粘膜免疫学研究ジャーナル

抽象的な

Does Sepsis-Associated Encephalopathy Begin and End with T Cells?

Masafumi Saito

A recent study revealed that 20%-40% of sepsis survivors suffer from mental disorders, more than a year after being discharged from the hospital. Although sepsis-associated encephalopathy (SAE) is complicated by septic conditions and is critically associated with increased mortality, it also leads to neurological dysfunction, which includes mental impairments. Therefore, finding a suitable treatment for neurological dysfunction is of vital importance for the survival and long-term prognosis of patients who contracted sepsis. Neuro-inflammation is the major pathogenesis of SAE, which is caused by the infiltration of inflammatory monocytes into the brain and by the activation of glial cells. However, the mechanism by which T cells are involved in the pathogenesis of SAE remains unclear. This review attempts to understand the underlying mechanisms associated with glial cells and T cells in the development and recovery of SAE and mental impairment following sepsis.