Please use this identifier to cite or link to this item: http://hdl.handle.net/2440/107115
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Type: Journal article
Title: Antenatal suppression of il-1 protects against inflammation-induced fetal injury and improves neonatal and developmental outcomes in mice
Author: Nadeau-Vallée, M.
Chin, P.
Belarbi, L.
Brien, M.
Pundir, S.
Berryer, M.
Beaudry-Richard, A.
Madaan, A.
Sharkey, D.
Lupien-Meilleur, A.
Hou, X.
Quiniou, C.
Beaulac, A.
Boufaied, I.
Boudreault, A.
Carbonaro, A.
Doan, N.
Joyal, J.
Lubell, W.
Olson, D.
et al.
Citation: Journal of Immunology, 2017; 198(5):2047-2062
Publisher: American Association of Immunologists
Issue Date: 2017
ISSN: 0022-1767
1550-6606
Statement of
Responsibility: 
Mathieu Nadeau-Vallée, Peck-Yin Chin, Lydia Belarbi, Marie-Ève Brien, Sheetal Pundir, Martin H. Berryer, Alexandra Beaudry-Richard, Ankush Madaan, David J. Sharkey, Alexis Lupien-Meilleur, Xin Hou, Christiane Quiniou, Alexandre Beaulac, Ines Boufaied, Amarilys Boudreault, Adriana Carbonaro, Ngoc-Duc Doan, Jean-Sebastien Joyal, William D. Lubell, David M. Olson, Sarah A. Robertson, Sylvie Girard and Sylvain Chemtob
Abstract: Preterm birth (PTB) is commonly accompanied by in utero fetal inflammation, and existing tocolytic drugs do not target fetal inflammatory injury. Of the candidate proinflammatory mediators, IL-1 appears central and is sufficient to trigger fetal loss. Therefore, we elucidated the effects of antenatal IL-1 exposure on postnatal development and investigated two IL-1 receptor antagonists, the competitive inhibitor anakinra (Kineret) and a potent noncompetitive inhibitor 101.10, for efficacy in blocking IL-1 actions. Antenatal exposure to IL-1β induced Tnfa, Il6, Ccl2, Pghs2, and Mpges1 expression in placenta and fetal membranes, and it elevated amniotic fluid IL-1β, IL-6, IL-8, and PGF2α, resulting in PTB and marked neonatal mortality. Surviving neonates had increased Il1b, Il6, Il8, Il10, Pghs2, Tnfa, and Crp expression in WBCs, elevated plasma levels of IL-1β, IL-6, and IL-8, increased IL-1β, IL-6, and IL-8 in fetal lung, intestine, and brain, and morphological abnormalities: e.g., disrupted lung alveolarization, atrophy of intestinal villus and colon-resident lymphoid follicle, and degeneration and atrophy of brain microvasculature with visual evoked potential anomalies. Late gestation treatment with 101.10 abolished these adverse outcomes, whereas Kineret exerted only modest effects and no benefit for gestation length, neonatal mortality, or placental inflammation. In a LPS-induced model of infection-associated PTB, 101.10 prevented PTB, neonatal mortality, and fetal brain inflammation. There was no substantive deviation in postnatal growth trajectory or adult body morphometry after antenatal 101.10 treatment. The results implicate IL-1 as an important driver of neonatal morbidity in PTB and identify 101.10 as a safe and effective candidate therapeutic.
Keywords: Brain; Placenta; Animals; Mice, Inbred C57BL; Animals, Newborn; Humans; Mice; Premature Birth; Disease Models, Animal; Inflammation; Lipopolysaccharides; Peptides; Inflammation Mediators; Fetal Development; Pregnancy; Female; Interleukin 1 Receptor Antagonist Protein; Interleukin-1beta
Rights: © 2017 by The American Association of Immunologists, Inc. All rights reserved.
RMID: 0030063847
DOI: 10.4049/jimmunol.1601600
Appears in Collections:Medicine publications

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