PMID- 35153491 OWN - NLM STAT- PubMed-not-MEDLINE LR - 20220501 IS - 1178-6965 (Print) IS - 1178-6965 (Electronic) IS - 1178-6965 (Linking) VI - 15 DP - 2022 TI - Role of Thymus and Activation-Regulated Chemokine in Allergic Asthma. PG - 157-167 LID - 10.2147/JAA.S351720 [doi] AB - BACKGROUND: Asthma is a chronic inflammatory airway disease characterized by the predominant infiltration of inflammatory cells in the airways. Thymus and activation-regulated chemokine/C-C motif chemokine 17 (TARC/CCL17) is a chemokine responsible for trafficking T helper 2 cells into sites of allergic inflammation. OBJECTIVE: To validate the role of TARC in association with clinical and inflammatory parameters in adult asthmatics. METHODS: We enrolled 128 asthmatic patients and 70 healthy controls (HCs). Asthma-related clinical and laboratory parameters, including lung function and eosinophil counts, were measured. Serum levels of TARC, free immunoglobulin E (IgE), and eosinophil-derived neurotoxin (EDN) were determined by using enzyme-linked immunosorbent assay; serum total IgE level was measured using ImmunoCAP. The levels of inflammatory lipid mediators, such as leukotriene E4 (LTE4), 15-hydroxyeicosatetraenoic acid (15-HETE), thromboxane B2 (TXB2), and prostaglandin F2alpha (PGF2alpha), were measured by liquid chromatography-tandem mass spectrometry. RESULTS: Serum TARC levels are significantly higher in asthmatics than in HCs and in allergic asthmatics than in HCs (P < 0.010 for all), with significantly negative correlations between serum TARC levels and FEV(1)%/MMEF% values (r = -0.314, r = -0.268, P < 0.050 for both). The patients with higher serum TARC levels had higher levels of serum total and free IgE levels (P < 0.050 for both) with positive correlations to serum levels of EDN, TXB2, and 15-HETE (r = 0.233, r = 0.264, and r = 0.223, respectively, P < 0.050 for all). CONCLUSION: We suggest the role of TARC in allergic asthma via contributing to mast cell and eosinophilic inflammation. CI - (c) 2022 Luu Quoc et al. FAU - Luu Quoc, Quang AU - Luu Quoc Q AUID- ORCID: 0000-0003-2183-8171 AD - Department of Allergy and Clinical Immunology, Ajou University School of Medicine, Suwon, South Korea. FAU - Moon, Ji-Young AU - Moon JY AD - Department of Allergy and Clinical Immunology, Ajou University School of Medicine, Suwon, South Korea. FAU - Lee, Dong-Hyun AU - Lee DH AD - Department of Allergy and Clinical Immunology, Ajou University School of Medicine, Suwon, South Korea. FAU - Ban, Ga-Young AU - Ban GY AUID- ORCID: 0000-0002-7961-742X AD - Department of Pulmonary, Allergy, and Critical Care Medicine, Kangdong Sacred Heart Hospital, Hallym University College of Medicine Institute for Life Sciences, Chuncheon, South Korea. FAU - Kim, Seung-Hyun AU - Kim SH AD - Translational Research Laboratory for Inflammatory Disease, Clinical Trial Center, Ajou University Medical Center, Suwon, South Korea. FAU - Park, Hae-Sim AU - Park HS AUID- ORCID: 0000-0003-2614-0303 AD - Department of Allergy and Clinical Immunology, Ajou University School of Medicine, Suwon, South Korea. LA - eng PT - Journal Article DEP - 20220205 PL - New Zealand TA - J Asthma Allergy JT - Journal of asthma and allergy JID - 101543450 PMC - PMC8828566 OTO - NOTNLM OT - IgE OT - T cells OT - allergic asthma OT - asthma OT - eosinophils OT - mast cells OT - thymus and activation-regulated chemokine COIS- The authors report no conflicts of interest for this work and that there are no financial or other issues that might lead to conflicts of interest. EDAT- 2022/02/15 06:00 MHDA- 2022/02/15 06:01 PMCR- 2022/02/05 CRDT- 2022/02/14 05:28 PHST- 2021/11/30 00:00 [received] PHST- 2022/01/22 00:00 [accepted] PHST- 2022/02/14 05:28 [entrez] PHST- 2022/02/15 06:00 [pubmed] PHST- 2022/02/15 06:01 [medline] PHST- 2022/02/05 00:00 [pmc-release] AID - 351720 [pii] AID - 10.2147/JAA.S351720 [doi] PST - epublish SO - J Asthma Allergy. 2022 Feb 5;15:157-167. doi: 10.2147/JAA.S351720. eCollection 2022.