Evidence map›Paper›PMID 25875100›Full record

ArticlePloS one2015

Robust vaginal colonization of macaques with a novel vaginally disintegrating tablet containing a live biotherapeutic product to prevent HIV infection in women.

Laurel A Lagenaur, Iwona Swedek, Peter P Lee, Thomas P Parks

Open access · goldAbstract read
In one paragraph

Article in PloS one, 2015. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 16 papers.

0numbers the graph read from it
0cells of the map it votes in
16citing papers in PubMed
1.8field-weighted citation impact, top 16% 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

16 citing papers in PubMed, 23 citations in OpenAlex.

  1. Review
  2. Review
  3. Review
  4. Article
  5. Microbiome Studies in Non-human Primates.Current HIV/AIDS reports · 2021
    Review
  6. Review
  7. Review
  8. Review
  9. Review
  10. Review
  11. Article
  12. On-demand microbicide products: design matters.Drug delivery and translational research · 2017
    Review
  13. A Summary of the Second Annual HIV Microbiome Workshop.AIDS research and human retroviruses · 2017
    Article
  14. Article
  15. Article
  16. mSphere
    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

4 authors at 2 institutions in 1 country.

Laurel A LagenaurOsel, Inc., Mountain View, California, United States of America; Vaccine Branch, National Cancer Institute, National Institutes of Health, Bethesda, Maryland, United States of America.
Iwona SwedekOsel, Inc., Mountain View, California, United States of America.
Peter P LeeOsel, Inc., Mountain View, California, United States of America.
Thomas P ParksOsel, Inc., Mountain View, California, United States of America.
Osel (United States) · USNational Institutes of Health · US

Funding

Delivery of passive immunity against HIV using commensal vaginal Lactobacillus bioengineered to secrete broadly neutralizing domain antibodiesR44AI100753 · NIAID · OSEL, INC. · PI LAGENAUR, LAUREL A. · 2014 to 2015
$2.7M
Development of a Live Topical Microbicide for WomenR33AI071978 · NIAID · OSEL, INC. · PI LAGENAUR, LAUREL A. · 2009 to 2011
$1.5M
NIAID NIH HHS 5R33AI071978NIAID NIH HHS R33 AI071978NIAID NIH HHS R44 AI100753
6 · The paper itself

Abstract

MucoCept is a biotherapeutic for prevention of HIV-1 infection in women and contains a human, vaginal Lactobacillus jensenii that has been genetically enhanced to express the HIV-1 entry inhibitor, modified cyanovirin-N (mCV-N). The objective of this study was to develop a solid vaginal dosage form that supports sustained vaginal colonization of the MucoCept Lactobacillus at levels previously shown, with freshly prepared cultures, to protect macaques from SHIV infection and to test this formulation in a macaque vaginal colonization model. Vaginally disintegrating tablets were prepared by lyophilizing the formulated bacteria in tablet-shaped molds, then packaging in foil pouches with desiccant. Disintegration time, potency and stability of the tablets were assessed. For colonization, non-synchronized macaques were dosed vaginally with either one tablet or five tablets delivered over five days. Vaginal samples were obtained at three, 14, and 21 days post-dosing and cultured to determine Lactobacillus colonization levels. To confirm identity of the MucoCept Lactobacillus strain, genomic DNA was extracted from samples on days 14 and 21 and a strain-specific PCR was performed. Supernatants from bacteria were tested for the presence of the mCV-N protein by Western blot. The tablets were easy to handle, disintegrated within two minutes, potent (5.7x1011 CFU/g), and stable at 4°C and 25°C. Vaginal administration of the tablets to macaques resulted in colonization of the MucoCept Lactobacillus in 66% of macaques at 14 days post-dosing and 83% after 21 days. There was no significant difference in colonization levels for the one or five tablet dosing regimens (p=0.88 Day 14, p=0.99 Day 21). Strain-specific PCR confirmed the presence of the bacteria even in culture-negative macaques. Finally, the presence of mCV-N protein was confirmed by Western blot analysis using a specific anti-mCV-N antibody.

Indexed as

Organisms, Genetically ModifiedAdministration, IntravaginalAdultAnimalsBacterial ProteinsCarrier ProteinsColony Count, MicrobialFemaleGene ExpressionHIV-1HIV InfectionsHumansLactobacillusMacaca mulattaPolymerase Chain ReactionSimian Immunodeficiency VirusBacterial ProteinsCarrier Proteinscyanovirin NTablets

Identifiers

PMID25875100
PMCPMC4397015
OpenAlexW2074208355

What OpenQuestion holds

Textmetadata
LicenceCC BY
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.