4.6 Article

TNF-α antagonism rescues the effect of ageing on stroke: Perspectives for targeting inflamm-ageing

Journal

Publisher

WILEY
DOI: 10.1111/eci.13600

Keywords

ageing; inflamm-ageing; inflammation; ischaemic stroke; matrix metalloproteinases; TNF alpha

Funding

  1. Swiss National Science Foundation [310030_197510]
  2. Swiss Heart Foundation
  3. Alfred and Annemarie von Sick Grants for Translational and Clinical Research Cardiology and Oncology
  4. Foundation for Cardiovascular Research-Zurich Heart House
  5. Sheikh Khalifa's Foundation Assistant Professorship at the Faculty of Medicine, University of Zurich
  6. US National Heart, Lung and Blood Institute [R01HL080472, 1R01HL134892]
  7. American Heart Association [18CSA34080399]
  8. RRM and Simard Charitable Funds
  9. Swiss National Science Foundation (SNF) [310030_197510] Funding Source: Swiss National Science Foundation (SNF)

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Older mice showed larger stroke size and increased neuromotor deficit compared to young ones. Inhibition of TNF-alpha restored stroke volume, neuromotor performance, and survival rates in older mice, suggesting TNF-alpha as a causative contributor to the deleterious effect of aging on stroke outcomes. Increased TNF-alpha plasma levels in patients with ischemic stroke correlated with worsened short-term neurological outcome and age.
Aims: Epidemiologic evidence links ischemic stroke to age, yet the mechanisms that underlie the specific and independent effects of age on stroke remain elusive, impeding the development of targeted treatments. This study tested the hypothesis that age directly aggravates stroke outcomes and proposes inflamm-aging as a mediator and potential therapeutic target. Methods: 3 months- (young) and 18-20 months-old (old) mice underwent transient middle cerebral artery occlusion (tMCAO) for 30 minutes followed by 48 hours of reperfusion. Old animals received weekly treatment with the TNF-alpha neutralizing antibody adalimumab over 4 weeks before tMCAO in a separate set of experiments. Plasma levels of TNF- alpha were assessed in patients with ischemic stroke and correlated with age and outcome. Results: Old mice displayed larger stroke size than young ones with increased neuromotor deficit. Immunohistochemical analysis revealed impairment of the blood-brain barrier in old mice, i.e. increased post-stroke degradation of endothelial tight junctions and expression of tight junctions-digesting and neurotoxic matrix metalloproteinases. At baseline, old animals showed a broad modulation of several circulating inflammatory mediators. TNF-alpha displayed the highest increase in old animals and its inhibition restored the volume of stroke, neuromotor performance, and survival rates of old mice to the levels observed in young ones. Patients with ischemic stroke showed increased TNF-alpha plasma levels which correlated with worsened short-term neurological outcome as well as with age. Conclusions: This study identifies TNF-alpha as a causative contributor to the deleterious effect of aging on stroke and points to inflamm-aging as a mechanism of age-related worsening of stroke outcomes and potential therapeutic target in this context. Thus, this work provides a basis for tailoring novel stroke therapies for the particularly vulnerable elderly population.

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