Increased Thrombin‐Activatable Fibrinolysis Inhibitor in Response to Sublingual Immunotherapy for Allergic Rhinitis. (12th April 2021)

• Record Type: Journal Article
• Authors: Yoshida, Kanako; Takabayashi, Tetsuji; Imoto, Yoshimasa; Sakashita, Masafumi; Kato, Yukinori; Narita, Norihiko; Fujieda, Shigeharu
• Is Part Of: Laryngoscope. Volume 131:Number 11(2021)
• Page Start: 2413
• Page End: 2420
• Publication Date: 2021-04-12
• Subjects: Allergic rhinitis -- sublingual immunotherapy -- anaphylatoxin C3a and C5a -- thrombin‐activatable fibrinolysis inhibitor; Otolaryngology -- Periodicals; 617.51005
• DOI: 10.1002/lary.29563
• Languages: English
• ISSNs: 0023-852X

Abstract

Abstract : Objectives/Hypothesis: The objective of this study was to determine the role of thrombin‐activatable fibrinolysis inhibitor (TAFI) as a candidate biomarker for therapeutic efficacy of sublingual immunotherapy (SLIT) and to identify the role of TAFI in the pathogenesis of allergic rhinitis (AR). Study Design: Retrospective cohort study and laboratory study. Methods: Serum was collected from patients with allergies to Japanese cedar pollen before, during, and after treatment with SLIT. We measured the levels of immunoreactive TAFI, C3a, and C5a in serum by enzyme‐linked immunosorbent assay (ELISA) and assessed their relative impact on a combined symptom‐medication score. We also examined the impact of TAFI on mast cells and fibroblasts in experiments performed in vitro. Results: Serum levels of TAFI increased significantly in response to SLIT. By contrast, serum C3a levels decreased significantly over time; we observed a significant negative correlation between serum levels of TAFI versus C3a and symptom‐medication score. Mast cell degranulation was inhibited in response to TAFI, as it was the expression of both CCL11 and CCL5 in cultured fibroblasts. Conclusions: High serum levels of TAFI may be induced by SLIT. TAFI may play a critical protective role in pathogenesis of AR by inactivating C3a and by inhibiting mast cell degranulation and chemokines expression in fibroblasts. Level of Evidence: 4 Laryngoscope, 131:2413–2420, 2021