Evidence map›Paper›PMID 41853281›Full record

ArticleFrontiers in immunology2026

Sex-associated transcriptional changes to synovial macrophages in the aging joint.

Matthew Dapas, Erica N DeJong, Yidan Wang, Cally Mills, Samuel D Dowling, Meghan L Mayer, Tyler Therron, Samuel D Hamilton, Carla M Cuda, Dawn M E Bowdish and 1 more

Abstract read
In one paragraph

Article in Frontiers in immunology, 2026. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 1 paper.

0numbers the graph read from it
0cells of the map it votes in
1citing 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

1 citing paper in PubMed.

  1. Article
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

11 authors.

Matthew DapasDivision of Rheumatology, Department of Pediatrics, Northwestern University Feinberg School of Medicine, Chicago, IL, United States.
Erica N DeJongDepartment of Medicine, McMaster University, Hamilton, ON, Canada.
Yidan WangDivision of Rheumatology, Department of Pediatrics, Northwestern University Feinberg School of Medicine, Chicago, IL, United States.
Cally MillsDivision of Rheumatology, Department of Pediatrics, Northwestern University Feinberg School of Medicine, Chicago, IL, United States.
Samuel D DowlingDivision of Rheumatology, Department of Pediatrics, Northwestern University Feinberg School of Medicine, Chicago, IL, United States.
Meghan L MayerDivision of Rheumatology, Department of Pediatrics, Northwestern University Feinberg School of Medicine, Chicago, IL, United States.
Tyler TherronDivision of Rheumatology, Department of Pediatrics, Northwestern University Feinberg School of Medicine, Chicago, IL, United States.
Samuel D HamiltonDivision of Rheumatology, Department of Pediatrics, Northwestern University Feinberg School of Medicine, Chicago, IL, United States.
Carla M CudaDivision of Rheumatology, Department of Pediatrics, Northwestern University Feinberg School of Medicine, Chicago, IL, United States.
Dawn M E Bowdish *Department of Medicine, McMaster University, Hamilton, ON, Canada.
Deborah R Winter *Division of Rheumatology, Department of Pediatrics, Northwestern University Feinberg School of Medicine, Chicago, IL, United States.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Background: Synovial macrophages are critical to tissue maintenance and immune homeostasis in the joints. However, the function of synovial macrophages is compromised with age, leading to increased susceptibility to chronic inflammation and arthritis. Here, we compare the transcriptional heterogeneity of synovial macrophages in young and old joints from male and female mice to better understand the impact of aging and the role of sex. Methods: We compared synovial macrophage composition and transcriptional profiles in young vs. old joints from male and female mice using single-cell RNA sequencing with cell-surface protein detection (CITE-seq). Results: We defined five major synovial macrophage subpopulations: CX3CR1+ lining, CD163+ interstitial, MHCII+ monocyte-derived, Ly6C+ infiltrating, and Conclusions: In summary, we report on both conserved age-related changes and those that differed between males and females. Our results provide insights on how macrophage heterogeneity changes with age in a sex-dimorphic manner and lays the foundation for research into their role in age-associated diseases, such as arthritis.

Indexed as

AgingJointsMacrophagesSynovial MembraneAnimalsFemaleMaleMiceMice, Inbred C57BLSex CharacteristicsSex FactorsTranscriptomeagingCITE-seqjointsmacrophagesynovial macrophages

Identifiers

PMID41853281
PMCPMC12992061

What OpenQuestion holds

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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.