Placental viral infection sensitizes to endotoxin‐induced pre‐term labor: a double hit hypothesis
American journal of reproductive immunology, 2011•Wiley Online Library
Citation Cardenas I, Mor G, Aldo P, Lang SM, Stabach P, Sharp A, Romero R, Mazaki‐Tovi
S, Gervasi MTeresa, Means RE. Placental viral infection sensitizes to endotoxin‐induced pre‐
term labor: a double hit hypothesis. Am J Reprod Immunol 2011; 65: 110–117 Problem
Among pregnant women, acquired viral infections with a concurrent bacterial infection is a
detrimental factor associated to poor prognosis. We evaluate the effect of a viral infection
that does not lead to pre‐term labor on the response to low doses of lipopolysaccharide …
S, Gervasi MTeresa, Means RE. Placental viral infection sensitizes to endotoxin‐induced pre‐
term labor: a double hit hypothesis. Am J Reprod Immunol 2011; 65: 110–117 Problem
Among pregnant women, acquired viral infections with a concurrent bacterial infection is a
detrimental factor associated to poor prognosis. We evaluate the effect of a viral infection
that does not lead to pre‐term labor on the response to low doses of lipopolysaccharide …
Citation Cardenas I, Mor G, Aldo P, Lang SM, Stabach P, Sharp A, Romero R, Mazaki‐Tovi S, Gervasi MTeresa, Means RE. Placental viral infection sensitizes to endotoxin‐induced pre‐term labor: a double hit hypothesis. Am J Reprod Immunol 2011; 65: 110–117
Problem Among pregnant women, acquired viral infections with a concurrent bacterial infection is a detrimental factor associated to poor prognosis. We evaluate the effect of a viral infection that does not lead to pre‐term labor on the response to low doses of lipopolysaccharide (LPS). Our objectives were (i) to characterize the effect of a viral infection concurrent with exposure to microbial products on pregnancy outcome and (ii) to characterize the placental and fetal immune responses to the viral sensitization to LPS.
Method C57B/6 wild‐type mice were injected with murine gammaherpesvirus 68 (MHV68) at E8.5. Either PBS or LPS was injected i.p. at E15.5. Pregnancy outcome and cytokine/chemokine profile from implantation sites were analyzed by multiplex.
Results LPS treatment of MHV‐68‐infected animals induced pre‐term delivery and fetal death in 100% of the mice. Pre‐term labor was characterized by a upregulation of pro‐inflammatory cytokines and chemokines in both placenta and decidua. Similar profiles were observed from MHV‐68‐infected human primary trophoblast and trophoblast cell lines in response to LPS.
Conclusion We describe for the first time that a sub‐clinical viral infection in pregnant mice might sensitize to a bacterial infection leading to pre‐term delivery. We propose the ‘Double Hit Hypothesis’ where the presence of a viral infection enhances the effect of bacterial products during pregnancy leading not only to pre‐term labor but likely larger adverse outcomes.
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