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A Behavioral Screen for Heat-Induced Seizures in Mouse Models of Epilepsy
Published on: July 12, 2021
Alterations of cell-mediated immune response in children with febrile seizures
T C Montelli1, A M Soares, M R Parise-Fortes
1Department of Neurology and Psychiatry, School of Medicine, State University of São Paulo (UNESP), Botcatu, Brazil.
Insights
Children with febrile seizures often show impaired cellular immunity, with increased CD8+ cells and reduced lymphocyte response. This immune dysfunction may explain frequent infections observed in these patients.
Area of Science:
- Immunology
- Pediatrics
- Neurology
Background:
- Febrile seizures are common in children.
- Recurrent infections are frequently observed in children with febrile seizures.
- The underlying immunological mechanisms are not fully understood.
Purpose of the Study:
- To investigate T-cell subset distribution in children with febrile seizures.
- To assess lymphocyte proliferative response to phytohemagglutinin (PHA).
- To explore potential links between immune status and infection susceptibility.
Main Methods:
- Monoclonal antibody-based T-cell subset analysis in peripheral blood.
- Measurement of lymphocyte proliferation in response to PHA.
- Assessment of plasma inhibitory activity on lymphocyte function.
- Comparison between 30 children with febrile seizures and 14 age-matched controls.
Main Results:
- 64% of patients showed increased CD8+ T-cells.
- A low helper/suppressor T-cell ratio was found in 60% of patients.
- Impaired lymphocyte proliferative response to PHA was observed.
- 33% of patients had plasma with inhibitory activity on lymphocyte function.
Conclusions:
- Children with febrile seizures exhibit impaired cellular immunity.
- Elevated CD8+ cells and reduced lymphocyte responsiveness are key findings.
- Immune dysfunction may contribute to the pathogenesis of febrile seizures and associated infections.
Abstract:
The aim of the present investigation was to study the distribution of T-cell subsets in peripheral blood defined by monoclonal antibodies and by the lymphocyte proliferative response to phytohemagglutinin (PHA) in 30 children with febrile seizures and in 14 age-matched control subjects. Frequent respiratory, urinary and dermatologic infections were observed in 22 patients. The immunologic parameters showed that 64% of the patients presented an increased number of CD8+ cells and a low helper/suppressor ratio was observed in 60% of the patients. In addition, the proliferative response of lymphocytes to PHA was impaired in the patients. It was observed the presence of inhibitory activity on lymphocyte function in the plasma of 33% of children with febrile seizures. These results suggest that patients with febrile seizures have an impairment of cellular immunity that may be connected with this epileptic syndrome and explain the infections observed.
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