Evidence map›Paper›PMID 42004628›Full record

ArticleJournal of translational autoimmunity2026

Longitudinal evolution of rheumatoid factor-expressing lymphoma precursors in a patient with Sjögren's disease.

Adrian Y S Lee, Jing Jing Wang, David A Brown, Joanne H Reed

Abstract read
In one paragraph

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

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0citing papers in PubMed
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1 · What the graph read from it

What it found

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2 · The registry

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3 · Its place in the literature

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4 · The record

Corrections and comments

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5 · Who and what money

Authors and funding

4 authors.

Adrian Y S LeeCentre for Immunology and Allergy Research, Westmead Institute for Medical Research and Faculty of Medicine and Health, The University of Sydney, Westmead, NSW, Australia.
Jing Jing WangCollege of Medicine and Public Health, Flinders Health and Medical Research Institute, Flinders University, Bedford Park, SA, Australia.
David A BrownCentre for Immunology and Allergy Research, Westmead Institute for Medical Research and Faculty of Medicine and Health, The University of Sydney, Westmead, NSW, Australia.
Joanne H ReedCentre for Immunology and Allergy Research, Westmead Institute for Medical Research and Faculty of Medicine and Health, The University of Sydney, Westmead, NSW, Australia.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Objective: Patients with Sjögren's disease (SjD) have an increased risk of developing B cell lymphomas, which may express rheumatoid factors (RhF). However, it remains unclear whether RhF-secreting cells undergo malignant transformation. To address this question, we longitudinally tracked the evolution of a RhF clone in a rare SjD case before and after lymphoma diagnosis. Methods: Peripheral blood B cells, serum and malignant lymph node biopsy were collected from a 68-year-old male with SjD who developed diffuse large B cell lymphoma (DLBCL). Clonal RhF sequences were identified in serum by mass spectrometry and in B cells by mRNA sequencing. Recombinant IgM were generated from clonal sequences and assessed for RhF activity and cryoaggregation. Results: A monoclonal RhF was detected in serum and circulating B cells six months before DLBCL diagnosis. The same clone was expressed by the lymphoma. Clonal analysis demonstrated divergence into two branches: one with seven antibody mutations expressed by blood B cells, and a second with twelve antibody mutations in the serum RhF and lymphoma. Recombinant IgM representing the blood and serum RhF demonstrated RhF activity, whereas the lymphoma clone acquired three additional mutations that impaired RhF binding. Conclusions: Our prospective and longitudinal analyses provide direct evidence for a RhF secreting clone evolving into a lymphoma in a SjD patient. This work expands on previous cross-sectional studies of RhF expressing lymphomas in SjD and provides a proof-of-concept case, which potentially supports early therapeutic targeting of expanded RhF clones.

Indexed as

AutoantibodyCryoglobulinLymphomaRheumatoid factorSjögren's disease

Identifiers

PMID42004628
PMCPMC13091411

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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.