Multiomic-based immune response profiling in migraine, vestibular migraine and Meniere’s disease
Metadata
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Cruz-Granados, Pablo; Frejo, Lidia; Pérez Carpena, Patricia; Amor Dorado, Juan Carlos; Dominguez Durán, Emilio; Fernandez Nava, Maria Jose; Batuecas Caletrio, Angel; Haro Hernández, Elisheba; Martínez Martínez, Marta; López Escámez, José AntonioEditorial
Wiley Online Library
Materia
Autoinflammation Cytokines Meniere disease
Date
2024-09-18Referencia bibliográfica
Cruz Granados, P. et. al. Immunology. 2024;1–12. [https://doi.org/10.1111/imm.13863]
Sponsorship
K7013-B3414G Grant from University of Sydney; PI20-1126 grant from ISCIII by FEDER Funds from the EU; CLINMON-2 from the Meniere’s Society UK; Postdoctoral Fellowship (CD20/0153)Abstract
Migraine (MI) is the most common neurological disease, affecting with 20% of the
world population. A subset of 25% of MI patients showcase concurrent vestibular
symptoms, which may classify as vestibular migraine (VM). Meniere’s disease
(MD) is a complex inner ear disorder defined by episodes of vertigo associated
with tinnitus and sensorineural hearing loss with a significant autoimmune/
autoinflammatory contribution, which symptoms overlap with VM. Blood samples
from 18 patients with MI (5), VM (5) and MD (8) and 6 controls were collected
and compared in a case–control study. Droplet-isolated nuclei from
mononuclear cells used to generate scRNAseq and scATACseq data sets from MI, VM and MD. MI and VM have no differences in their immune transcriptome;
therefore, they were considered as a single cluster for further analyses. Natural
Killer (NK) cells transcriptomic data support a polarisation triggered by Type
1 innate immune cells via the release of interleukin (IL)-12, IL-15 and IL-18.
According to the monocyte scRNAseq data, there were two MD clusters, one inactive
and one driven by monocytes. The unique pathways of the MI + VM cluster
were cellular responses to metal ions, whereas MD monocyte-driven cluster pathways
showed responses to biotic stimuli. MI and MD have different immune
responses. These findings support that MI and VM have a Type 1 immune lymphoid
cell response, and that there are two clusters of MD patients, one inactive
and one Monocyte-driven.