Evidence map›Paper›PMID 32609496›Full record

ArticleBioconjugate chemistry2020

Localization of Therapeutic Fab-CHP Conjugates to Sites of Denatured Collagen for the Treatment of Rheumatoid Arthritis.

Keith J Arlotta, Boi Hoa San, Hong-Hua Mu, S Michael Yu, Shawn C Owen

Open access · greenAbstract read
In one paragraph

Article in Bioconjugate chemistry, 2020. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 12 papers.

0numbers the graph read from it
0cells of the map it votes in
12citing papers in PubMed
0.6field-weighted citation impact, top 30% 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

12 citing papers in PubMed, 13 citations in OpenAlex.

  1. Article
  2. Article
  3. Article
  4. Article
  5. Collagen Hybridizing Peptide-Based Radiotracers for Molecular Imaging of Collagen Turnover in Pulmonary Fibrosis.Journal of nuclear medicine : official publication, Society of Nuclear Medicine · 2025
    Article
  6. Article
  7. Article
  8. Article
  9. Targeting damaged collagen for intra-articular delivery of therapeutics using collagen hybridizing peptides.Journal of orthopaedic research : official publication of the Orthopaedic Research Society · 2023
    Article
  10. The Chemistry and Biology of Collagen Hybridization.Journal of the American Chemical Society · 2023
    Review
  11. Collagen Molecular Damage is a Hallmark of Early Atherosclerosis Development.Journal of cardiovascular translational research · 2023
    Article
  12. 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

5 authors at 1 institution in 1 country.

Keith J ArlottaDepartment of Biomedical Engineering, University of Utah, Salt Lake City, Utah 84112, United States.
Boi Hoa SanDepartment of Biomedical Engineering, University of Utah, Salt Lake City, Utah 84112, United States.ORCID 0000-0001-5340-4920
Hong-Hua MuDepartment of Internal Medicine, University of Utah, Salt Lake City, Utah 84132, United States.
S Michael YuDepartment of Biomedical Engineering, University of Utah, Salt Lake City, Utah 84112, United States.ORCID 0000-0002-5171-2644
Shawn C OwenDepartment of Biomedical Engineering, University of Utah, Salt Lake City, Utah 84112, United States.ORCID 0000-0001-5996-7679
University of Utah · US

Funding

Sustained Intravitreal Delivery of Ranibizumab Mediated by ECM BindingR21EY029430 · NEI · UNIVERSITY OF UTAH · PI YU, MICHAEL S · 2018 to 2019
$419k
NEI NIH HHS R21 EY029430
6 · The paper itself

Abstract

Rheumatoid arthritis (RA) is an autoimmune disease characterized by chronic inflammation in synovial joints and protease-induced cartilage degradation. Current biologic treatments for RA can effectively reduce symptoms, primarily by neutralizing the proinflammatory cytokine TNFα; however, continued, indiscriminate overinhibition of inflammatory factors can significantly weaken the host immune system, leading to opportunistic infections and interrupting treatment. We hypothesize that localizing anti-TNFα therapeutics to denatured collagen (dCol) present at arthritic joints, via conjugation with collagen-hybridizing peptides (CHPs), will reduce off-site antigen binding and maintain local immunosuppression. We isolated the antigen-binding fragment of the clinically approved anti-TNFα therapeutic infliximab (iFab) and prepared iFab-CHP conjugates via lysine-based conjugation with an SMCC linker. After successful conjugation, confirmed by LC-MS, the binding affinity of iFab-CHP was characterized by ELISA-like assays, which showed comparable antigen binding relative to infliximab, comparable dCol binding relative to CHP, and the hybrid ability to bind both dCol and TNFα simultaneously. We further demonstrated localization of Fab-CHP to areas of high dCol in vivo and promising therapeutic efficacy, assessed by histological staining (Safranin-O and H&E), in a pilot mouse study.

Indexed as

AnimalsAntibodiesAntigensAntirheumatic AgentsChromatography, LiquidCollagenFemaleImmunoglobulin Fab FragmentsInfliximabMass SpectrometryMiceMice, NudeMice, TransgenicPeptidesProtein BindingTumor Necrosis Factor-alphaAntibodiesAntigensAntirheumatic AgentsCollagenImmunoglobulin Fab FragmentsInfliximabPeptidesTumor Necrosis Factor-alpha

Identifiers

PMID32609496
PMCPMC9682596
OpenAlexW3038290948

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.