Two-Track Medical Treatment Strategy According to the Clinical Scoring System for Chronic Rhinosinusitis

• Published in: Allergy, asthma & immunology research 2018, Asthma & Immunology Research, 10(5), , pp.490-502
• Main Authors: Kim, Dong Kyu, Kang, Seong Il, Kong, Il Gyu, Cho, Young Hoon, Song, Seul Ki, Hyun, Se Jin, Cho, Sung Dong, Han, Sang Yoon, Cho, Seong Ho, Kim, Dae Woo
• Format: Article
• Language: English
• Subjects: Chemokines; Classification; Collagen (type I); Cytokines; Data processing; Foxp3 protein; GATA-3 protein; Gene expression; Health services; Immunoassay; Immunology; Inflammation; Interleukin 10; Interleukin 13; Interleukin 22; Interleukin 5; Leukocytes (eosinophilic); Medical treatment; Original; Patients; Principal components analysis; Proteins; Rhinosinusitis; Subgroups; Thymic stromal lymphopoietin; Thymus; Transcription factors; γ-Interferon; 내과학
• ISSN: 2092-7355; 2092-7363
• DOI: 10.4168/aair.2018.10.5.490

The previously reported Japanese clinical scoring study (JESREC) suggests that chronic rhinosinusitis (CRS) can be divided into 4 subtypes according to the degree of eosinophilic CRS (ECRS) and offers the information regarding the prognosis of CRS to clinicians. However, this scoring system has not yet been validated by an immunological study and needs to provide treatment guidelines based on underlying immunologic profiles. We investigated the immunologic profile of each CRS subgroup according to the JESREC classification and suggest its clinical application. A total of 140 CRS patients and 20 control subjects were enrolled. All patients were classified into 4 groups according to the JESREC (non-, mild, moderate and severe ECRS). Nasal tissues were analyzed for mRNA expression of major cytokines (IL-5, IL-10, IL-13, IL-17A, IL-22, IL-23p19, IFN-γ, periostin, thymic stromal lymphopoietin [TSLP] and ST2), major chemokines (CCL11, CCL24, CXCL1 and CXCL2), transcription factors (T-bet, GATA3, RORC and FOXP3) and COL1A1 for type I collagen. Protein levels of 3 major cytokines (IL-5, IL-17A and IFN-γ) were also measured by multiplex immunoassay. Principal component analysis (PCA) was conducted to investigate the overall profile of multiple mediators. The moderate/severe ECRS showed up-regulation of type 2-related mediators (IL-5, IL-13, periostin, TSLP and ST-2), whereas INF-γ (type 1 cytokine) and CXCL1 (neutrophil chemokine) expressions were increased in non-/mild ECRS compared with moderate/severe ECRS. The JESREC classification reflected an immunological endotype. In PCA data, PCA1 indicates a relative type 2 profile, whereas PCA2 represents a type 1/type 17-related profile. In this analysis, mild ECRS was indistinguishable from non-ECRS, whereas moderate to severe ECRS showed a distinct distribution compared with non-ECRS. The JESREC classification could be divided into 2 categories, non-/mild vs. moderate/severe ECRS based on underlying immunological analyses. The CRS clinical scoring system from the JESREC study reflects an inflammatory endotype. However, the immunologic profile of mild ECRS was similar to that of non-ECRS. Therefore, we propose type 2-targeted medical treatment for moderate to severe ECRS and type 1/type 17-targeted for non-ECRS and mild ECRS as the first treatment option.