Tolerogenic nanoparticles induce type II collagen–specific regulatory T cells and ameliorate osteoarthritis

Author:

Sohn Hee Su1ORCID,Choi Jeong Won2ORCID,Jhun JooYeon23ORCID,Kwon Sung Pil1ORCID,Jung Mungyo1ORCID,Yong Sangmin4ORCID,Na Hyun Sik35ORCID,Kim Jin-Hong4ORCID,Cho Mi-La26ORCID,Kim Byung-Soo178ORCID

Affiliation:

1. School of Chemical and Biological Engineering, Seoul National University, Seoul 08826, Republic of Korea.

2. The Rheumatism Research Center, Catholic Research Institute of Medical Science, The Catholic University of Korea, Seoul 06591, Republic of Korea.

3. Department of Biomedicine and Health Sciences, College of Medicine, The Catholic University of Korea, 222, Banpo-daero, Seocho-gu, Seoul 06591, Republic of Korea.

4. Department of Biological Sciences, College of Natural Sciences, Seoul National University, Seoul 08826, Republic of Korea.

5. Lab of Translational ImmunoMedicine, Catholic Research Institute of Medical Science, College of Medicine, The Catholic University of Korea, Seoul 06591, Republic of Korea.

6. Department of Medical Lifescience, College of Medicine, The Catholic University of Korea, 222, Banpo-daero, Seocho-gu, Seoul 06591, Republic of Korea.

7. Institute of Chemical Processes, Institute of Engineering Research, BioMAX, Seoul National University, Seoul 08826, Republic of Korea.

8. Interdisciplinary Program for Bioengineering, Seoul National University, Seoul 08826, Republic of Korea.

Abstract

Local inflammation in the joint is considered to contribute to osteoarthritis (OA) progression. Here, we describe an immunomodulating nanoparticle for OA treatment. Intradermal injection of lipid nanoparticles (LNPs) loaded with type II collagen (Col II) and rapamycin (LNP-Col II-R) into OA mice effectively induced Col II–specific anti-inflammatory regulatory T cells, substantially increased anti-inflammatory cytokine expression, and reduced inflammatory immune cells and proinflammatory cytokine expression in the joints. Consequently, LNP-Col II-R injection inhibited chondrocyte apoptosis and cartilage matrix degradation and relieved pain, while injection of LNPs loaded with a control peptide and rapamycin did not induce these events. Adoptive transfer of CD4 + CD25 + T cells isolated from LNP-Col II-R–injected mice suggested that T regs induced by LNP-Col II-R injection were likely responsible for the therapeutic effects. Collectively, this study suggests nanoparticle-mediated immunomodulation in the joint as a simple and effective treatment for OA.

Publisher

American Association for the Advancement of Science (AAAS)

Subject

Multidisciplinary

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