FABP5 as a possible biomarker in atopic march: FABP5-induced Th17 polarization, both in mouse model and human samples
Autor: | Ji Hye Kim, Jung Won Park, Thomas S. Kupper, Jungsoo Lee, Ke Lun Zhang, Youdong Pan, Kyung Hee Park, Seo Hyeong Kim, Jongsun Lee, Ji Yeon Noh, HyeRan Kim, Chang Ook Park, Bomi Kim, Kyoung Yong Jeong, Kwang Hoon Lee, Howard Chu, Zheng-wang Sun |
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Jazyk: | angličtina |
Rok vydání: | 2020 |
Předmět: |
0301 basic medicine
CD4-Positive T-Lymphocytes Male Research paper AHR Airway hyperresponsiveness medicine.medical_treatment Th1 Type 1 helper T cells lcsh:Medicine AA Allergic asthma medicine.disease_cause AR Allergic rhinitis Mice 0302 clinical medicine Allergen EASI Eczema area and severity index IL-17A TRC The RNAi Consortium D. farinae Dermatophagoides farinae TSLP Thymic stromal lymphopoietin Sensitization Cells Cultured Oligonucleotide Array Sequence Analysis lcsh:R5-920 medicine.diagnostic_test Cell Polarity Fatty-acid-binding protein 5 General Medicine Atopic dermatitis Middle Aged Up-Regulation Real-time polymerase chain reaction Cytokine medicine.anatomical_structure ELISA Enzyme-linked immunosorbent assay 030220 oncology & carcinogenesis Disease Progression AD Atopic dermatitis Biomarker (medicine) Female TRM Tissue-resident memory T Th17 lcsh:Medicine (General) HC Healthy controls Atopic march Adult Genetic Markers Thymic stromal lymphopoietin Fatty Acid-Binding Proteins General Biochemistry Genetics and Molecular Biology Flow cytometry Dermatitis Atopic shRNA Short-hairpin ribonucleic acid 03 medical and health sciences Young Adult AM Atopic march medicine Animals Humans Antigens Dermatophagoides HDM House dust mite FABP Fatty acid-binding protein E-FABP Epidermal fatty acid-binding protein KO knockout business.industry Th2 Type 2 helper T cells lcsh:R Dendritic Cells SDS Sodium dodecyl sulfate medicine.disease ROR Retinoic acid-related orphan receptor Coculture Techniques Disease Models Animal FABP5L Fatty acid-binding protein5-like 030104 developmental biology Case-Control Studies Immunology Th17 Type 17 helper T cells Th17 Cells Der f 1 Dermatophagoides farinae 1 business qRT-PCR Quantitative real-time polymerase chain reaction |
Zdroj: | EBioMedicine, Vol 58, Iss, Pp 102879-(2020) EBioMedicine |
ISSN: | 2352-3964 |
Popis: | Background While the incidence of patients with atopic dermatitis (AD) with atopic march (AM) showing respiratory allergy is steadily rising, the pathomechanism is still unknown. There are currently no biomarkers to predict progression of AM. Methods To explore the mechanism of AM, patients with AD and AM and healthy controls were recruited and RNA microarray, flow cytometry, quantitative real-time polymerase chain reaction, and immunofluorescence staining were performed. We also co-cultured dendritic cells and CD4+ T cells with various Dermatophagoides farinae allergen fractions. Cytokine levels were evaluated using enzyme-linked immunosorbent assay. Findings Both fatty-acid-binding protein 5 (FABP5) and Th17-related genes were more highly expressed in AM. FABP5 knockdown significantly decreased Th17-inducing cytokines in keratinocytes and IL-17A in T cells from AM patients. Further confirmation was obtained using an AM mice model compared to mice without AM. Der f 1, a major D. farinae allergen, increased FABP5 and IL-17A expression in T cells from AM patients. Higher serum FABP5 levels from AM patients were positively correlated with serum IL-17A levels. Interpretation FABP5 expression, possibly enhanced by higher epicutaneous and respiratory sensitization to Der f 1, may directly promote Th17 responses in AD patients with AM. Thus, AM progression can be explained by Th17 reaction induced by FABP5. FABP5 was identified as a potential biomarker in AM. Funding This study was supported by the National Research Foundation of Korea (NRF) grant funded by the Korea government (Ministry of Science and ICT; No. NRF-2017R1A2B4009568), grants of the Korean Health Technology R&D Project, Ministry for Health, Welfare & Family Affairs, and the Republic of Korea (HI13C0010, HI14C1324, HI14C1799). |
Databáze: | OpenAIRE |
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