Evidence map›Paper›PMID 28701761›Full record

ReviewNature reviews. Rheumatology2017

Antigen-specific immunotherapies in rheumatic diseases.

Judit Pozsgay, Zoltán Szekanecz, Gabriella Sármay

Abstract readReview
PubMed Publisher
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 47 papers, 3 of them syntheses that pooled it.

0numbers the graph read from it
0cells of the map it votes in
47citing papers in PubMed, 3 pooled it
10.4field-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

47 citing papers in PubMed, 3 syntheses or guidelines pooled it, 82 citations in OpenAlex.

  1. Pooled it
  2. Controlling timing and location in vaccines.Advanced drug delivery reviews · 2020
    Pooled it
  3. Pooled it
  4. Depleting Autoreactive B‑Cells Using Targeted Photodynamic Therapy.ACS pharmacology & translational science · 2025
    Article
  5. Article
  6. Review
  7. Article
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  9. Review
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  12. Impact of Siglecs on autoimmune diseases.Molecular aspects of medicine · 2023
    Review
  13. Review
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  15. Review
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  19. Review
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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 2 institutions in 1 country.

Judit PozsgayDepartment of Immunology, Eötvös Loránd University (ELTE), Pázmány Péter Sétány 1/C, Budapest 1117, Hungary.
Zoltán SzekaneczDivision of Rheumatology, Department of Medicine, University of Debrecen Faculty of Medicine, Nagyerdei Körút 98, Debrecen 4032, Hungary.
Gabriella SármayDepartment of Immunology, Eötvös Loránd University (ELTE), Pázmány Péter Sétány 1/C, Budapest 1117, Hungary.
Eötvös Loránd University · HUUniversity of Debrecen · HU

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

The main goal of antigen-specific immunotherapy (ASI) in autoimmune and rheumatic diseases is to reprogramme or remove autoreactive cells and/or induce immune tolerance to self-antigens. Current therapies in these diseases either treat symptoms or slow down disease progression but are not yet curative or preventative - disease-specific treatments are urgently needed. In contrast to the nonspecific treatments in current use that induce generalized immune suppression, which is associated with several adverse effects including increased risk of infections, ASIs target a restricted subset of B cells or T cells, and thus do not compromise systemic immunity and host defence. This Review provides a summary of novel approaches for identifying autoepitopes and detecting and targeting autoreactive cells that might help in the development of ASIs. Promising approaches include the use of tolerizing peptides coupled to MHC constructs and/or nanocompounds, tolerizing dendritic cells and antigen-specific vaccines. Following studies in animal models of rheumatoid arthritis and systemic lupus erythematosus, several of these strategies have now entered clinical trials. However, to use these approaches in humans, several important limitations must first be addressed, such as; selecting the proper immunodominant autoantigen; identifying the optimal timing, dosing and route of administration; finding biomarkers for monitoring the therapy; and optimizing methodology.

Indexed as

AutoantigensAutoimmune DiseasesFemaleHumansImmune ToleranceImmunosuppressive AgentsImmunotherapyMalePrognosisRheumatic DiseasesRisk AssessmentT-LymphocytesTreatment OutcomeAutoantigensImmunosuppressive Agents

Identifiers

PMID28701761
OpenAlexW2735687492

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.