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Inverse correlation of soluble programmed cell death-1 ligand-1 (sPD-L1) with eosinophil count and clinical severity in allergic rhinitis patients.

Authors :
Nasiri Kalmarzi, Rasoul
Fattahi, Nima
Kaviani, Zeinab
Ataee, Pedram
Mansouri, Majid
Moradi, Ghobad
Yousefzade, Alireza
Abbassi, Javid Morad
Source :
Allergology International. Apr2017, Vol. 66 Issue 2, p326-331. 6p.
Publication Year :
2017

Abstract

Background T-cell response outcome is determined by co-stimulatory/inhibitory signals. Programmed cell death-1 ligand-1 (PD-L1) is a member of these co-signaling molecules with known soluble form in human serum. Soluble PD-L1 (sPD-L1) is also recognized in patients with some types of malignancy or autoimmune disorders, though there are few studies on sPD-L1 roles in allergic diseases. The purpose of this survey was to evaluate the association between sPD-L1 levels with eosinophil count as well as disease severity in allergic rhinitis (AR) patients. Methods 90 patients with AR were selected. Disease severity was determined by a modified Allergic Rhinitis and its Impact on Asthma (ARIA) classification as mild, moderate and severe. Whole blood samples were collected. Then eosinophil count and serum sPD-L1 were detected by a hematologic analyzer and a commercial ELISA kit. Results 13 (14.44%), 31 (34.44%), and 46 (51.12%) of patients had mild, moderate and severe disease, respectively. The mean levels of sPD-L1 and eosinophil count were ascertained 18.38 ± 14.42 ng/ml and 422.43 ± 262.26 cell/μl. A significant inverse correlation was determined between sPD-L1 levels and eosinophil count (r = −0.364, P < 0.001). Moreover, we detected a significant negative association between sPD-L1 levels and disease severity (r = −0.384, P < 0.001). Conclusions It is deduced that sPD-L1 can be used as a helpful marker to determine the severity of AR. Furthermore, this study indicated that sPD-L1 may have an inhibitory role in AR development, and its modulation may be considered as a useful accessory therapeutic approach for reduction of AR progression. [ABSTRACT FROM AUTHOR]

Details

Language :
English
ISSN :
13238930
Volume :
66
Issue :
2
Database :
Academic Search Index
Journal :
Allergology International
Publication Type :
Academic Journal
Accession number :
122118897
Full Text :
https://doi.org/10.1016/j.alit.2016.08.008