in a non-cytotoxic manner (nearly 100% at 5 g/mL) and at 5 g/mL, inhibited X box binding protein 1 (XBP1), B-lymphocyte-induced maturation protein 1 (BLIMP1), and STAT6 suppression, and reduced mitochondrial oxidation rate of IgE-producing plasma cells in vitro (Fig