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COMPREHENSIVE IMMUNOPROFILING OF PERIPHERY BLOOD IDENTIFIES KEY IMMUNE FEATURES ASSOCIATED WITH DISEASE PROGRESSION AND PATIENT STRATIFICATION OF SLE

2025· article· en· W4410513002 on OpenAlexvenueno aff
Junna Ye, Zhuochao Zhou, Jingyi Wu, Chengde Yang

Bibliographic record

VenueThe Journal of Rheumatology · 2025
Typearticle
Languageen
FieldMedicine
TopicSystemic Sclerosis and Related Diseases
Canadian institutionsnot available
Fundersnot available
KeywordsMedicineStratification (seeds)Risk stratificationImmune systemDiseaseImmunopathologyImmunologyPathologyInternal medicine

Abstract

fetched live from OpenAlex

PV242 / #5 Poster Topic: AS23 - SLE-Diagnosis, Manifestations, & Outcomes Background/Purpose To advance the development of immune biomarkers for diagnosing and treating Systemic Lupus Erythematosus (SLE), we have established a robust evaluation platform that integrates immune repertoire sequencing, T cell subtype profiling, and transcriptional sequencing. Methods This platform facilitates a systematic exploration of the peripheral immune status of SLE patients, such as TCR, BCR, bulk Rnaseq and flow cytometry. Then we compare these immune characteristics with status of SLE patients, which are associated with their clinical conditions (Figure 1). Figure 1. The flowchart of this study. Results Notably, we observed significant clonal expansion, loss of naive T cells, and heightened activation and stress in both CD8+ and CD4+ T cells, suggesting a critical role of T cells in the pathogenesis of SLE. Furthermore, our analysis identified unique features in the immune repertoires of SLE patients compared to healthy donors, such as differential TRV-TRJ usage and the presence of public clones, which could serve as early diagnostic markers for SLE. For B cells, we identified a notable isotype switching and a prevalent usage of IgHV-IgHJ gene segments. This finding highlights the dynamic adaptability of the B cell compartment in response to autoimmune challenges. By integrating several immune indices, we have developed a novel approach to categorize SLE patients into groups based on their adaptive immune activity, which shows a partial correlation with their disease status (Figure 2). Moving forward, we aim to amalgamate all gathered immune profiling data and apply cutting-edge analytical techniques, including machine learning, to discern various immunotypes. Figure 2. The model to categorize SLE patients into groups based on their adaptive immune activity. Conclusions This stratification will enhance our ability to diagnose and tailor treatments for SLE patients to achieve favorable prognosis. Our study not only sheds light on the complexities of the immune system in SLE but also demonstrates the potential of comprehensive immunoprofiling in enhancing patient management in this challenging autoimmune disorder.

Fetched live from OpenAlex and de-inverted. Abstracts are not stored in this database: the inverted indexes are 8.6 GB of the frame’s 9.3 GB of text, and the host has 13 GB free.

How this classification was reachedexpand

Full frame machine prediction

Teacher imitation

Not calibrated prevalence, not ground truth. Human validation pending. The Gemma side is a direct model label for every work in the frame, read from the title-only record. The Codex side is a classifier learned from the 10,348 direct Codex labels and calibrated to design-weighted sample rates; fields without enough sample support carry no Codex call. Candidate is the union of the two sides; consensus is their intersection. These outputs are machine_predicted_unvalidated and are not human labels.

metaresearch head score (Codex)0.000
metaresearch head score (Gemma)0.000
Version: metacan-v3-hybrid-931329e0061cValidation status: machine_predicted_unvalidated
Candidate categoriesnone
Consensus categoriesnone
DomainCandidate signal: none · Consensus signal: none
Study designCandidate signal: Observational · Consensus signal: Observational
GenreCandidate signal: Empirical · Consensus signal: Empirical
Teacher disagreement score0.002
Threshold uncertainty score0.008

Distilled classifier scores by category (both heads)

CategoryCodexGemma
Metaresearch0.0000.000
Meta-epidemiology (narrow)0.0000.000
Meta-epidemiology (broad)0.0000.000
Bibliometrics0.0010.001
Science and technology studies0.0000.000
Scholarly communication0.0010.000
Open science0.0000.000
Research integrity0.0000.000
Insufficient payload (model declined to judge)0.0020.001

Machine scores (provisional)

The two teacher heads of the student model, read on this work. A score orders the frame for review; it never asserts a category, and the validation status ships verbatim with every row.

Baseline scores from an immature model (maturity gate not passed, 7 training rounds). Scores rank; they never assert a category.

Opus teacher head0.009
GPT teacher head0.256
Teacher spread0.247 · how far apart the two teachers sit on this one work
Validation statusscore_only:v0-immature-baseline · verbatim from the scoring run: score_only means the number may rank works, and no category label ships from it

Classification

machine, unvalidated

Machine predicted; a candidate call from one source (direct Gemma or distilled Codex), not a consensus.

The models applied no category: nothing in the taxonomy fit this work.
Study designObservational
Domainnot available
GenreEmpirical

How this classification was reached, model by model and score by score, is at the end of the page under "How this classification was reached".

Quick stats

Citations0
Published2025
Admission routes1
Has abstractyes

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