Altered ocular surface immune cell profile in patients with dry eye disease

免疫系统 CD8型 免疫学 流式细胞术 医学 T细胞 细胞 生物 遗传学
作者
Archana Padmanabhan Nair,Sharon D’Souza,Rohit Shetty,Prerna Ahuja,Gairik Kundu,Pooja Khamar,Zelda Dadachanji,Prajakta Paritekar,Pavitra Patel,Mor M. Dickman,Rudy M.M.A. Nuijts,Rajiv R. Mohan,Arkasubhra Ghosh,Swaminathan Sethu
出处
期刊:Ocular Surface [Elsevier BV]
卷期号:21: 96-106 被引量:37
标识
DOI:10.1016/j.jtos.2021.04.002
摘要

Abstract Purpose Aberrant inflammation and immune dysregulation are known pathogenic contributors in dry eye disease (DED). Aim of the study was to determine the proportions of immune cell subsets on the ocular surface (OS) of DED patients. Methods 15 healthy controls (22 eyes) and 48 DED subjects (36 eyes with evaporative DED – EDED; 60 eyes with aqueous deficient DED – ADED) were included in the study. Tear break up time (TBUT), Schirmer's test 1 (ST1), corneal staining (CS) and ocular surface disease index (OSDI) scoring were recorded. OS wash was used to collect immune cells on the OS of study subjects. The cells immunophenotyped using flow cytometry include leukocytes, neutrophils, macrophages, natural killer–NK cells and T cell subsets (CD4; CD8; double positive–DP; gamma delta–γδ and NK T cells). Results Significantly higher proportions of leukocytes, neutrophils, CD4 T cells, CD8 T cells, DP T cells and CD4/CD8 T cells ratio were observed in EDED and/or ADED patients. Significantly higher proportions of neutrophils and lower proportions of NK cells were observed in ADED subjects with corneal staining compared to those without and controls. Neutrophils/NK cells ratio was significantly higher in EDED and ADED subjects compared to controls. Correlation analysis revealed pathological relationships between proportions of leukocytes, neutrophils, CD4 T cells and Neutrophil/NK cells ratio with DED clinical parameters. Conclusion OS immune cell subset proportion changes in DED patients were associated with DED types and severity. The data suggests the potential for a new generation of therapies targeting immune cells on the ocular surface.
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