Taiwanese Journal of Obstetrics & Gynecology (Jun 2005)

Potential of Lactoferrin in the Prevention of Preterm Delivery

  • Katsufumi Otsuki,
  • Akitoshi Hasegawa,
  • Yasushi Sasaki,
  • Maki Sawada,
  • Kyoko Yakuwa,
  • Kaori Mitsukawa,
  • Hiroshi Chiba,
  • Masaaki Nagatsuka,
  • Takashi Okai

DOI
https://doi.org/10.1016/S1028-4559(09)60123-6
Journal volume & issue
Vol. 44, no. 2
pp. 123 – 127

Abstract

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Objective: Chorioamnionitis (CAM), an ascending infection from maternal bacterial vaginosis or cervicitis, can cause preterm delivery. We hypothesized that lactoferrin (LF), in particular recombinant human LF (rh-LF), may prevent preterm delivery. We conducted three experiments to demonstrate LF's ability to prevent preterm delivery. Materials and Methods: First, we correlated human cervical mucus LF concentration and LF and interleukin- 6 (IL-6) concentrations in amniotic fluid to gestational weeks, in mothers with and without CAM. Second, using an amnion cell culture system, we studied the preventive effect of rh-LF on inflammatory cytokine production induced by lipopolysaccharide. Using human cervical gland cell lines, we studied the preventive effects of rh-LF on the growth of Escherichia coli. Thirdly, we studied the preventive effect of rh-LF in mouse and rabbit models of preterm delivery. We also examined LF's preventive effect on the production of inflammatory cytokines in maternal serum and amniotic fluid. Results: In mothers with CAM, amniotic fluid LF concentrations were elevated and IL-6 production increased as fetal LF levels and inflammation increased. LF administration prevented IL-6 production, demonstrating LF's anti-cytokine action and control over E. coli. Length of pregnancy was extended and fetal survival rates were higher in mothers who received LF. Conclusion: It appears that LF is highly beneficial in the prevention of preterm delivery and improving poor fetal prognosis due to elevated inflammatory cytokine levels. Specifically, rh-LF may prevent the production of inflammatory cytokines under E. coli infection or control maternal cytokine production.

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