Involvement of Peripheral Monocytes with IL-1β in the Pathogenesis of West Syndrome.
Tomoko TakamatsuGaku YamanakaKoko OhnoKanako HayashiYusuke WatanabeMika TakeshitaShinji SuzukiShinichiro MorichiSoken GoYu IshidaShingo OanaYasuyo KashiwagiHisashi KawashimaPublished in: Journal of clinical medicine (2022)
Neuroinflammation has been implicated in the pathogenesis of West syndrome (WS). Inflammatory cytokines, including interleukin-1β(IL-1β), have been reported to be associated with epilepsy. However, the assessment of cytokine changes in humans is not always simple or deterministic. This study aimed to elucidate the immunological mechanism of WS. We examined the intracellular cytokine profiles of peripheral blood cells collected from 13 patients with WS, using flow cytometry, and measured their serum cytokine levels. These were compared with those of 10 age-matched controls. We found that the WS group had significantly higher percentages of inter IL-1β, interleukin-1 receptor antagonist (IL-1RA)-positive monocytes, and interferon gamma (IFN-γ) in their CD8+ T cells than the control group. Interestingly, the group with sequelae revealed significantly lower levels of intracellular IFN-γ and IL-6 in their CD8+ T and CD4+ T cells, respectively, than the group without sequelae. There was no correlation between the ratios of positive cells and the serum levels of a particular cytokine in the WS patients. These cytokines in the peripheral immune cells might be involved in the neuroinflammation of WS, even in the absence of infectious or immune disease. Overall, an immunological approach using flow cytometry analysis might be useful for immunological studies of epilepsy.
Keyphrases
- flow cytometry
- peripheral blood
- dendritic cells
- induced apoptosis
- cell cycle arrest
- immune response
- end stage renal disease
- lipopolysaccharide induced
- ejection fraction
- peritoneal dialysis
- oxidative stress
- endoplasmic reticulum stress
- inflammatory response
- cognitive impairment
- prognostic factors
- signaling pathway
- systemic lupus erythematosus
- cell death
- cell proliferation
- single cell
- patient reported
- interstitial lung disease
- chemotherapy induced