Liposomal AntagomiR‐155‐5p Restores Anti‐Inflammatory Macrophages and Improves Arthritis in Preclinical Models of Rheumatoid Arthritis

Author:

Paoletti Audrey1ORCID,Ly Bineta1,Cailleau Catherine2,Gao Fan3,de Ponfilly‐Sotier Marie Péan1,Pascaud Juliette1,Rivière Elodie1,Yang Luxin4,Nwosu Lilian4,Elmesmari Aziza4,Reynaud Franceline2,Hita Magali2,Paterson David3,Reboud Julien3,Fay Francois2,Nocturne Gaetane15ORCID,Tsapis Nicolas2,McInnes Iain B.4ORCID,Kurowska‐Stolarska Mariola4,Fattal Elias2,Mariette Xavier15ORCID

Affiliation:

1. Paris‐Saclay University, INSERM UMR1184, Center for Immunology of Viral Infections and Autoimmune Diseases, Le Kremlin Bicêtre France

2. Université Paris‐Saclay, CNRS, Institut Galien Paris‐Saclay Orsay France

3. Division of Biomedical Engineering, James Watt School of Engineering, University of Glasgow Glasgow United Kingdom

4. School of Infection and Immunity, University of Glasgow Glasgow United Kingdom

5. Rheumatology Department, Hôpital Bicêtre, Assistance Publique – Hôpitaux de Paris Le Kremlin Bicêtre France

Abstract

ObjectiveWe previously reported an increased expression of microRNA‐155 (miR‐155) in the blood monocytes of patients with rheumatoid arthritis (RA) that could be responsible for impaired monocyte polarization to anti‐inflammatory M2‐like macrophages. In this study, we employed two preclinical models of RA, collagen‐induced arthritis and K/BxN serum transfer arthritis, to examine the therapeutic potential of antagomiR‐155‐5p entrapped within PEGylated (polyethylene glycol [PEG]) liposomes in resolution of arthritis and repolarization of monocytes towards the anti‐inflammatory M2 phenotype.MethodsAntagomiR‐155‐5p or antagomiR‐control were encapsulated in PEG liposomes of 100 nm in size and −10 mV in zeta potential with high antagomiR loading efficiency (above 80%). Mice were injected intravenously with 1.5 nmol/100 μL PEG liposomes containing antagomiR‐155‐5p or control after the induction of arthritis.ResultsWe demonstrated the biodistribution of fluorescently tagged PEG liposomes to inflamed joints one hour after the injection of fluorescently tagged PEG liposomes, as well as the liver's subsequent accumulation after 48 hours, indicative of hepatic clearance, in mice with arthritis. The injection of PEG liposomes containing antagomiR‐155‐5p decreased arthritis score and paw swelling compared with PEG liposomes containing antagomiR‐control or the systemic delivery of free antagomiR‐155‐5p. Moreover, treatment with PEG liposomes containing antagomiR‐155‐5p led to the restoration of bone marrow monocyte defects in anti‐inflammatory macrophage differentiation without any significant functional change in other immune cells, including splenic B and T cells.ConclusionThe injection of antagomiR‐155‐5p encapsulated in PEG liposomes allows the delivery of small RNA to monocytes and macrophages and reduces joint inflammation in murine models of RA, providing a promising strategy in human disease.image

Funder

Foundation for Research in Rheumatology

Publisher

Wiley

Subject

Immunology,Rheumatology,Immunology and Allergy

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