4.7 Article

Studies on activation and regulation of the coagulation cascade in chronic rhinosinusitis with nasal polyps

期刊

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MOSBY-ELSEVIER
DOI: 10.1016/j.jaci.2022.02.018

关键词

Chronic rhinosinusitis; nasal polyps; CRSwNP; coagu-lation; FXa; prothrombin fragment 112; thrombin-anti-thrombin complex; tissue factor; FVII; tissue factor pathway inhibitor

资金

  1. National Institutes of Health [KL2 TR001424, K23 AI141694, R01 AI104733, U19 AI106683, P01 145818]
  2. National Natural Science Foundation of China [82171113, 81800888]
  3. Tongji Hospital Outstanding Youth grant [2016YQ04]
  4. Parker B. Francis Fellowship Foundation
  5. American Partnership for Eosinophilic Disorders/American Academy of Allergy, Asthma & Immunology HOPE Pilot Grant Award
  6. Ernest S. Bazley Foundation

向作者/读者索取更多资源

This study investigated the mechanisms and activation pathways of coagulation cascade in chronic rhinosinusitis with nasal polyps (CRSwNP). The results showed increased activation of coagulation cascade, local production of tissue factor (TF) and activated factor VII (FVII) in sinonasal mucosa, and reduced formation of the complex of activated factor X (FXa) and TF pathway inhibitor (TFPI) in nasal polyp tissue. These findings suggest that the extrinsic coagulation pathway may play a role in promoting fibrin deposition in CRSwNP.
Background: Increased activation of the coagulation cascade and diminished fibrinolysis combine to promote fibrin deposition and polyp formation in chronic rhinosinusitis (CRS) with nasal polyps (CRSwNP). More information is needed concerning mechanisms of coagulation in CRSwNP. Objective: We investigated the mechanisms as well as the initiation and regulation of coagulation cascade activation in CRS. Methods: Samples were collected from 135 subjects with CRSwNP, 80 subjects with chronic CRS without nasal polyps (NP), and 65 control subjects. The levels of activated factor X (FXa), prothrombin fragment 1+2 (F1+2), thrombin- antithrombin complex, tissue factor (TF), and TF pathway inhibitor (TFPI) were monitored in CRS by real-time PCR, ELISA, immunohistochemistry, or immunofluorescence. Heteromeric complexes of TF with activated factor VII (FVII) and TF with activated FVII and FXa were assessed by coimmunoprecipitation and Western blotting. Results: Increased levels of FXa, F1+2, and thrombin- antithrombin complex were detected in NP tissue compared to uncinate tissue from CRS and control subjects. Although free TF protein levels were not increased in NP, immunoprecipitation of TF in NP tissue revealed increased complexes of TF with FVII. Local expression of FVII was detected in sinonasal mucosa, and the ratio of TFPI to FXa was lower in NP tissue. Conclusion: The coagulation cascade is associated with NP compared to control and uncinate tissue from CRS patients, and TF and FVII are produced locally in sinonasal mucosa in patients. TF and FVII can activate the extrinsic coagulation pathway, suggesting that this pathway may activate fibrin deposition in CRSwNP. Reduced formation of the complex of FXa and TFPI in NP may reduce natural suppression of the extrinsic coagulation pathway in CRSwNP. (J Allergy Clin Immunol 2022;150:467-76.)

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