Key result
Acute stroke is linked to sharply elevated IL-10-secreting blood mononuclear cells versus healthy controls.
Case-Control
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Ischemic stroke is associated with altered systemic immune responses both early after the onset and in the recovery phase. Interleukin (IL)-10, a Th2 related cytokine, has multiple effects on different cell types, including T and B lymphocytes, monocytes, neutrophils and mast cells. IL-4 is another Th2 cytokine that inhibits the synthesis of pro-inflammatory cytokines by Th1 clones. We used enzyme-linked immunospot assays to detect and enumerate blood mononuclear cells (MNC) secreting IL-10 and IL-4 spontaneously as well as after stimulation with myelin basic protein (MBP), considered to be an autoantigen of possible pathogenic importance in, for example, multiple sclerosis, to evaluate the involvement of anti-inflammatory cytokines in ischemic stroke. All patients with ischemic stroke and cerebral hemorrhage had strongly elevated numbers of IL-10 secreting blood MNC compared with healthy individuals. Numbers of MBP-reactive IL-10 secreting blood MNC were also elevated in a proportion of the patients with stroke and hemorrhage. Levels of IL-4 secreting blood MNC did not differ in ischemic stroke versus healthy individuals. The anti-inflammatory IL-10 could play a pivotal role in ischemic stroke as well as cerebral hemorrhage.
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Pelidou et al. (1999) conducted a case-control in Ischemic stroke and cerebral hemorrhage. Cerebrovascular disease (ischemic stroke and cerebral hemorrhage) vs. Healthy individuals was evaluated on Number of IL-10 and IL-4 secreting blood mononuclear cells. Patients with ischemic stroke and cerebral hemorrhage had strongly elevated numbers of IL-10 secreting blood mononuclear cells compared with healthy individuals.
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