# The Combination of Immunomodulatory Secretome and Liposome-Bound TRAIL Improves Knee Osteoarthritis Symptoms in an Ovine Model

**Authors:** Joaquín Marco-Brualla, Felícito García-Álvarez, Sara Fuente, Pablo Fernández, Arantza Vitoria, Francisco José Vázquez, Juan Pedro Lapuente-Fernández, Luis Martínez-Lostao, Antonio Romero, Alberto Anel

PMC · DOI: 10.3390/pharmaceutics18020193 · 2026-02-02

## TL;DR

A combination of two therapies improved knee osteoarthritis symptoms in a sheep model by reducing inflammation and joint damage.

## Contribution

The study demonstrates the efficacy of combining immunomodulatory secretome and liposome-bound TRAIL in treating osteoarthritis in an ovine model.

## Key findings

- The combined therapy significantly improved early-stage osteoarthritis parameters like synovial hyperplasia and tibial plateau damage.
- Synovial inflammation and imaging scores showed a tendency toward improvement with the combination treatment.
- X-ray and macroscopic assessments supported the positive effects of the combined therapy.

## Abstract

Background/Objectives: Knee osteoarthritis stands as the highest prevalent joint disease worldwide, affecting millions of adults and significantly impairing mobility and quality of life. Pro-inflammatory cells and cytokines are considered key players in the pathophysiology of the disease. In previous work, two anti-inflammatory therapeutic approaches were developed: a secretome enriched in anti-inflammatory cytokines, and nanoliposome-bound TRAIL (LUV-TRAIL), with proven efficacy against rheumatoid arthritis in rabbits. Methods: In this work, we evaluated the ability of these treatments to prevent the development of osteoarthritis (OA) in an ovine model following meniscectomies. Two weeks after the surgeries, knees were treated with several rounds of single or combined therapy, and then sheep were left untreated for several months. Knee damage was followed by X-ray analysis and, after sacrifice, assessed through macroscopic inspection, histological determinations, and inflammatory cytokine measurements. Results: The combined therapy had a significant positive effect against osteoarthritis development. Specifically, the combination is capable of improving knee injury in the first stages of OA in several parameters, such as synovial hyperplasia and tibial plateau damage, which are two of the most frequently damaged areas. Other markers, such as synovial inflammation and X-ray and macroscopic images, also presented a tendency to improved scores. Conclusions: The combination of the secretome with LUV-TRAIL represents a promising therapy worth exploring further in osteoarthritis treatment and/or prevention.

## Linked entities

- **Diseases:** osteoarthritis (MONDO:0005178), rheumatoid arthritis (MONDO:0008383)

## Full-text entities

- **Genes:** IL-4 [NCBI Gene 101122781], MCP-1 [NCBI Gene 443546], IFN-gamma [NCBI Gene 443396], IL-18 [NCBI Gene 443206], CDK9 [NCBI Gene 101109788], SCF [NCBI Gene 443371], MMP-1 [NCBI Gene 101120355], IL-10 [NCBI Gene 443342], IL-1alpha [NCBI Gene 443404], CSF1 (colony stimulating factor 1) [NCBI Gene 1435] {aka CSF-1, MCSF, PG-M-CSF}, IL-2 [NCBI Gene 443401], IL-1beta [NCBI Gene 443539], TTR (transthyretin) [NCBI Gene 7276] {aka AMYLD1, ATTR, CTS, CTS1, HEL111, HsT2651}, IP-10 [NCBI Gene 442997], Eotaxin [NCBI Gene 101119832], GM-CSF [NCBI Gene 443400], NF-kappaB [NCBI Gene 443119], AKT [NCBI Gene 100294652], IL-6 [NCBI Gene 443406], IL-7 [NCBI Gene 443341], LIF [NCBI Gene 101110180], VEGF-D [NCBI Gene 101102873], IL-27 [NCBI Gene 101122495], IGF-1 [NCBI Gene 443318], IL-9 [NCBI Gene 101105494], HGF [NCBI Gene 443075], FGF-2 [NCBI Gene 443306], IL-15 [NCBI Gene 443056], BDNF [NCBI Gene 101117275], MIP- [NCBI Gene 100294602], IL-22 [NCBI Gene 100885770], IL-5 [NCBI Gene 443350], TIMP-1 [NCBI Gene 443331], VEGF-A [NCBI Gene 443103], IL-17A [NCBI Gene 101103931], TNF [NCBI Gene 443540], IL-21 [NCBI Gene 100862657], MMP-3 [NCBI Gene 101118895], IL-8 [NCBI Gene 443418], IL-13 [NCBI Gene 664707]
- **Diseases:** fibrillations (MESH:D014693), joint destruction (MESH:D008105), Synovial Hyperplasia (MESH:D006965), meniscus trauma (MESH:D000070600), joint degeneration (MESH:D009410), bone-end deformities (MESH:D001847), plateau damage (MESH:D000092463), Knee Osteoarthritis (MESH:D020370), bone erosion (MESH:D014077), joint damage (MESH:D007592), cytotoxicity (MESH:D064420), erosions to subchondral bone (MESH:D001845), synovial damage (MESH:D013581), Knee damage (MESH:D007718), rheumatoid arthritis (MESH:D001172), Damage (MESH:D020263), Cartilage (MESH:D002357), OA (MESH:D010003), sclerosis (MESH:D012598), obesity (MESH:D009765), cancer (MESH:D009369), pain (MESH:D010146), injuries (MESH:D014947), degenerative disease (MESH:D019636), Inflammation (MESH:D007249), Fibrosis (MESH:D005355)
- **Chemicals:** formaldehyde (MESH:D005557), eosin (MESH:D004801), 1,2-distearoyl-sn-glycero-3-phosphoethanolamine)-N-(methoxy(polyethylene glycol)-2000) (MESH:C519184), alcohol (MESH:D000438), chloroform (MESH:D002725), LPS (MESH:D008070), Lipids (MESH:D008055), CO2 (MESH:D002245), phosphatidyl-choline (MESH:D010713), flavopiridol (MESH:C077990), doxorubicin (MESH:D004317), glycosaminoglycan (MESH:D006025), hematoxylin (MESH:D006416), Carazzi's Hematoxylin (-), safranin (MESH:C009195), sphingomyelin (MESH:D013109), H/E (MESH:D006371), ethanol (MESH:D000431), cholesterol (MESH:D002784), hyaluronic acid (MESH:D006820), bortezomib (MESH:D000069286), xylene (MESH:D014992), nitrogen (MESH:D009584), PTFE (MESH:D011138), paraffin (MESH:D010232), methanol (MESH:D000432)
- **Species:** Capra hircus (domestic goat, species) [taxon 9925], Oryctolagus cuniculus (domestic rabbit, species) [taxon 9986], Homo sapiens (human, species) [taxon 9606], Ovis aries (domestic sheep, species) [taxon 9940], Mus musculus (house mouse, species) [taxon 10090]

## Figures

11 figures with captions in the complete paper: https://tomesphere.com/paper/PMC12944125/full.md

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Source: https://tomesphere.com/paper/PMC12944125