TY - JOUR
T1 - Alleviating effect of intranasal zinc on symptoms of allergic rhinitis
AU - Xu, Huadong
AU - Tong, Keming
AU - Iwasaki, Naruhito
AU - Ohgami, Nobutaka
AU - Tazaki, Akira
AU - Kagawa, Takumi
AU - Gao, Yanjun
AU - Nishadhi, Delgama A.S.M.
AU - Harusato, Akihito
AU - Sakashita, Masafumi
AU - Ogi, Kazuhiro
AU - Fujieda, Shigeharu
AU - Sumiya, Shogo
AU - Iwasaki, Shinichi
AU - Kato, Masashi
N1 - Publisher Copyright:
© 2025 The Author(s)
PY - 2025/5
Y1 - 2025/5
N2 - Background: There is no information about the clinical implications and kinetics of zinc (Zn) in the nasal cavity, a center of allergic inflammation, and serum in subjects with allergic rhinitis (AR). Objective: Effects of intranasal Zn on symptoms before and after allergen provocation were investigated in humans and mice with or without AR. Methods: The first clinical follow-up study for Zn levels in nasal epithelial lining fluid (ELF) and serum was conducted in 57 control subjects and 44 patients with Japanese cedar pollinosis (JCP), a representative seasonal AR, from preseason to season. The clinical implications and kinetics of Zn levels in ELF and serum were further investigated in model mice with JCP. Results: This clinical study showed that the Zn level in nasal ELF from patients with JCP was increased after pollen exposure and became significantly higher than that in nasal ELF from controls in the JCP season. Conversely, the serum Zn level in patients was decreased after pollen exposure and became significantly lower than that in the controls in the JCP season. To further investigate the clinical implication of Zn level, model mice that mimicked the kinetics of intranasal and serum Zn levels as well as the symptoms in patients with JCP were established. The mouse interventional study showed that the symptoms of mice with provocative JCP were significantly improved by treatment with the putative human-equivalent dose of Zn. The relative number of mucin-secreting goblet cells, a sign of provocative allergic rhinitis, in the mice was decreased by intranasal treatment with Zn. Conclusion: The study's behavioral and pathologic results indicate that an increased level of intranasal Zn can alleviate symptoms of AR.
AB - Background: There is no information about the clinical implications and kinetics of zinc (Zn) in the nasal cavity, a center of allergic inflammation, and serum in subjects with allergic rhinitis (AR). Objective: Effects of intranasal Zn on symptoms before and after allergen provocation were investigated in humans and mice with or without AR. Methods: The first clinical follow-up study for Zn levels in nasal epithelial lining fluid (ELF) and serum was conducted in 57 control subjects and 44 patients with Japanese cedar pollinosis (JCP), a representative seasonal AR, from preseason to season. The clinical implications and kinetics of Zn levels in ELF and serum were further investigated in model mice with JCP. Results: This clinical study showed that the Zn level in nasal ELF from patients with JCP was increased after pollen exposure and became significantly higher than that in nasal ELF from controls in the JCP season. Conversely, the serum Zn level in patients was decreased after pollen exposure and became significantly lower than that in the controls in the JCP season. To further investigate the clinical implication of Zn level, model mice that mimicked the kinetics of intranasal and serum Zn levels as well as the symptoms in patients with JCP were established. The mouse interventional study showed that the symptoms of mice with provocative JCP were significantly improved by treatment with the putative human-equivalent dose of Zn. The relative number of mucin-secreting goblet cells, a sign of provocative allergic rhinitis, in the mice was decreased by intranasal treatment with Zn. Conclusion: The study's behavioral and pathologic results indicate that an increased level of intranasal Zn can alleviate symptoms of AR.
KW - Allergic rhinitis
KW - Japanese cedar pollinosis
KW - intranasal exposure
KW - nasal epithelial lining fluid
KW - zinc
UR - http://www.scopus.com/inward/record.url?scp=85216500724&partnerID=8YFLogxK
UR - http://www.scopus.com/inward/citedby.url?scp=85216500724&partnerID=8YFLogxK
U2 - 10.1016/j.jacig.2025.100408
DO - 10.1016/j.jacig.2025.100408
M3 - Article
AN - SCOPUS:85216500724
SN - 2772-8293
VL - 4
JO - Journal of Allergy and Clinical Immunology: Global
JF - Journal of Allergy and Clinical Immunology: Global
IS - 2
M1 - 100408
ER -