Evidence map›Paper›PMID 26579954›Full record

ArticleNucleic acid therapeutics2016

Chemically Modified Interleukin-6 Aptamer Inhibits Development of Collagen-Induced Arthritis in Cynomolgus Monkeys.

Masao Hirota, Ikuo Murakami, Yuichi Ishikawa, Tomoki Suzuki, Shun-ichiro Sumida, Shigeru Ibaragi, Hayato Kasai, Naoto Horai, Daniel W Drolet, Shashi Gupta and 2 more

Open access · hybridAbstract read
In one paragraph

Article in Nucleic acid therapeutics, 2016. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 23 papers.

0numbers the graph read from it
0cells of the map it votes in
23citing papers in PubMed
3.2field-weighted citation impact, top 8% 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

23 citing papers in PubMed, 38 citations in OpenAlex.

  1. Article
  2. Review
  3. Review
  4. Recent Advances of Trained immunity in Macrophages.International journal of biological sciences · 2025
    Review
  5. Article
  6. Article
  7. Generation of Specific Aptamers.Methods in molecular biology (Clifton, N.J.) · 2024
    Article
  8. Review
  9. Article
  10. Review
  11. Review
  12. Article
  13. Article
  14. Article
  15. Review
  16. Article
  17. Article
  18. Article
  19. Future strategies for the discovery of therapeutic aptamers.Expert opinion on drug discovery · 2017
    Article
  20. 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

12 authors at 3 institutions in 2 countries.

Masao Hirota1 Otsuka Pharmaceutical Co., Ltd. , Tokushima, Japan .
Ikuo Murakami1 Otsuka Pharmaceutical Co., Ltd. , Tokushima, Japan .
Yuichi Ishikawa1 Otsuka Pharmaceutical Co., Ltd. , Tokushima, Japan .
Tomoki Suzuki1 Otsuka Pharmaceutical Co., Ltd. , Tokushima, Japan .
Shun-ichiro Sumida1 Otsuka Pharmaceutical Co., Ltd. , Tokushima, Japan .
Shigeru Ibaragi1 Otsuka Pharmaceutical Co., Ltd. , Tokushima, Japan .
Hayato Kasai2 Shin Nippon Biomedical Laboratories, Ltd. , Drug Safety Research Laboratories, Kagoshima, Japan .
Naoto Horai2 Shin Nippon Biomedical Laboratories, Ltd. , Drug Safety Research Laboratories, Kagoshima, Japan .
Daniel W Drolet3 SomaLogic, Inc. , Boulder, Colorado.
Shashi Gupta3 SomaLogic, Inc. , Boulder, Colorado.
Nebojsa Janjic3 SomaLogic, Inc. , Boulder, Colorado.
Daniel J Schneider3 SomaLogic, Inc. , Boulder, Colorado.
Otsuka (Japan) · JPSomaLogic (United States) · USShin Nippon Biomedical Laboratories (Japan) · JP

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Interleukin-6 (IL-6) is a potent mediator of inflammatory and immune responses, and a validated target for therapeutic intervention of inflammatory diseases. Previous studies have shown that SL1026, a slow off-rate modified aptamer (SOMAmer) antagonist of IL-6, neutralizes IL-6 signaling in vitro. In the present study, we show that SL1026 delays the onset and reduces the severity of rheumatoid symptoms in a collagen-induced arthritis model in cynomolgus monkeys. SL1026 (1 and 10 mg/kg), administered q.i.d., delayed the progression of arthritis and the concomitant increase in serum IL-6 levels compared to the untreated control group. Furthermore, SL1026 inhibited IL-6-induced STAT3 phosphorylation ex vivo in T lymphocytes from human blood and IL-6-induced C-reactive protein and serum amyloid A production in human primary hepatocytes. Importantly, SOMAmer treatment did not elicit an immune response, as evidenced by the absence of anti-SOMAmer antibodies in plasma of treated monkeys. These results demonstrate that SOMAmer antagonists of IL-6 may be attractive agents for the treatment of IL-6-mediated diseases, including rheumatoid arthritis.

Indexed as

Amino Acid SequenceAnimalsAptamers, PeptideArthritis, ExperimentalCells, CulturedCollagenFemaleHumansInterleukin-6Macaca fascicularisMolecular Sequence DataPhosphorylationSequence Homology, Amino AcidSTAT3 Transcription FactorT-LymphocytesAptamers, PeptideCollagenInterleukin-6STAT3 Transcription Factor

Identifiers

PMID26579954
PMCPMC4753578
OpenAlexW2400223198

What OpenQuestion holds

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LicenceCC BY
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Registered trials

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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.