Evidence map›Paper›PMID 28275260›Full record

ReviewNature reviews. Rheumatology2017

Beyond TNF: TNF superfamily cytokines as targets for the treatment of rheumatic diseases.

Michael Croft, Richard M Siegel

Open access · greenAbstract readReview
In one paragraph

Review in Nature reviews. Rheumatology, 2017. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 155 papers.

0numbers the graph read from it
0cells of the map it votes in
155citing papers in PubMed
24.5field-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

155 citing papers in PubMed, 282 citations in OpenAlex.

  1. Article
  2. Review
  3. Review
  4. Pathogenic role of MIF receptor (CD74) expressing T cells in inflammatory arthritis.Proceedings of the National Academy of Sciences of the United States of America · 2026
    Article
  5. Article
  6. Article
  7. Article
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  9. Combined TNF-α and OX40L targeting as a new treatment option for hidradenitis suppurativa.The journal of allergy and clinical immunology. Global · 2025
    Article
  10. Review
  11. Article
  12. Article
  13. Article
  14. Article
  15. Article
  16. Article
  17. Article
  18. Review
  19. Review
  20. Article

95 more citing papers are in PubMed but not listed here.

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

2 authors at 2 institutions in 1 country.

Michael CroftDivision of Immune Regulation, La Jolla Institute for Allergy and Immunology, and Department of Medicine, University of California San Diego, La Jolla, California 92037, USA.
Richard M SiegelImmunoregulation Section, Autoimmunity Branch, NIAMS, NIH, Bethesda, Maryland, USA.
National Institute of Arthritis and Musculoskeletal and Skin Diseases · USUniversity of California, San Diego · US

Funding

TRM and airway inflammation and remodelingU19AI070535 · NIAID · UNIVERSITY OF CALIFORNIA, SAN DIEGO · PI BROIDE, DAVID H · 2006 to 2025
$34.2M
TNF-receptors and programmed cell death in regulation of autoimmunityZIAAR041133 · NIAMS · NATIONAL INSTITUTE OF ARTHRITIS AND MUSCULOSKELETAL AND SKIN DISEASES · PI SIEGEL, RICHARD M · 2009 to 2019
$9.3M
Control of Airway ToleranceR01AI103021 · NIAID · LA JOLLA INSTITUTE FOR IMMUNOLOGY · PI CROFT, MICHAEL · 2013 to 2017
$2.2M
Novel PTPRD interaction Controlling T cell ResponsivenessR21AI123134 · NIAID · LA JOLLA INSTITUTE FOR IMMUNOLOGY · PI CROFT, MICHAEL · 2016 to 2017
$487k
Structural Characterization of 4-1BB-Galectin-9 ComplexesR03AI110929 · NIAID · LA JOLLA INSTITUTE FOR IMMUNOLOGY · PI CROFT, MICHAEL, ZAJONC, DIRK M · 2014 to 2015
$177k
NIAID NIH HHS R01 AI103021NIAID NIH HHS R03 AI110929NIAID NIH HHS R21 AI123134NIAID NIH HHS U19 AI070535
6 · The paper itself

Abstract

TNF blockers are highly efficacious at dampening inflammation and reducing symptoms in rheumatic diseases such as rheumatoid arthritis, psoriatic arthritis and ankylosing spondylitis, and also in nonrheumatic syndromes such as inflammatory bowel disease. As TNF belongs to a superfamily of 19 structurally related proteins that have both proinflammatory and anti-inflammatory activity, reagents that disrupt the interaction between proinflammatory TNF family cytokines and their receptors, or agonize the anti-inflammatory receptors, are being considered for the treatment of rheumatic diseases. Biologic agents that block B cell activating factor (BAFF) and receptor activator of nuclear factor-κB ligand (RANKL) have been approved for the treatment of systemic lupus erythematosus and osteoporosis, respectively. In this Review, we focus on additional members of the TNF superfamily that could be relevant for the pathogenesis of rheumatic disease, including those that can strongly promote activity of immune cells or increase activity of tissue cells, as well as those that promote death pathways and might limit inflammation. We examine preclinical mouse and human data linking these molecules to the control of damage in the joints, muscle, bone or other tissues, and discuss their potential as targets for future therapy of rheumatic diseases.

Indexed as

Molecular Targeted TherapyTumor Necrosis Factor Inhibitors4-1BB LigandAnimalsCD27 LigandCD40 LigandCell DeathCytokine TWEAKDendritic CellsFas Ligand ProteinHumansImmune ToleranceLymphocyte ActivationLymphotoxin-alphaOX40 LigandRheumatic Diseases4-1BB LigandCD27 LigandCD40 LigandCytokine TWEAKFas Ligand ProteinLymphotoxin-alphaOX40 LigandTNF-Related Apoptosis-Inducing LigandTNFSF12 protein, humanTNFSF18 protein, humanTumor Necrosis Factor InhibitorsTumor Necrosis Factor Ligand Superfamily Member 14Tumor Necrosis Factor Ligand Superfamily Member 15Tumor Necrosis Factors

Identifiers

PMID28275260
PMCPMC5486401
OpenAlexW2592820806

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.