Evidence map›Paper›PMID 25422427›Full record

ArticleProceedings of the National Academy of Sciences of the United States of America2014

In vivo treatment of Helicobacter pylori infection with liposomal linolenic acid reduces colonization and ameliorates inflammation.

Soracha Thamphiwatana, Weiwei Gao, Marygorret Obonyo, Liangfang Zhang

Open access · bronzeAbstract read
In one paragraph

Article in Proceedings of the National Academy of Sciences of the United States of America, 2014. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 50 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
50citing papers in PubMed, 1 pooled it
7.0field-weighted citation impact, top 3% 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

50 citing papers in PubMed, 1 synthesis or guideline pooled it, 118 citations in OpenAlex.

  1. Fourth-generation quinolones in the treatment ofWorld journal of gastroenterology · 2018
    Pooled it
  2. Review
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  4. Review
  5. Review
  6. Article
  7. Review
  8. Microbiology (Reading, England) · 2025
    Article
  9. Therapeutic advances and future directions inFrontiers in microbiology · 2025
    Review
  10. Review
  11. Article
  12. Article
  13. Linolenic acid-metronidazole inhibits the growth ofWorld journal of gastroenterology · 2023
    Article
  14. Bacterial-Mediated Tumor Therapy: Old Treatment in a New Context.Advanced science (Weinheim, Baden-Wurttemberg, Germany) · 2023
    Review
  15. Review
  16. Article
  17. Article
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4 · The record

Corrections and comments

5 · Who and what money

Authors and funding

4 authors at 2 institutions in 1 country.

Soracha ThamphiwatanaDepartment of NanoEngineering, Moores Cancer Center, and.
Weiwei GaoDepartment of NanoEngineering, Moores Cancer Center, and.
Marygorret ObonyoMoores Cancer Center, and Department of Medicine, University of California, San Diego, La Jolla, CA 92093 zhang@ucsd.edu mobonyo@ucsd.edu.
Liangfang ZhangDepartment of NanoEngineering, Moores Cancer Center, and zhang@ucsd.edu mobonyo@ucsd.edu.
Moores Cancer CenterUniversity of California, San Diego · US

Funding

VIRAL MALIGNANCYP30CA023100 · NCI · UNIVERSITY OF CALIFORNIA, SAN DIEGO · PI DIANE M SIMEONE · 1985 to 2026
$124.9M
Innate Antimicrobial Nanotherapeutics for the Treatment of H. pylori InfectionR01DK095168 · NIDDK · UNIVERSITY OF CALIFORNIA, SAN DIEGO · PI ZHANG, LIANGFANG · 2012 to 2016
$1.6M
NCI NIH HHS P30 CA023100NIDDK NIH HHS R01 DK095168NIDDK NIH HHS R01DK095168
6 · The paper itself

Abstract

Helicobacter pylori infection is marked by a vast prevalence and strong association with various gastric diseases, including gastritis, peptic ulcers, and gastric cancer. Because of the rapid emergence of H. pylori strains resistant to existing antibiotics, current treatment regimens show a rapid decline of their eradication rates. Clearly, novel antibacterial strategies against H. pylori are urgently needed. Here, we investigated the in vivo therapeutic potential of liposomal linolenic acid (LipoLLA) for the treatment of H. pylori infection. The LipoLLA formulation with a size of ∼ 100 nm was prone to fusion with bacterial membrane, thereby directly releasing a high dose of linolenic acids into the bacterial membrane. LipoLLA penetrated the mucus layer of mouse stomach, and a significant portion of the administered LipoLLA was retained in the stomach lining up to 24 h after the oral administration. In vivo tests further confirmed that LipoLLA was able to kill H. pylori and reduce bacterial load in the mouse stomach. LipoLLA treatment was also shown to reduce the levels of proinflammatory cytokines including interleukin 1β, interleukin 6, and tumor necrosis factor alpha, which were otherwise elevated because of the H. pylori infection. Finally, a toxicity test demonstrated excellent biocompatibility of LipoLLA to normal mouse stomach. Collectively, results from this study indicate that LipoLLA is a promising, effective, and safe therapeutic agent for the treatment of H. pylori infection.

Indexed as

alpha-Linolenic AcidAnimalsAnti-Bacterial AgentsCarcinomaCell Line, TumorCell MembraneCost-Benefit AnalysisCytokinesDose-Response Relationship, DrugDrug Resistance, BacterialFatty Acids, NonesterifiedGastric MucosaHelicobacter InfectionsHelicobacter pyloriInflammationLiposomesalpha-Linolenic AcidAnti-Bacterial AgentsCytokinesFatty Acids, NonesterifiedLiposomesbacterial infectiondrug deliveryfree fatty acidnanomedicinenanotherapeutics

Identifiers

PMID25422427
PMCPMC4267350
OpenAlexW2008561834

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.