TY - JOUR
T1 - Significance of IgG4-positive cells in severe eosinophilic chronic rhinosinusitis
AU - Koyama, Takahisa
AU - Kariya, Shin
AU - Sato, Yasuharu
AU - Gion, Yuka
AU - Higaki, Takaya
AU - Haruna, Takenori
AU - Fujiwara, Tazuko
AU - Minoura, Akira
AU - Takao, Soshi
AU - Orita, Yorihisa
AU - Kanai, Kengo
AU - Taniguchi, Masami
AU - Nishizaki, Kazunori
AU - Okano, Mitsuhiro
N1 - Funding Information:
The authors would like to thank Yuko Okano for their editorial assistance. This work was supported in part by grants from Ministry of Education, Culture, Sports, Science and Technology , Japan ( 16K15721 and 17K16920 ); a grant for Intractable Diseases (IgG4-related disease research program) from the Ministry of Health, Labour and Welfare , Japan; and grants from the Japan Agency for Medical Research and Development under Grant Number JP17ek0410040 , and JP16ek0109062 .
Publisher Copyright:
© 2018 Japanese Society of Allergology
PY - 2019/4
Y1 - 2019/4
N2 - Background: IgG4 production is regulated by type 2 (IL-4 and IL-13) and regulatory (IL-10) cytokines involved in the pathophysiology of chronic rhinosinusitis (CRS). We sought to determine the pathophysiological characteristics of IgG4-positive cells in sinonasal tissues in CRS, especially eosinophilic CRS (ECRS). Methods: IgG4-positive cells in uncinate tissues (UT) and nasal polyps (NP) were examined by immunohistochemistry. Associations between the number of IgG4-positive cells and clinicopathological factors were analyzed. Receiver operating characteristics (ROC) analysis was performed to determine the cut-off value of IgG4-positive cells in tissue that can predict the post-operative course. Results: IgG4 was mainly expressed in infiltrating plasma and plasmacytoid cells, and the number of IgG4-positive cells was significantly higher in NP, especially those from severe ECRS patients, than in UT. In CRS patients, the number of IgG4-positive cells significantly and positively correlated with blood and tissue eosinophilia, radiological severity, and serum level of total IgE. The number of infiltrating IgG4-positive cells was significantly higher in patients with a poor post-operative course (sustained sinus shadow 6 months after surgery) than in those with a good one. The number of IgG4-positive cells in NP could discriminate patients with a good or a poor post-operative course (area under the curve: 0.769). Also, 73.3% sensitivity and 82.5% specificity were achieved when the cut-off value was set at 17 cells/high-power field. Conclusions: Our results suggest that the local expression of IgG4 on cells may be used as a biomarker that reflects the pathophysiology of CRS, including the post-operative course.
AB - Background: IgG4 production is regulated by type 2 (IL-4 and IL-13) and regulatory (IL-10) cytokines involved in the pathophysiology of chronic rhinosinusitis (CRS). We sought to determine the pathophysiological characteristics of IgG4-positive cells in sinonasal tissues in CRS, especially eosinophilic CRS (ECRS). Methods: IgG4-positive cells in uncinate tissues (UT) and nasal polyps (NP) were examined by immunohistochemistry. Associations between the number of IgG4-positive cells and clinicopathological factors were analyzed. Receiver operating characteristics (ROC) analysis was performed to determine the cut-off value of IgG4-positive cells in tissue that can predict the post-operative course. Results: IgG4 was mainly expressed in infiltrating plasma and plasmacytoid cells, and the number of IgG4-positive cells was significantly higher in NP, especially those from severe ECRS patients, than in UT. In CRS patients, the number of IgG4-positive cells significantly and positively correlated with blood and tissue eosinophilia, radiological severity, and serum level of total IgE. The number of infiltrating IgG4-positive cells was significantly higher in patients with a poor post-operative course (sustained sinus shadow 6 months after surgery) than in those with a good one. The number of IgG4-positive cells in NP could discriminate patients with a good or a poor post-operative course (area under the curve: 0.769). Also, 73.3% sensitivity and 82.5% specificity were achieved when the cut-off value was set at 17 cells/high-power field. Conclusions: Our results suggest that the local expression of IgG4 on cells may be used as a biomarker that reflects the pathophysiology of CRS, including the post-operative course.
KW - Chronic rhinosinusitis
KW - Eosinophils
KW - IgG4
KW - Nasal polyps
KW - Severity
UR - http://www.scopus.com/inward/record.url?scp=85054457826&partnerID=8YFLogxK
UR - http://www.scopus.com/inward/citedby.url?scp=85054457826&partnerID=8YFLogxK
U2 - 10.1016/j.alit.2018.09.002
DO - 10.1016/j.alit.2018.09.002
M3 - Article
C2 - 30316748
AN - SCOPUS:85054457826
SN - 1323-8930
VL - 68
SP - 216
EP - 224
JO - Allergology International
JF - Allergology International
IS - 2
ER -