Literature DB >> 29889085

T-cell infiltration into the perilesional cortex is long-lasting and associates with poor somatomotor recovery after experimental traumatic brain injury.

Xavier Ekolle Ndode-Ekane1, Liz Matthiesen1, Ivette Bañuelos-Cabrera1, Cátia Alexandra Pêgas Palminha1, Asla Pitkänen1.   

Abstract

BACKGROUND: T-lymphocyte (T-cell) invasion into the brain parenchyma is a major consequence of traumatic brain injury (TBI). However, the role of T-cells in the post-TBI functional outcome and secondary inflammatory processes is unknown. We explored the dynamics of T-cell infiltration into the cortex after TBI to establish whether the infiltration relates to post-injury functional impairment/recovery and progression of the secondary injury.
METHOD: TBI was induced in rats by lateral fluid-percussion injury, and the acute functional impairment was assessed using the neuroscore. Animals were killed between 1-90 d post-TBI for immunohistochemical analysis of T-cell infiltration (CD3), chronic macrophage/microglial reaction (CD68), blood-brain barrier (BBB) dysfunction (IgG), and endophenotype of the cortical injury. Furthermore, the occurrence of spontaneous seizures and spike-and-wave discharges were assessed using video-electroencephalography.
RESULTS: The number of T-cells peaked at 2-d post-TBI, and then dramatically decreased by 7-d post-TBI (5% of 2-d value). Unexpectedly, chronic T-cell infiltration at 1 or 3 months post-TBI did not correlate with the severity of chronic inflammation (p > 0.05) or BBB dysfunction (p > 0.05). Multiple regression analysis indicated that inflammation and BBB dysfunction is associated with 48% of the perilesional T-cell infiltration even at the chronic time-point (r = 0.695, F = 6.54, p < 0.05). The magnitude of T-cell infiltration did not predict the pathologic endophenotype of cortical injury, but the higher the number of T-cells in the cortex, the poorer the recovery index based on the neuroscore (r = - 0.538, p < 0.05). T-cell infiltration was not associated with the number or duration of age-related spike-and-wave discharges (SWD). Nevertheless, the higher the number of SWD, the poorer the recovery index (r = - 0.767, p < 0.5).
CONCLUSIONS: These findings suggest that acute infiltration of T-cells into the brain parenchyma after TBI is a contributing factor to poor post-injury recovery.

Entities:  

Keywords:  Fluid-percussion brain injury; T-lymphocytes; functional impairment; inflammation; traumatic brain injury

Mesh:

Substances:

Year:  2018        PMID: 29889085     DOI: 10.3233/RNN-170811

Source DB:  PubMed          Journal:  Restor Neurol Neurosci        ISSN: 0922-6028            Impact factor:   2.406


  7 in total

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4.  Astrocyte-targeted Overproduction of IL-10 Reduces Neurodegeneration after TBI.

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5.  Reorganization of Thalamic Inputs to Lesioned Cortex Following Experimental Traumatic Brain Injury.

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6.  Chronic Regulation of miR-124-3p in the Perilesional Cortex after Experimental and Human TBI.

Authors:  Niina Vuokila; Eleonora Aronica; Anatoly Korotkov; Erwin Alexander van Vliet; Salma Nuzhat; Noora Puhakka; Asla Pitkänen
Journal:  Int J Mol Sci       Date:  2020-03-31       Impact factor: 5.923

Review 7.  Revisiting Excitotoxicity in Traumatic Brain Injury: From Bench to Bedside.

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Journal:  Pharmaceutics       Date:  2022-01-08       Impact factor: 6.321

  7 in total

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