Evidence map›Paper›PMID 31140325›Full record

ArticleHuman gene therapy2019

Lentiviral CRISPR Epigenome Editing of Inflammatory Receptors as a Gene Therapy Strategy for Disc Degeneration.

Niloofar Farhang, Matt Ginley-Hidinger, Kristofer C Berrett, Jason Gertz, Brandon Lawrence, Robby D Bowles

Open access · greenAbstract read
In one paragraph

Article in Human gene therapy, 2019. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 34 papers.

0numbers the graph read from it
0cells of the map it votes in
34citing papers in PubMed
15.9field-weighted citation impact, top 1% 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

34 citing papers in PubMed, 67 citations in OpenAlex.

  1. Article
  2. Article
  3. Article
  4. Review
  5. Intervertebral disc degeneration.Nature reviews. Disease primers · 2026
    Review
  6. Regenerative strategies for intervertebral disc degeneration.Journal of orthopaedic translation · 2025
    Review
  7. Article
  8. Review
  9. Article
  10. Harnessing CRISPR potential for intervertebral disc regeneration strategies.Frontiers in bioengineering and biotechnology · 2025
    Review
  11. Article
  12. Therapeutic CRISPR epigenome editing of inflammatory receptors in the intervertebral disc.Molecular therapy : the journal of the American Society of Gene Therapy · 2024
    Article
  13. Article
  14. Review
  15. CRISPR/Cas9 systems: Delivery technologies and biomedical applications.Asian journal of pharmaceutical sciences · 2023
    Review
  16. Article
  17. Review
  18. Article
  19. 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

6 authors at 1 institution in 1 country.

Niloofar FarhangDepartment of Biomedical Engineering, University of Utah, Salt Lake City, Utah.
Matt Ginley-HidingerDepartment of Biomedical Engineering, University of Utah, Salt Lake City, Utah.
Kristofer C BerrettDepartment of Oncological Sciences, University of Utah, Salt Lake City, Utah.
Jason GertzDepartment of Oncological Sciences, University of Utah, Salt Lake City, Utah.
Brandon LawrenceDepartment of Orthopaedics, University of Utah, Salt Lake City, Utah.
Robby D BowlesDepartment of Biomedical Engineering, University of Utah, Salt Lake City, Utah.
University of Utah · US

Funding

Sequence-specific CRISPR mediated inflammatory cytokine receptor modulation for the treatment of inflammatory intervertebral disc pathologyR01AR074998 · NIAMS · UNIVERSITY OF UTAH · PI BOWLES, ROBERT D. · 2019 to 2023
$1.7M
Univ of Utah Cell Sorter for Flow Cytometry CoreS10RR026802 · NCRR · UNIVERSITY OF UTAH · PI GREEN, WAYNE FRANCIS · 2010 to 2010
$500k
Sequence-Specific CRISPR Mediated Inflammatory Cytokine Receptor Modulation for the Treatment of Inflammatory Intervertebral Disc PathologyR03AR068777 · NIAMS · UNIVERSITY OF UTAH · PI BOWLES, ROBERT D. · 2015 to 2017
$224k
NCRR NIH HHS S10 RR026802NIAMS NIH HHS R01 AR074998NIAMS NIH HHS R03 AR068777
6 · The paper itself

Abstract

Degenerative disc disease (DDD) is a primary contributor to low-back pain, a leading cause of disability. Progression of DDD is aided by inflammatory cytokines in the intervertebral disc (IVD), particularly TNF-α and IL-1β, but current treatments fail to effectively target this mechanism. The objective of this study was to explore the feasibility of Clustered Regularly Interspaced Short Palindromic Repeats (CRISPR) epigenome editing-based therapy for DDD, by modulation of TNFR1/IL1R1 signaling in pathological human IVD cells. Human IVD cells from the nucleus pulposus of patients receiving surgery for back pain were obtained and the regulation of TNFR1/IL1R1 signaling by a lentiviral CRISPR epigenome editing system was tested. These cells were tested for successful lentiviral transduction/expression of deactivated Cas9 fused to Krüppel Associated Box system and regulation of TNFR1/IL1R1 expression. TNFR1/IL1R1 signaling disruption was investigated through measurement of NF-κB activity, apoptosis, and anabolic/catabolic changes in gene expression postinflammatory challenge. CRISPR epigenome editing systems were effectively introduced into pathological human IVD cells and significantly downregulated TNFR1 and IL1R1. This downregulation significantly attenuated deleterious TNFR1 signaling but not IL1R1 signaling. This is attributed to less robust IL1R1 expression downregulation, and IL-1β-driven reversal of IL1R1 expression downregulation in a portion of patient IVD cells. In addition, RNAseq data indicated novel transcription factor targets, IRF1 and TFAP2C, as being primary regulators of inflammatory signaling in IVD cells. These results demonstrate the feasibility of CRISPR epigenome editing of inflammatory receptors in pathological IVD cells, but highlight a limitation in epigenome targeting of IL1R1. This method has potential application as a novel gene therapy for DDD, to attenuate the deleterious effect of inflammatory cytokines present in the degenerative IVD.

Indexed as

Clustered Regularly Interspaced Short Palindromic RepeatsEpigenesis, GeneticGene EditingGenetic TherapyApoptosisBiomarkersCells, CulturedGene Expression RegulationGene OrderGenetic VectorsGene Transfer TechniquesHumansIntervertebral Disc DegenerationLentivirusReceptors, ImmunologicReceptors, Interleukin-1 Type IBiomarkersIL1R1 protein, humanReceptors, ImmunologicReceptors, Interleukin-1 Type IReceptors, Tumor Necrosis Factor, Type ICRISPRdegenerative disc diseaseepigenome editinggene therapyinflammationreceptor

Identifiers

PMID31140325
PMCPMC6761595
OpenAlexW2947265019

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.