دورية أكاديمية

TLR7 Ligation Inhibits TLR8 Responsiveness in IL-27-Primed Human THP-1 Monocytes and Macrophages

التفاصيل البيبلوغرافية
العنوان: TLR7 Ligation Inhibits TLR8 Responsiveness in IL-27-Primed Human THP-1 Monocytes and Macrophages
المؤلفون: Natalya Odoardi, Olena Kourko, Carlene Petes, Sameh Basta, Katrina Gee
المصدر: Journal of Innate Immunity, Pp 1-14 (2021)
بيانات النشر: Karger Publishers, 2021.
سنة النشر: 2021
المجموعة: LCC:Medicine
LCC:Internal medicine
مصطلحات موضوعية: interleukin-27, toll-like receptor 7, toll-like receptor 8, toll-like receptor, interferon, monocytes, macrophages, inflammation, Medicine, Internal medicine, RC31-1245
الوصف: Regulation of proinflammatory cytokine expression is critical in the face of single-stranded RNA (ssRNA) virus infections. Many viruses, including coronavirus and influenza virus, wreak havoc on the control of cytokine expression, leading to the formation of detrimental cytokine storms. Understanding the regulation and interplay between inflammatory cytokines is critical to the identification of targets involved in controlling the induction of cytokine expression. In this study, we focused on how the antiviral cytokine interleukin-27 (IL-27) regulates signal transduction downstream of Toll-like receptor 7 (TLR7) and TLR8 ligation, which recognize endosomal single-stranded RNA. Given that IL-27 alters bacterial-sensing TLR expression on myeloid cells and can inhibit replication of single-stranded RNA viruses, we investigated whether IL-27 affects expression and function of TLR7 and TLR8. Analysis of IL-27-treated THP-1 monocytic cells and THP-1-derived macrophages revealed changes in mRNA and protein expression of TLR7 and TLR8. Although treatment with IL-27 enhanced TLR7 expression, only TLR8-mediated cytokine secretion was amplified. Furthermore, we demonstrated that imiquimod, a TLR7 agonist, inhibited cytokine and chemokine production induced by a TLR8 agonist, TL8-506. Delineating the immunomodulatory role of IL-27 on TLR7 and TLR8 responses provides insight into how myeloid cell TLR-mediated responses are regulated during virus infection.
نوع الوثيقة: article
وصف الملف: electronic resource
اللغة: English
تدمد: 1662-811X
1662-8128
Relation: https://www.karger.com/Article/FullText/515738; https://doaj.org/toc/1662-811X; https://doaj.org/toc/1662-8128
DOI: 10.1159/000515738
URL الوصول: https://doaj.org/article/2e088aacb02248b18bcf860afc08d504
رقم الأكسشن: edsdoj.2e088aacb02248b18bcf860afc08d504
قاعدة البيانات: Directory of Open Access Journals
الوصف
تدمد:1662811X
16628128
DOI:10.1159/000515738