Single-cell immune profiling of Meniere Disease patients

被引:11
|
作者
Flook, Marisa [1 ,2 ,3 ]
Escalera-Balsera, Alba [1 ,2 ,3 ]
Rybakowska, Paulina [4 ]
Frejo, Lidia [1 ,2 ,3 ]
Batuecas-Caletrio, Angel [5 ,6 ]
Amor-Dorado, Juan C. [7 ]
Soto-Varela, Andres [8 ,9 ]
Alarcon-Riquelme, Marta [4 ]
Lopez-Escamez, Jose A. [1 ,2 ,3 ,10 ,11 ]
机构
[1] Ctr Genom & Oncol Res Pfizer Univ Granada Andalusi, Otol & Neurotol Grp CTS 495, Dept Genom Med, GENYO,PTS Granada, Granada, Spain
[2] Univ Granada, Div Otolaryngol, Dept Surg, Inst Invest Biosanitaria,Ibs GRANADA, Granada, Spain
[3] Ctr Invest Biomed Red Enfermedades Raras CIBERER, Sensorineural Pathol Programme, Madrid, Spain
[4] Ctr Genom & Oncol Res Pfizer Univ Granada Andalusi, Genet Complex Dis Grp, Dept Genom Med, GENYO, Granada, Spain
[5] Hosp Univ Salamanca, Dept Otolaryngol, Inst Invest Biome Salamanca IBSAL, Salamanca, Spain
[6] Univ Salamanca, Dept Surg, Div Otolaryngol, Salamanca, Spain
[7] Hosp Can Misses, Dept Otolaryngol, Ibiza, Spain
[8] Complexo Hosp Univ, Dept Otorhinolaryngol, Div Otoneurol, Santiago De Compostela, Spain
[9] Univ Santiago De Compostela, Dept Surg & Med Surg Special, Santiago De Compostela, Spain
[10] Univ Sydney, Kolling Inst, Fac Med & Hlth, Sch Med Sci,Menieres Dis Neurosci Res Program, Sydney, NSW, Australia
[11] PTS Granada, Otol & Neurotol Grp CTS495, GENYO, Ave Ilustrac 114, Granada 18016, Spain
基金
欧盟地平线“2020”;
关键词
Allergy; Inflammation; Cytokines; Mass cytometry; Meniere Disease; HEARING-LOSS; PROTEIN-1; ALLERGY; TNF; CSF;
D O I
10.1016/j.clim.2023.109632
中图分类号
R392 [医学免疫学]; Q939.91 [免疫学];
学科分类号
100102 ;
摘要
Background: Meniere Disease (MD) is an inner ear syndrome, characterized by episodes of vertigo, tinnitus and fluctuating sensorineural hearing loss. The pathological mechanism leading to sporadic MD is still poorly understood, however an allergic inflammatory response seems to be involved in some patients with MD. Objective: Decipher an immune signature associated with the syndrome. Methods: We performed mass cytometry immune profiling on peripheral blood from MD patients and controls. We analyzed differences in state and differences in abundance of the different cellular subsets. IgE levels were quantified through ELISA on supernatant of cultured whole blood. Results: We have identified two clusters of individuals according to the single cell cytokine profile. These clusters presented differences in IgE levels, immune cell population abundance, including a reduction of CD56dim NKcells, and changes in cytokine expression with a different response to bacterial and fungal antigens. Conclusion: Our results support a systemic inflammatory response in some MD patients that show a type 2 response with allergic phenotype, which could benefit from personalized IL-4 blockers.
引用
收藏
页数:10
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