The tellurium-based immunomodulator, AS101 ameliorates adjuvant-induced arthritis in rats

Author:

Halpert G1ORCID,Halperin Sheinfeld M2,Monteran L23,Sharif K4,Volkov A5,Nadler R6,Schlesinger A78,Barshak I5,Kalechman Y2,Blank M1,Shoenfeld Y19ORCID,Amital H4

Affiliation:

1. Zabludowicz Center for Autoimmune Diseases, Sheba Medical Center, Tel Hashomer; Affiliated to Sackler Faculty of Medicine, Tel Aviv University, Tel Aviv, Israel

2. The Safdié Institute for Cancer, AIDS and Immunology Research; Faculty of Life Sciences, Bar-Ilan University, Ramat-Gan, Israel

3. Department of Pathology, Sackler Faculty of Medicine, Tel Aviv University, Tel Aviv, Israel

4. Internal Medicine B and Zabludowicz Center for Autoimmune Diseases, Sheba Medical Center, Tel Hashomer; Affiliated to Sackler Faculty of Medicine, Tel Aviv University, Tel Aviv, Israel

5. Institute of Pathology, Sheba Medical Center, Tel Hashomer; Sackler Faculty of Medicine, Tel-Aviv University, Tel-Aviv, Israel

6. The Academic Center of Law and Science, Hod Hasharon, Israel

7. Department of Geriatrics, Rabin Medical Center (Beilinson Campus), Petah Tikva, Israel

8. Sackler Faculty of Medicine, Tel Aviv University, Tel Aviv, Israel

9. Laboratory of the Mosaics of Autoimmunity, Saint Petersburg University, Saint Petersburg, Russian Federation

Abstract

Summary Despite undeniable improvement in the management of rheumatoid arthritis (RA), the discovery of more effective, less toxic and, ideally, less immune suppressive drugs are much needed. In the current study, we set to explore the potential anti-rheumatic activity of the non-toxic, tellurium-based immunomodulator, AS101 in an experimental animal model of RA. The effect of AS101 was assessed on adjuvant-induced arthritis (AIA) rats. Clinical signs of arthritis were assessed. Histopathological examination was used to assess inflammation, synovial changes and tissue lesions. Very late antigen-4 (VLA-4)+ cellular infiltration was detected using immunohistochemical staining. Enzyme-linked immunosorbent assay (ELISA) was used to measure circulating anti-cyclic citrullinated-peptide autoantibody (ACPA) and real-time polymerase chain reaction (PCR) was used to measure the in-vitro effect of AS101 on interleukin (IL)-6 and IL-1β expression in activated primary human fibroblasts. Prophylactic treatment with intraperitoneal AS101 reduced clinical arthritis scores in AIA rats (P < 0·01). AS101 abrogated the migration of active chronic inflammatory immune cells, particularly VLA-4+ cells, into joint cartilage and synovium, reduced the extent of joint damage and preserved joint architecture. Compared to phosphate-buffered saline (PBS)-treated AIA rats, histopathological inflammatory scores were significantly reduced (P < 0·05). Furthermore, AS101 resulted in a marked reduction of circulating ACPA in comparison to PBS-treated rats (P < 0·05). Importantly, AS101 significantly reduced mRNA levels of proinflammatory mediators such as IL-6 (P < 0·05) and IL-1β (P < 0·01) in activated primary human fibroblasts. Taken together, we report the first demonstration of the anti-rheumatic/inflammatory activity of AS101 in experimental RA model, thereby supporting an alternative early therapeutic intervention and identifying a promising agent for therapeutic intervention.

Funder

The Tovi Comet - Walerstein Cancer Research Chair

The Finkler Institute for Cancer, AIDS and Immunology Research

Publisher

Oxford University Press (OUP)

Subject

Immunology,Immunology and Allergy

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