Evidence map›Paper›PMID 37326833›Full record

ArticleMolecular human reproduction2023

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

Seung Gee Lee, Wongsakorn Kiattiburut, Stephanie C Burke Schinkel, Jonathan Angel, Nongnuj Tanphaichitr

Open access · bronzeAbstract read
In one paragraph

Article in Molecular human reproduction, 2023. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 1 paper.

0numbers the graph read from it
0cells of the map it votes in
1citing papers in PubMed
0.6field-weighted citation impact, top 36% of its field
1 · What the graph read from it

What it found

Each row is one number read from the abstract, on the scale the paper reported it, with its interval. Left of the dashed line favours the treatment, right favours the comparator. Under each row is the sentence it came from. New to these charts? A ten-minute tutorial.

The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.

2 · The registry

The trial behind it

Trials whose registry record cites this paper, or whose number appears in the abstract. A trial that started after this paper was published is citing it as background, not reporting it.

Neither the registry nor the abstract names a trial number. If this is a trial report, that itself is worth knowing.

3 · Its place in the literature

Who cites it

1 citing paper in PubMed, 3 citations in OpenAlex.

  1. Review
4 · The record

Corrections and comments

PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.

5 · Who and what money

Authors and funding

5 authors at 2 institutions in 1 country.

Seung Gee LeeChronic Disease Program, Ottawa Hospital Research Institute, Ottawa, ON, Canada.
Wongsakorn KiattiburutChronic Disease Program, Ottawa Hospital Research Institute, Ottawa, ON, Canada.
Stephanie C Burke SchinkelChronic Disease Program, Ottawa Hospital Research Institute, Ottawa, ON, Canada.
Jonathan AngelChronic Disease Program, Ottawa Hospital Research Institute, Ottawa, ON, Canada.
Nongnuj TanphaichitrChronic Disease Program, Ottawa Hospital Research Institute, Ottawa, ON, Canada.ORCID 0000-0002-8585-6670
Ottawa Hospital · CAUniversity of Ottawa · CA

Funding

CIHR PJT 173268
6 · The paper itself

Abstract

We have previously demonstrated spermicidal activity of LL-37 antimicrobial peptide on mouse/human sperm and its contraceptive effects in female mice. With its microbicidal action against Neisseria gonorrhoeae, LL-37 warrants development into a multipurpose prevention technology (MPT) agent for administering into the female reproductive tract (FRT). However, it is important to verify that multiple administrations of LL-37 do not lead to damage of FRT tissues and/or irreversible loss of fecundity. Herein, we transcervically injected LL-37 (36 µM-10× spermicidal dose) into female mice in estrus in three consecutive estrous cycles. A set of mice were sacrificed for histological assessment of the vagina/cervix/uterus 24 h after the last injection, while the second set were artificially inseminated with sperm from fertile males 1 week afterwards, and then monitored for pregnancy. Mice injected with PBS in parallel were regarded as negative controls, whereas those injected with vaginal contraceptive foam (VCF, available over the counter), containing 12.5% nonoxynol-9, served as positive controls for vaginal epithelium disruption. We demonstrated that the vagina/cervix/uterus remained normal in both LL-37-injected and PBS-injected mice, which also showed 100% resumption of fecundity. In contrast, VCF-injected mice showed histological abnormalities in the vagina/cervix/uterus and only 50% of them resumed fecundity. Similarly, LL-37 multiply administered intravaginally caused no damage to FRT tissues. While our results indicate the safety of multiple treatments of LL-37 in the mouse model, similar studies have to be conducted in non-human primates and then humans. Regardless, our study provides an experimental model for studying in vivo safety of other vaginal MPT/spermicide candidates.

Indexed as

Antimicrobial PeptidesSpermatocidal AgentsAnimalsFemaleHumansMaleMiceNonoxynolPregnancySemenSpermatozoaAntimicrobial PeptidesNonoxynolSpermatocidal Agentsantimicrobial peptidecytokines/chemokinesfecundityfemale reproductive tractLL-37multipurpose prevention technologynonoxynol-9spermicidevaginal epitheliumvaginal microbicide

Identifiers

PMID37326833
PMCPMC10323174
OpenAlexW4380869848

What OpenQuestion holds

Textmetadata
Read underepoch 390

Registered trials

None linked

Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.