λ-CO, an oligosaccharide with anti-inflammatory properties

Oligosaccharides that mimic heparan sulfate (HS) exhibit a variety of biological activities. One such oligosaccharide, λ-CO, a λ-carrageenan-derivative previously shown to inhibit cell migration, invasion, and heparanase 1 (HPA1), was evaluated for its anti-inflammatory properties. In LPS-stimulated macrophages, λ-CO significantly reduced Il-6 and Tnf-α production, as well as Erk and Akt phosphorylation, and Mmp-2/Mmp-9 secretion, independently of Hpa1 activity. In primary human keratinocytes stimulated with the psoriasis-mimicking M5 cytokine cocktail, λ-CO down-regulated cathepsin L and MMP-9 expression, as well as several M5-induced inflammatory genes. In vivo, λ-CO (1 and 10 mg.kg⁻¹) was administered in the imiquimod-induced mouse model of psoriasiform inflammation. Although no overt macroscopic improvement in skin lesions was evident, λ-CO at 10 mg.kg⁻¹ downregulated several inflammation-related genes in the skin and significantly reduced serum Mmp-9 levels. Taken together, these results suggest that λ-CO is a potential anti-inflammatory agent that selectively inhibits MMP-9 expression. This supports its further development as an adjunct to biotherapies for inflammatory skin disorders such as psoriasis.

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Publication Details

Journal
Biomedicine & Pharmacotherapy
Published
2026-01-06
DOI
https://doi.org/10.1016/j.biopha.2025.118954
Primary Topic
Proteoglycans and glycosaminoglycans research
Type
article
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article

λ-CO, an oligosaccharide with anti-inflammatory properties

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Biomedicine & Pharmacotherapy
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article

λ-CO, an oligosaccharide with anti-inflammatory properties

Jean‐François Jégou, Rachel Havret, Laure Favot-Laforge, Rachida Mersni-Achour, Laurent Picot, Kévin Baranger, Franck Morel, Benjamin Musnier, Valérie Thiéry, Damien Chassaing, Beatrice Colin, H. Groult, Jennifer Saliba, Manon Porta Zapata, Julien Cherfan, Clément Daviaud, Chanez Manseur, Hugo Main
article en

Abstract

Oligosaccharides that mimic heparan sulfate (HS) exhibit a variety of biological activities. One such oligosaccharide, λ-CO, a λ-carrageenan-derivative previously shown to inhibit cell migration, invasion, and heparanase 1 (HPA1), was evaluated for its anti-inflammatory properties. In LPS-stimulated macrophages, λ-CO significantly reduced Il-6 and Tnf-α production, as well as Erk and Akt phosphorylation, and Mmp-2/Mmp-9 secretion, independently of Hpa1 activity. In primary human keratinocytes stimulated with the psoriasis-mimicking M5 cytokine cocktail, λ-CO down-regulated cathepsin L and MMP-9 expression, as well as several M5-induced inflammatory genes. In vivo, λ-CO (1 and 10 mg.kg⁻¹) was administered in the imiquimod-induced mouse model of psoriasiform inflammation. Although no overt macroscopic improvement in skin lesions was evident, λ-CO at 10 mg.kg⁻¹ downregulated several inflammation-related genes in the skin and significantly reduced serum Mmp-9 levels. Taken together, these results suggest that λ-CO is a potential anti-inflammatory agent that selectively inhibits MMP-9 expression. This supports its further development as an adjunct to biotherapies for inflammatory skin disorders such as psoriasis.

Biomedicine & PharmacotherapyVol. 195
Centre National de la Recherche Scientifique (FR), Université de Poitiers (FR), La Rochelle Université (FR)
Openalex Percentile: Top 96%
Proteoglycans and glycosaminoglycans research
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