Combined Treatment With H1 and H4 Receptor Antagonists Improves Th2 Inflammatory Responses in the Nasal Mucosa of Allergic Rhinitis Rats

• Published in: American journal of rhinology & allergy 2021-11, Vol.35 (6), p.809-816
• Main Authors: Wang, Weiwei, Yu, Hongwei, Pan, Yongliang, Shao, Shengwen
• Format: Article
• Language: English
• Subjects: Animals; Disease Models, Animal; Histamine Antagonists - therapeutic use; Nasal Mucosa - immunology; Rats; Rats, Sprague-Dawley; Receptors, Histamine H3; Receptors, Histamine H4 - antagonists & inhibitors; Rhinitis, Allergic - drug therapy; Rhinitis, Allergic - immunology; Th2 Cells - immunology
• ISSN: 1945-8924; 1945-8932
• DOI: 10.1177/19458924211002604

Background Histamine H1 receptor (H1R) antagonists are the first-line drugs for the treatment of allergic rhinitis (AR) at present. Emerging evidence supports an important role of histamine H4 receptor (H4R) in allergic diseases. However, information regarding the effects of combined treatment with H1 and H4 receptor antagonists in AR is limited. Objectives We aimed to assess the effects of combined treatment with H1R and H4R antagonists on Th2 inflammatory responses in the nasal mucosa of AR rats. Methods Sprague Dawley rats were sensitized with ovalbumin and treated with H1R antagonist desloratadine or/and H4R antagonist JNJ7777120. Western blotting was used to assay the phenotypic markers of mature dendritic cells in the nasal mucosa, including major histocompatibility complex class II (MHC-II) and co-stimulatory molecules CD80, CD86 and OX40 ligand (OX40L). Th2 inflammatory cytokines including interleukin-4, 5 and 13 in nasal lavage fluids were determined by using enzyme-linked immunoassay. Results The treatment with desloratadine alone down-regulated the CD86 expression, and decreased the production of Th2 cytokines, but had no impact on the expression of MHC-II, CD80 and OX40L. The administration of NJ7777120 alone reduced the levels of CD86, OX40L and Th2 cytokines, whereas MHC-II and CD80 expression was unaffected. The combination of desloratadine and JNJ7777120 showed more significant synergistic therapeutic effects than monotherapy. Conclusion H4R antagonist acted synergistically with H1R antagonist to reduce Th2 inflammatory responses by down-regulating CD86 and OX40L expression in the nasal mucosa of AR rats. The combination with H1R and H4R antagonists might be a new strategy for AR treatment.