Evidence map›Paper›PMID 42488662›Full record

ArticleFrontiers in immunology2026

Synovial fluid IL-16 and RANTES/CCL5 signals in early knee osteoarthritis: a pilot antibody-array study.

Bei Lin, Boyue Wu, Huihuang Chen, Wentao Lin, Dasheng Lin, Eryou Feng

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Article in Frontiers in immunology, 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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1 · What the graph read from it

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3 · Its place in the literature

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4 · The record

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5 · Who and what money

Authors and funding

6 authors.

Bei Lin *Department of Orthopedic Surgery, Fujian Medical University Union Hospital, Fuzhou, China.
Boyue Wu *Department of Orthopedic Surgery, Fujian Medical University Union Hospital, Fuzhou, China.
Huihuang ChenDepartment of Orthopedic Surgery, Fujian Medical University Union Hospital, Fuzhou, China.
Wentao LinDepartment of Orthopedic Surgery, Fujian Medical University Union Hospital, Fuzhou, China.
Dasheng LinDepartment of Orthopedic Surgery, Fujian Medical University Union Hospital, Fuzhou, China.
Eryou FengDepartment of Orthopedic Surgery, Fujian Medical University Union Hospital, Fuzhou, China.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Background: Reliable molecular indicators for early osteoarthritis (OA) remain limited. Because synovial fluid (SF) reflects the intra-articular immune microenvironment, inflammatory signals may help describe preliminary features associated with early OA for future validation. This pilot, hypothesis-generating study used a high-throughput antibody array to profile SF cytokines across radiographic groups of knee OA. Methods: Sixteen participants were included: a K-L grade 0 non-radiographic comparator group (K0, n = 4), early OA (K1; Kellgren-Lawrence grade 1-2, n = 6), and late OA (K3; grade 3-4, n = 6). Forty inflammatory proteins were measured using the RayBiotech Human Inflammation Antibody Array. Results: In K1 versus K0, IL-16 [fold change (FC) = 15.79; logFC = 3.98; approximate Conclusions: In this very small pilot cohort, IL-16 and RANTES/CCL5 showed array-based inflammatory signals associated with early OA after multiple-testing correction. The findings do not constitute validation of a clinical marker, and no diagnostic claim is made because ELISA confirmation, ROC analysis, and an independent validation cohort were not available. These data should therefore be regarded as preliminary discovery results, and larger, adequately powered studies with orthogonal quantitative validation are required before clinical translation can be considered.

Indexed as

Chemokine CCL5Interleukin-16Osteoarthritis, KneeSynovial FluidAgedBiomarkersFemaleHumansMaleMiddle AgedPilot ProjectsProtein Array AnalysisBiomarkersCCL5 protein, humanChemokine CCL5Interleukin-16antibody arrayCCL5/RANTEScytokineshypothesis-generating analysisIL-16osteoarthritispilot studysynovial fluid

Identifiers

PMID42488662
PMCPMC13388094

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