According to a new study, inflammation from bacterial infections is linked to pre-term births and deaths. Researchers from Case Western Reserve University's School of Dental Medicine and the Case School of Medicine have found that receptors responding to the presence of dead or living bacteria in the placentas of mice can be blocked, the number of pre-term deaths will decline by nearly half.
"New findings from the mouse study holds potential to develop ways to curb the emotional and economic toll on families that lose babies to pre-term labour and foetal death," said Yiping Han, a member of from the department of periodontics.
Currently antibiotic treatments are not very effective at preventing pre-term births that are triggered by a bacterial infection. Mice, as well as humans, have several toll-like receptors (TLR) that sense the surface components of living or dead bacteria. TLR2 and 4 are key receptors in recognizing bacterial surfaces. The investigators concentrated their study on these two receptors as a possible link in producing the inflammatory response that is believed to have brought about the foetal death in mice.
In a prior mouse study at Case Western Reserve, the investigators noted that inflammation closely paralleled localization of bacteria. In the present study, the researchers found that mice deficient in TLR4 lacked the necro-inflammatory response to bacteria and produced healthy pups. This discovery led Han and her colleagues to attempt to block the inflammatory process by using synthetic TLR4 antagonist that prevented the receptor from sensing the bacteria.
Fusobacterium nucleatum, a common oral pathogen also found in the amniotic fluid of pre-term babies, was used as the model organism for the study. Around day 16 of the gestation period for the mice (the equivalent of the third trimester for humans), F. nucleatum was injected into three groups of mice-one that had TLR4 receptors, a group of TLR4-deficient mice and a group that had TLR4 receptors but were given a synthetic compound to block the receptor's inflammatory response. Within eighteen hours, inflammation was present in the TLR4 mice.
"F. nucleatum colonization in the mouse placenta was accompanied by inflammation, similar to intrauterine infection in humans, suggesting placental inflammatory response as an important factor in the pathogenesis of bacterial-inducted pre-term birth," The researchers wrote.
Han said the synthetic TLR4 antagonist appears to be safe for mice mothers and their pups.
The study is published in the Journal of Immunology.