Case-Control Study: Evaluating the Role and Therapeutic Potential of FSTL1 in Type 2 Inflammation of Chronic

Bingjie Huang1,2, Jingyun Zhu1, Xiangbin Chai3

  • 1First Clinical Medical College, Shanxi Medical University, Taiyuan, 030000, People's Republic of China.

PubMed
Abstract

Insights

Follicle suppressor-like protein 1 (FSTL1) is elevated in chronic sinusitis, particularly in eosinophilic CRS (ECRS). FSTL1 correlates with type 2 inflammation markers, suggesting it may be a therapeutic target for ECRS.

Area of Science:

  • Immunology
  • Otorhinolaryngology
  • Molecular Biology

Background:

  • Follicle suppressor-like protein 1 (FSTL1) is implicated in chronic inflammatory conditions like asthma and COPD.
  • The role of FSTL1 in chronic sinusitis with nasal polyps (CRSwNP) has not been extensively studied.
  • Type 2 inflammation is a key feature in CRSwNP pathogenesis.

Purpose of the Study:

  • To investigate the expression levels of FSTL1 in patients with chronic sinusitis.
  • To explore the potential association between FSTL1 expression and type 2 inflammation in chronic sinusitis, specifically CRSwNP.

Main Methods:

  • Study included 34 CRSwNP patients (24 ECRS, 10 non-ECRS) and 10 controls.
  • Pathomorphological changes were assessed using Hematoxylin-Eosin (HE) staining.
  • Expression of FSTL1 and type 2 cytokines (IL-4, IL-5, IL-13) was evaluated using Immunohistochemistry (IHC), qRT-PCR, and Western Blotting (WB).

Main Results:

  • ECRS tissues showed thickened mucosa, gland hyperplasia, and significant inflammatory cell and eosinophil infiltration.
  • FSTL1 and type 2 inflammatory cytokines (IL-4, IL-5, IL-13) were significantly upregulated in both ECRS and non-ECRS groups compared to controls (P<0.05).
  • A positive correlation was observed between FSTL1 and IL-4, IL-5, and IL-13 levels in the ECRS group (P<0.05).

Conclusions:

  • FSTL1 is highly expressed in chronic sinusitis tissues.
  • FSTL1 expression is positively correlated with key type 2 inflammatory markers in ECRS.
  • FSTL1 may contribute to the pathogenesis of type 2 inflammation in ECRS and could represent a potential therapeutic target.

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