Neutralizing anti-interleukin-1β antibodies modulate fetal blood-brain barrier function after ischemia
Document Type
Article
Date of Original Version
1-1-2015
Abstract
We have previously shown that increases in blood-brain barrier permeability represent an important component of ischemia-reperfusion related brain injury in the fetus. Pro-inflammatory cytokines could contribute to these abnormalities in blood-brain barrier function. We have generated pharmacological quantities of mouse anti-ovine interleukin-1β monoclonal antibody and shown that this antibody has very high sensitivity and specificity for interleukin-1β protein. This antibody also neutralizes the effects of interleukin-1β protein in vitro. In the current study, we hypothesized that the neutralizing anti-interleukin-1β monoclonal antibody attenuates ischemia-reperfusion related fetal blood-brain barrier dysfunction. Instrumented ovine fetuses at 127. days of gestation were studied after 30. min of carotid occlusion and 24. h of reperfusion. Groups were sham operated placebo-control- (n. =. 5), ischemia-placebo- (n. =. 6), ischemia-anti-IL-1β antibody- (n. =. 7), and sham-control antibody- (n. =. 2) treated animals. Systemic infusions of placebo (0.154. M NaCl) or anti-interleukin-1β monoclonal antibody (5.1. ±. 0.6. mg/kg) were given intravenously to the same sham or ischemic group of fetuses at 15. min and 4. h after ischemia. Concentrations of interleukin-1β protein and anti-interleukin-1β monoclonal antibody were measured by ELISA in fetal plasma, cerebrospinal fluid, and parietal cerebral cortex. Blood-brain barrier permeability was quantified using the blood-to-brain transfer constant (. Ki) with α-aminoisobutyric acid in multiple brain regions. Interleukin-1β protein was also measured in parietal cerebral cortices and tight junction proteins in multiple brain regions by Western immunoblot. Cerebral cortical interleukin-1β protein increased (. P<. 0.001) after ischemia-reperfusion. After anti-interleukin-1β monoclonal antibody infusions, plasma anti-interleukin-1β monoclonal antibody was elevated (. P<. 0.001), brain anti-interleukin-1β monoclonal antibody levels were higher (. P<. 0.03), and interleukin-1β protein concentrations (. P<. 0.03) and protein expressions (. P<. 0.001) were lower in the monoclonal antibody-treated group than in placebo-treated-ischemia-reperfusion group. Monoclonal antibody infusions attenuated ischemia-reperfusion-related increases in Ki across the brain regions (. P<. 0.04), and Ki showed an inverse linear correlation (r. = -. 0.65, P<. 0.02) with anti-interleukin-1β monoclonal antibody concentrations in the parietal cortex, but had little effect on tight junction protein expression. We conclude that systemic anti-interleukin-1β monoclonal antibody infusions after ischemia result in brain anti-interleukin-1β antibody uptake, and attenuate ischemia-reperfusion-related interleukin-1β protein up-regulation and increases in blood-brain barrier permeability across brain regions in the fetus. The pro-inflammatory cytokine, interleukin-1β, contributes to impaired blood-brain barrier function after ischemia in the fetus.
Publication Title, e.g., Journal
Neurobiology of Disease
Volume
73
Citation/Publisher Attribution
Chen, Xiaodi, Grazyna B. Sadowska, Jiyong Zhang, Jeong Eun Kim, Erin E. Cummings, Courtney A. Bodge, Yow Pin Lim, Oleksandr Makeyev, Walter G. Besio, John Gaitanis, Steven W. Threlkeld, William A. Banks, and Barbara S. Stonestreet. "Neutralizing anti-interleukin-1β antibodies modulate fetal blood-brain barrier function after ischemia." Neurobiology of Disease 73, (2015). doi: 10.1016/j.nbd.2014.09.007.