Role of T lymphocytes and interferon-gamma in ischemic stroke.

TLDR: Findings indicate that CD4+ and CD8+ T lymphocytes, but not B lymphocyte, contribute to the inflammatory and thrombogenic responses, brain injury, and neurological deficit associated with experimental stroke.

Abstract: Background— Although lymphocyte recruitment and activation are associated with cerebral ischemia-reperfusion (I/R) injury, the contributions of specific lymphocyte subpopulations and lymphocyte-derived interferon-γ (IFN-γ) to stroke remain unknown. The objectives of this study were to define the contribution of specific populations of lymphocytes to the inflammatory and prothrombogenic responses elicited in the cerebral microvasculature by I/R and to investigate the role of T-cell–associated IFN-γ in the pathogenesis of ischemic stroke. Methods and Results— Middle cerebral artery occlusion was induced for 1 hour (followed by 4 or 24 hours of reperfusion) in wild-type mice and mice deficient in lymphocytes (Rag1−/−), CD4+ T cells, CD8+ T cells, B cells, or IFN-γ. Platelet and leukocyte adhesion was assessed in cortical venules with intravital video microscopy. Neurological deficit and infarct volume were determined 24 hours after reperfusion. Rag1−/−, CD4+ T-cell−/−, CD8+ T-cell−/−, and IFN-γ−/− mice exhib...