ArticleFrontiers in immunology2026
Friend or foe: divergent immunomodulatory effects of metabolites derived from the virucidal zinc finger inhibitor SAMT-247.
Article in Frontiers in immunology, 2026. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.
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.
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.
Who cites it
0 citing papers in PubMed.
No citing paper in PubMed yet.
Corrections and comments
PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.
Authors and funding
17 authors.
Funding
No grant is acknowledged in the PubMed record.
Abstract
Background: Topical administration of SAMT-247, a mercaptobenzamide thioester zinc finger inhibitor targeting the HIV nucleocapsid Gag zinc finger protein, generates multiple metabolites in mucosal tissues, including Met-A, Met-B, Met-C, and Met-D. Prior studies established that SAMT-247, delivered either as a vaginal gel or via an intravaginal ring (IVR), synergizes with the ΔV1DNA/ALVAC-SIV/ΔV1gp120/alum vaccine regimen to markedly reduce vaginal SIV Methods: We performed Results: High concentrations of Met-B, Met-C, and Met-D were detected in vaginal secretions, whereas vaginal tissues contained predominantly Met-D, low levels of Met-A, and no detectable Met-B or Met-C. Functionally, Met-D most closely recapitulated and reinforced the protective immune profile associated with SAMT-247, preserving or expanding IL-17 Conclusion: We observed distinct immunomodulatory effects associated with different SAMT-247 metabolites. These findings may guide future delivery strategies that favor tissue-available Met-D while limiting Met-A accumulation. More broadly, this study underscores the importance of metabolite-specific analyses for defining the biological activity and mechanisms of action of therapeutic agents.
Indexed as
Identifiers
What OpenQuestion holds
Registered trials
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.