Inhibition of infection‐mediated preterm birth by administration of broad spectrum chemokine inhibitor in mice

• Published in: Journal of cellular and molecular medicine Vol. 18; no. 9; pp. 1816 - 1829
• Main Authors: Shynlova, Oksana, Dorogin, Anna, Li, Yunqing, Lye, Stephen
• Format: Journal Article
• Language: English
• Published: England John Wiley & Sons, Inc 01.09.2014; Blackwell Publishing Ltd
• Subjects: Amniotic fluid; Animals; Anti-Inflammatory Agents - pharmacology; Birth; chemokine inhibitor; Chemokines; Chemokines - antagonists & inhibitors; Chemokines - genetics; Chemokines - metabolism; Cytokines; Decidua; Disease; Drug dosages; Ethanol; Female; Gene expression; HIV; Human immunodeficiency virus; Humans; Immune system; Immunohistochemistry; Infant mortality; infection; Infections; Inflammation; Injection; leucocyte infiltration; Lipopolysaccharides; Lipopolysaccharides - pharmacology; Mice; Mice, Inbred ICR; Myometrium; Myometrium - drug effects; Myometrium - immunology; Neonates; Neutrophil Infiltration; Original; Placenta; Pregnancy; Pregnancy Complications, Infectious - drug therapy; Premature birth; Premature Birth - immunology; Premature Birth - prevention & control; preterm labour; Tissues; Tropical diseases; Tumor necrosis factor-TNF; Uterus; Uterus - drug effects; Uterus - immunology; leucocyte infiltration; infection; preterm labour; uterus; chemokine inhibitor
• ISSN: 1582-1838; 1582-4934
• DOI: 10.1111/jcmm.12307

Preterm birth (PTB) is the single most important cause of perinatal and infant mortality worldwide. Maternal infection can result in PTB. We investigated the ability of a Broad Spectrum Chemokine Inhibitor (BSCI) to prevent infection‐induced PTB in mice. PTB was initiated in pregnant mice by intraperitoneal injection of lipopolysaccharide (LPS; 50 μg). Half the mice received BSCI (10 mg/kg) 24 hrs prior to and immediately before LPS administration. The impact of LPS alone or LPS plus BSCI was assessed on (i) injection‐to‐delivery interval, foetal survival rate, placental and neonates' weight; (ii) amniotic fluid and maternal plasma cytokine levels (by Luminex assay); foetal and maternal tissue cytokine gene expression levels (by Real‐Time RT‐PCR); (iii) immune cells infiltration into the uterine tissue (by stereological immunohistochemistry). Pre‐treatment with BSCI (i) decreased LPS‐induced PTB (64% versus 100%, P < 0.05); (ii) significantly attenuated cytokine/chemokine expression in maternal tissues (plasma, liver, myometrium, decidua); (iii) significantly decreased neutrophil infiltration in the mouse myometrium. BSCI‐treated mice in which PTB was delayed till term had live foetuses with normal placental and foetal weight. BSCI represents a promising new class of therapeutics for PTB. In a mouse model of preterm labour, BCSI suppresses systemic inflammation in maternal tissues which resulted in the reduced incidence of LPS‐mediated PTB. These data provide support for efforts to target inflammatory responses as a means of preventing PTB.