PMID- 30716814 OWN - NLM STAT- PubMed-not-MEDLINE LR - 20191120 IS - 2096-7993 (Print) IS - 2096-7993 (Linking) VI - 32 IP - 22 DP - 2018 Nov TI - [Treg influences the pathogenesis of allergic rhinitis through TICAM-1 pathway]. PG - 1763-1766 LID - 10.13201/j.issn.1001-1781.2018.22.020 [doi] AB - Allergic rhinitis is an immunoglobulin E (IgE)-mediated type I allergic disorder of the nasal mucosa, which is caused by an imbalance in the cytokine network, a number of intracellular signaling pathways being actived. Treg is known to have immunosuppressive effects. Numerous studies have shown that Toll-like receptors play an important immunomodulatory role in the pathogenesis of allergic rhinitis, and TICAM-1, as an important adaptor protein in the Toll-like receptor domain, is involved in signal transduction of allergic rhinitis. This article reviews Treg's impact on the pathogenesis of allergic rhinitis through the TICAM-1 pathway to further understand the role of allergic rhinitis in the pathogenesis and to provide new ideas for therapeutic goals for allergic rhinitis. CI - Copyright(c) by the Editorial Department of Journal of Clinical Otorhinolaryngology Head and Neck Surgery. FAU - Zhang, L X AU - Zhang LX FAU - Liu, T AU - Liu T LA - chi PT - English Abstract PT - Journal Article PT - Review PL - China TA - Lin Chuang Er Bi Yan Hou Tou Jing Wai Ke Za Zhi JT - Lin chuang er bi yan hou tou jing wai ke za zhi = Journal of clinical otorhinolaryngology, head, and neck surgery JID - 101303164 OTO - NOTNLM OT - rhinitis, allergic OT - TICAM-1 OT - Treg COIS- The authors of this article and the planning committee members and staff have no relevant financial relationships with commercial interests to disclose. EDAT- 2019/02/06 06:00 MHDA- 2019/02/06 06:01 CRDT- 2019/02/06 06:00 PHST- 2018/06/05 00:00 [received] PHST- 2019/02/06 06:00 [entrez] PHST- 2019/02/06 06:00 [pubmed] PHST- 2019/02/06 06:01 [medline] AID - 10.13201/j.issn.1001-1781.2018.22.020 [doi] PST - ppublish SO - Lin Chuang Er Bi Yan Hou Tou Jing Wai Ke Za Zhi. 2018 Nov;32(22):1763-1766. doi: 10.13201/j.issn.1001-1781.2018.22.020.