Evidence map›Paper›PMID 23369825›Full record

ReviewTranslational research : the journal of laboratory and clinical medicine2013

Arthritis gene therapy and its tortuous path into the clinic.

Christopher H Evans, Steven C Ghivizzani, Paul D Robbins

Open access · greenAbstract readReview
In one paragraph

Review in Translational research : the journal of laboratory and clinical medicine, 2013. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 30 papers.

0numbers the graph read from it
0cells of the map it votes in
30citing papers in PubMed
9.3field-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

30 citing papers in PubMed, 78 citations in OpenAlex.

  1. Review
  2. Review
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  18. Anatomically shaped tissue-engineered cartilage with tunable and inducible anticytokine delivery for biological joint resurfacing.Proceedings of the National Academy of Sciences of the United States of America · 2016
    Article
  19. Article
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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

3 authors at 3 institutions in 1 country.

Christopher H EvansDepartment of Orthopedic Surgery, Harvard Medical School, Boston, Mass., USA. cevans@bidmc.harvard.edu
Steven C Ghivizzani
Paul D Robbins
Harvard University · USScripps Research Institute · USUniversity of Florida · US

Funding

Utility of AAV Serotypes for Gene Delivery in Treatment of Chronic Joint DiseaseR01AR048566 · NIAMS · UNIVERSITY OF FLORIDA · PI GHIVIZZANI, STEVEN C · 2003 to 2013
$3.6M
Transfer of IL-1Ra cDNA to the Human, Osteoarthritic KneeR01AR051085 · NIAMS · BRIGHAM AND WOMEN'S HOSPITAL · PI EVANS, CHRISTOPHER HOWARD · 2005 to 2008
$1.6M
Delivery of Soluble FGFR3 as a Treatment for AchondroplasiaR01AR057422 · NIAMS · UNIVERSITY OF FLORIDA · PI GHIVIZZANI, STEVEN C · 2010 to 2014
$1.6M
Delivery of Therapeutic Genes to Osteoarthritic JointsR21AR049606 · NIAMS · BRIGHAM AND WOMEN'S HOSPITAL · PI EVANS, CHRISTOPHER H · 2002 to 2002
$173k
CLINICAL TRIAL OF GENE THERAPY FOR ARTHRITISR01AR043623 · NIAMS · UNIVERSITY OF PITTSBURGH AT PITTSBURGH · PI EVANS, CHRISTOPHER H · 1996 to 1998
–
NIAMS NIH HHS R01 AR048566NIAMS NIH HHS R01 AR051085NIAMS NIH HHS R01 AR057422NIAMS NIH HHS R01 AR43623NIAMS NIH HHS R21 AR049606NINDS NIH HHS X01 NS066865
6 · The paper itself

Abstract

Arthritis is a disease of joints. The biology of joints makes them very difficult targets for drug delivery in a manner that is specific and selective. This is especially true for proteinaceous drugs ("biologics"). Gene transfer is the only technology that can solve the delivery problem in a clinically reasonable fashion. There is an abundance of preclinical data confirming that genes can be efficiently transferred to tissues within joints by intra-articular injection using a variety of different vectors in conjunction with ex vivo and in vivo strategies. Using the appropriate gene transfer technologies, long-term, intra-articular expression of anti-arthritic transgenes at therapeutic concentrations can be achieved. Numerous studies confirm that gene therapy is effective in treating experimental models of rheumatoid arthritis (RA) and osteoarthritis (OA) in the laboratory. A limited number of clinical trials have been completed, which confirm safety and feasibility but only 3 protocols have reached phase II; as yet, there is no unambiguous evidence of efficacy in human disease. Only 2 clinical trials are presently underway, both phase II studies using allogeneic chondrocytes expressing transforming growth factor-β1 for the treatment of OA. Phase I studies using adeno-associated virus to deliver interleukin-1Ra in OA and interferon-β in RA are going through the regulatory process. It is to be hoped that the recent successes in treating rare, Mendelian diseases by gene therapy will lead to accelerated development of genetic treatments for common, non-Mendelian diseases, such as arthritis.

Indexed as

Genetic TherapyTranslational Research, BiomedicalAnimalsArthritisClinical Trials as TopicGene Transfer TechniquesHumansJoints

Identifiers

PMID23369825
PMCPMC3602127
OpenAlexW2063795648

What OpenQuestion holds

Textmetadata
LicenceTDM
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.