Evidence map›Paper›PMID 30610229›Full record

ArticleEye (London, England)2019

Interruption of autoimmunity for thyroid eye disease: B-cell and T-cell strategy.

Diego Strianese, Francesca Rossi

Open access · bronzeAbstract readConference Proceedings
In one paragraph

Article in Eye (London, England), 2019. 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
2.9field-weighted citation impact, top 9% 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, 30 citations in OpenAlex.

  1. Article
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  3. Review
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  5. Article
  6. Article
  7. Systemic diseases and the cornea.Experimental eye research · 2021
    Review
  8. Review
  9. Article
  10. Review
  11. Article
  12. Article
  13. Review
  14. Monoclonal antibodies for the treatment of Graves' ophthalmopathy: A systematic review and meta-analysis.Saudi journal of ophthalmology : official journal of the Saudi Ophthalmological Society
    Article
  15. Review
  16. 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

2 authors at 2 institutions in 2 countries.

Diego StrianeseDepartment of Neuroscience, University of Naples -Federico II, Naples, Italy and, - Orbital Unit-King Khaled Eye Specialist Hospital, Riyadh, Saudi Arabia. dstrianese@kkesh.med.sa.
Francesca RossiDepartment of Translational Medical Sciences and Center for Basic and Clinical Immunology Research, University of Naples Federico II, Naples, Italy.
King Khaled Eye Specialist Hospital · SAUniversity of Naples Federico II · IT

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Recent new insights into the molecular basis of thyroid eye disease have led to the use of more specific therapies such as monoclonal antibodies This review explores the traditional immunosuppressant therapy for TED, highlighting the basis for emergent recent medications, possible treatment options and, eventually possible new general recommendation for management of TED. Data has been retrieved from the literature searching on Pubmed. Steroid therapy remains the first line therapy for moderate/severe and severe vision threatening TED The use of some traditional nonspecific immunosuppressant such as mycophenolate, cyclosporine and azathioprine seems useful in combination with steroid therapy to achieve stable results in the long term; methotrexate is useful as steroid-sparing medications and in steroid resistant or intolerant patients. In recent years, many scientific reports have showed the effectiveness of biological immunosuppressive agents in the management of TED. Etanercept, adalimumab, and tocilizumab have shown to be effective in reduction of the inflammatory signs with the possible advantage to prevent relapse of the disease. Particularly Tociliuzumab seems very effective as second line therapy, after steroid failure. Teprotumumab may control the disease activity and it seems to be very effective in preventing severity disease progression. Infliximab might be useful in severe TED with optic nerve compression resistant to steroid and decompression. Indeed, the actual incidence of adverse effects is not well assessed yet, therefore the use should be limited at those cases that really need an alternative therapy to steroid, handled by an expert multidisciplinary team.

Indexed as

Antibodies, MonoclonalAntibodies, Monoclonal, HumanizedAutoimmunityB-LymphocytesCongresses as TopicGraves OphthalmopathyHumansImmunosuppressive AgentsReceptor, IGF Type 1Receptors, SomatomedinT-LymphocytesAntibodies, MonoclonalAntibodies, Monoclonal, HumanizedIGF1R protein, humanImmunosuppressive AgentsReceptor, IGF Type 1Receptors, Somatomedinteprotumumab

Identifiers

PMID30610229
PMCPMC6367473
OpenAlexW2906925165

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.