Evidence map›Paper›PMID 27413147›Full record

ArticleThe Journal of neuroscience : the official journal of the Society for Neuroscience2016

IL4-10 Fusion Protein Is a Novel Drug to Treat Persistent Inflammatory Pain.

Niels Eijkelkamp, Cristine Steen-Louws, Sarita A Y Hartgring, Hanneke L D M Willemen, Judith Prado, Floris P J G Lafeber, Cobi J Heijnen, C E Hack, Joel A G van Roon, Annemieke Kavelaars

Open access · bronzeAbstract read
In one paragraph

Article in The Journal of neuroscience : the official journal of the Society for Neuroscience, 2016. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 52 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
52citing papers in PubMed, 1 pooled it
5.6field-weighted citation impact, top 4% 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

52 citing papers in PubMed, 1 synthesis or guideline pooled it, 76 citations in OpenAlex.

  1. Pooled it
  2. Glial cells in neuropathic pain.Physiological reviews · 2026
    Review
  3. Article
  4. Review
  5. Article
  6. Article
  7. Article
  8. Article
  9. Review
  10. Article
  11. Article
  12. Article
  13. Evolving techniques for reducing phantom limb pain.Experimental biology and medicine (Maywood, N.J.) · 2023
    Review
  14. Review
  15. Article
  16. Article
  17. Article
  18. Review
  19. Article
  20. Article
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

10 authors at 3 institutions in 4 countries.

Niels EijkelkampLaboratories of Translational Immunology and Neuroimmunology and Developmental Origins of Disease and n.eijkelkamp@umcutrecht.nl.ORCID 0000-0003-0039-7063
Cristine Steen-LouwsLaboratories of Translational Immunology and.
Sarita A Y HartgringLaboratories of Translational Immunology and.
Hanneke L D M WillemenNeuroimmunology and Developmental Origins of Disease and.
Judith PradoLaboratories of Translational Immunology and.
Floris P J G LafeberDepartment of Rheumatology and Clinical Immunology, University Medical Center Utrecht, 3584 EA Utrecht, The Netherlands, and.
Cobi J HeijnenNeuroimmunology Laboratory, Department of Symptom Research, MD Anderson Cancer Center, University of Texas, Houston, Texas 77030.ORCID 0000-0002-1928-3050
C E HackLaboratories of Translational Immunology and.
Joel A G van RoonLaboratories of Translational Immunology and.
Annemieke KavelaarsNeuroimmunology Laboratory, Department of Symptom Research, MD Anderson Cancer Center, University of Texas, Houston, Texas 77030.
International Society for Developmental Origins of Health and Disease · GBThe University of Texas MD Anderson Cancer Center · USUniversity Medical Center Utrecht · NL

Funding

Neuroimmune Mechanisms of Recovery from Comorbid Depression and Chronic PainR01NS073939 · NINDS · UNIVERSITY OF TX MD ANDERSON CAN CTR · PI DANTZER, ROBERT, HEIJNEN, COBI J · 2011 to 2020
$4.0M
A novel molecular switch regulating transition from acute to chronic pain.R01NS074999 · NINDS · UNIVERSITY OF TX MD ANDERSON CAN CTR · PI KAVELAARS, ANNEMIEKE · 2011 to 2015
$1.7M
NINDS NIH HHS R01 NS073939NINDS NIH HHS R01 NS074999
6 · The paper itself

Abstract

unlabelledChronic pain is a major clinical problem that is difficult to treat and requires novel therapies. Although most pain therapies primarily target neurons, neuroinflammatory processes characterized by spinal cord and dorsal root ganglion production of proinflammatory cytokines play an important role in persistent pain states and represent potential therapeutic targets. Anti-inflammatory cytokines are attractive candidates to regulate aberrant neuroinflammatory processes, but the therapeutic potential of these cytokines as stand-alone drugs is limited. Their optimal function requires concerted actions with other regulatory cytokines, and their relatively small size causes rapid clearance. To overcome these limitations, we developed a fusion protein of the anti-inflammatory cytokines interleukin 4 (IL4) and IL10. The IL4-10 fusion protein is a 70 kDa glycosylated dimeric protein that retains the functional activity of both cytokine moieties. Intrathecal administration of IL4-10 dose-dependently inhibited persistent inflammatory pain in mice: three IL4-10 injections induced full resolution of inflammatory pain in two different mouse models of persistent inflammatory pain. Both cytokine moieties were required for optimal effects. The IL4-10 fusion protein was more effective than the individual cytokines or IL4 plus IL10 combination therapy and also inhibited allodynia in a mouse model of neuropathic pain. Mechanistically, IL4-10 inhibited the activity of glial cells and reduced spinal cord and dorsal root ganglion cytokine levels without affecting paw inflammation. In conclusion, we developed a novel fusion protein with improved efficacy to treat pain, compared with wild-type anti-inflammatory cytokines. The IL4-10 fusion protein has potential as a treatment for persistent inflammatory pain. SIGNIFICANCE STATEMENT: The treatment of chronic pain is a major clinical and societal challenge. Current therapies to treat persistent pain states are limited and often cause major side effects. Therefore, novel analgesic treatments are urgently needed. In search of a novel drug to treat chronic pain, we developed a fusion protein consisting of two prototypic regulatory cytokines, interleukin 4 (IL4) and IL10. The work presented in this manuscript shows that this IL4-10 fusion protein overcomes some major therapeutic limitations of pain treatment with individual cytokines. The IL4-10 fusion protein induces full resolution of persistent inflammatory pain in two different mouse models. These novel findings are significant, as they highlight the IL4-10 fusion protein as a long-needed potential new drug to stop persistent pain states.

Indexed as

AnalgesicsAnimalsCarrageenanCells, CulturedDisease Models, AnimalFemaleFreund's AdjuvantHumansInflammationInterleukin-10Interleukin-4LipopolysaccharidesMaleMiceMice, Inbred C57BLNeuralgiaAnalgesicsCarrageenanFreund's AdjuvantIL10 protein, humanIL4 protein, humanInterleukin-10Interleukin-4LipopolysaccharidesRecombinant Fusion Proteinsanti-inflammatory cytokinesfusion proteingliainflammatory pain

Identifiers

PMID27413147
PMCPMC4945660
OpenAlexW2466485063

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.