Evidence map›Paper›PMID 23333631›Full record

ArticleArchives of biochemistry and biophysics2013

Transport of anti-IL-6 antigen binding fragments into cartilage and the effects of injury.

Sangwon Byun, Yunna L Sinskey, Yihong C S Lu, Tatiana Ort, Karl Kavalkovich, Pitchumani Sivakumar, Ernst B Hunziker, Eliot H Frank, Alan J Grodzinsky

Open access · bronzeAbstract read
In one paragraph

Article in Archives of biochemistry and biophysics, 2013. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 16 papers.

0numbers the graph read from it
0cells of the map it votes in
16citing papers in PubMed
2.3field-weighted citation impact, top 13% 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

16 citing papers in PubMed, 24 citations in OpenAlex.

  1. Review
  2. Article
  3. Article
  4. Article
  5. Review
  6. WNT3A-loaded exosomes enable cartilage repair.Journal of extracellular vesicles · 2021
    Article
  7. Targeting Cartilage Degradation in Osteoarthritis.Pharmaceuticals (Basel, Switzerland) · 2021
    Review
  8. Article
  9. Review
  10. Review
  11. Nitric oxide-associated chondrocyte apoptosis in trauma patients after high-energy lower extremity intra-articular fractures.Journal of orthopaedics and traumatology : official journal of the Italian Society of Orthopaedics and Traumatology · 2015
    Article
  12. Review
  13. Article
  14. Article
  15. Article
  16. 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

9 authors at 3 institutions in 2 countries.

Sangwon ByunDepartment of Electrical Engineering and Computer Science, Massachusetts Institute of Technology, Cambridge, MA 02139, United States.
Yunna L Sinskey
Yihong C S Lu
Tatiana Ort
Karl Kavalkovich
Pitchumani Sivakumar
Ernst B Hunziker
Eliot H Frank
Alan J Grodzinsky
Massachusetts Institute of Technology · USJanssen (United States) · USUniversity of Bern · CH

Funding

MECHANISMS OF CHONDROCYTE RESPONSE TO MECHANICAL STIMULIR01AR045779 · NIAMS · MASSACHUSETTS INSTITUTE OF TECHNOLOGY · PI GRODZINSKY, ALAN J. · 1998 to 2008
$2.1M
Cartilage Repair Using Self Assembling Peptide ScaffoldsR01AR060331 · NIAMS · MASSACHUSETTS INSTITUTE OF TECHNOLOGY · PI GRODZINSKY, ALAN J. · 2012 to 2016
$1.7M
NIAMS NIH HHS AR45779NIAMS NIH HHS AR60331NIAMS NIH HHS R01 AR045779NIAMS NIH HHS R01 AR060331
6 · The paper itself

Abstract

The efficacy of biological therapeutics against cartilage degradation in osteoarthritis is restricted by the limited transport of macromolecules through the dense, avascular extracellular matrix. The availability of biologics to cell surface and matrix targets is limited by steric hindrance of the matrix, and the microstructure of matrix itself can be dramatically altered by joint injury and the subsequent inflammatory response. We studied the transport into cartilage of a 48 kDa anti-IL-6 antigen binding fragment (Fab) using an in vitro model of joint injury to quantify the transport of Fab fragments into normal and mechanically injured cartilage. The anti-IL-6 Fab was able to diffuse throughout the depth of the tissue, suggesting that Fab fragments can have the desired property of achieving local delivery to targets within cartilage, unlike full-sized antibodies which are too large to penetrate beyond the cartilage surface. Uptake of the anti-IL-6 Fab was significantly increased following mechanical injury, and an additional increase in uptake was observed in response to combined treatment with TNFα and mechanical injury, a model used to mimic the inflammatory response following joint injury. These results suggest that joint trauma leading to cartilage degradation can further alter the transport of such therapeutics and similar-sized macromolecules.

Indexed as

AdultAnimalsCartilage, ArticularCattleFemaleHumansImmunoglobulin Fab FragmentsInterleukin-6Protein TransportStress, MechanicalTumor Necrosis Factor-alphaImmunoglobulin Fab FragmentsInterleukin-6Tumor Necrosis Factor-alpha

Identifiers

PMID23333631
PMCPMC3596461
OpenAlexW2055772296

What OpenQuestion holds

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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.