Safety of multiple administrations of spermicidal LL-37 antimicrobial peptide into the mouse female reproductive

Seung Gee Lee1, Wongsakorn Kiattiburut1, Stephanie C Burke Schinkel1

  • 1Chronic Disease Program, Ottawa Hospital Research Institute, Ottawa, ON, Canada.

PubMed

Insights

Repeated administration of LL-37 antimicrobial peptide in female mice did not cause reproductive tract damage or impair fertility. This supports LL-37

Area of Science:

  • Reproductive biology and immunology
  • Antimicrobial peptide research
  • Contraceptive development

Background:

  • LL-37 antimicrobial peptide exhibits spermicidal and microbicidal properties.
  • LL-37 is a candidate for a multipurpose prevention technology (MPT) for the female reproductive tract (FRT).
  • Safety of repeated LL-37 administration in the FRT requires investigation to prevent tissue damage and infertility.

Purpose of the Study:

  • To evaluate the safety of multiple transcervical administrations of LL-37 in female mice.
  • To assess potential damage to the vagina, cervix, and uterus after repeated LL-37 exposure.
  • To determine if repeated LL-37 administration affects the resumption of fecundity.

Main Methods:

  • Female mice received transcervical injections of LL-37 (10× spermicidal dose) over three consecutive estrous cycles.
  • Histological assessments of reproductive tissues were performed 24 hours post-injection.
  • Pregnancy rates were monitored after artificial insemination one week post-injection.
  • Controls included PBS (negative) and nonoxynol-9 vaginal contraceptive foam (positive).

Main Results:

  • LL-37 and PBS injections resulted in normal histology of the vagina, cervix, and uterus.
  • Mice treated with LL-37 or PBS showed 100% resumption of fecundity.
  • Vaginal contraceptive foam (nonoxynol-9) caused histological abnormalities and reduced fecundity to 50%.

Conclusions:

  • Multiple intravaginal administrations of LL-37 are safe in the mouse model, causing no FRT tissue damage or loss of fertility.
  • LL-37 demonstrates potential as a safe agent for vaginal MPTs.
  • Further studies in non-human primates and humans are necessary to confirm safety and efficacy.

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