Evidence map›Paper›PMID 41798638›Full record

ReviewJournal of inflammation research2026

Non-Conventional and Emerging Autoantibodies in Sjögren's Disease.

Adrian Y S Lee

Abstract readReview
In one paragraph

Review in Journal of inflammation research, 2026. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.

0numbers the graph read from it
0cells of the map it votes in
0citing papers in PubMed
–field-weighted citation impact
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

0 citing papers in PubMed.

No citing paper in PubMed yet.

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

1 author.

Adrian Y S LeeDepartment of Clinical Immunology & Allergy, Westmead Hospital & ICPMR, Sydney, NSW, Australia.ORCID 0000-0002-5179-4803

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Sjögren's disease (SjD) is a chronic autoimmune disease that is characterised by dryness symptoms, arthralgias, systemic disease and B-cell hyperactivity. Serum autoantibodies are key pathological features of this disease. Anti-Ro52, anti-Ro60 and anti-La immunoglobulin G autoantibodies (sometimes known as antinuclear antibodies) are perhaps the most well-known autoantibodies, are important in the formal classification criteria for SjD and exist in up to 70% of patients. Rheumatoid factors, which are present in approximately 50% of patients, can reveal important prognostic information regarding the development of B-cell lymphomas. Beyond these autoantibodies, there are several emerging and novel autoantibodies associated with SjD that hold promise in identifying clinical features of SjD and facilitating the diagnosis of patients who lack the classic SjD-associated autoantibodies. These include anti-fodrin antibodies, anti-muscarinic acetylcholine receptor 3 antibodies and those autoantibodies traditionally associated with systemic lupus erythematosus. This narrative review article provides an updated review of these autoantibodies, discussing their potential clinical utility and the current limitations. Although many clinical associations have been identified, the routine clinical use of these autoantibodies is hampered by issues such as poor diagnostic sensitivity, contradictory associations, heterogeneous studies and small single-cohort studies. Further research using harmonised testing and large, multicentre cohorts is required to explore and validate the utility of these autoantibodies.

Indexed as

antibodiesautoantibodiesB cellsSjögren’s disease

Identifiers

PMID41798638
PMCPMC12967042

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Registered trials

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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.