Therapy targeting antigen-specific T cells by a peptide-based tolerizing vaccine against autoimmune arthritis

Author:

Urbonaviciute Vilma1,Romero-Castillo Laura1ORCID,Xu Bingze1,Luo Huqiao1ORCID,Schneider Nadine2ORCID,Weisse Sylvia2ORCID,Do Nhu-Nguyen2ORCID,Oliveira-Coelho Ana1ORCID,Fernandez Lahore Gonzalo1ORCID,Li Taotao1ORCID,Sabatier Pierre3,Beusch Christian M.3,Viljanen Johan4,Zubarev Roman A.35ORCID,Kihlberg Jan4,Bäcklund Johan1,Burkhardt Harald26ORCID,Holmdahl Rikard1ORCID

Affiliation:

1. Division for Medical Inflammation Research, Department of Medical Biochemistry and Biophysics, Karolinska Institute 17177 Stockholm, Sweden

2. Fraunhofer Institute for Translational Medicine and Pharmacology ITMP 60596 Frankfurt am Main, Germany

3. Division of Physiological Chemistry I, Department of Medical Biochemistry and Biophysics, Karolinska Institute 17176 Stockholm, Sweden

4. Department of Chemistry-Biomedicinskt centrum (BMC), Uppsala University 752 37 Uppsala, Sweden

5. Department of Pharmacological & Technological Chemistry, I. M. Sechenov First Moscow State Medical University 119146 Moscow, Russia

6. Division of Rheumatology, University Hospital Frankfurt, Goethe University 60590 Frankfurt am Main, Germany

Abstract

A longstanding goal has been to find an antigen-specific preventive therapy, i.e., a vaccine, for autoimmune diseases. It has been difficult to find safe ways to steer the targeting of natural regulatory antigen. Here, we show that the administration of exogenous mouse major histocompatibility complex class II protein bounding a unique galactosylated collagen type II (COL2) peptide (A q –galCOL2) directly interacts with the antigen-specific TCR through a positively charged tag. This leads to expanding a VISTA-positive nonconventional regulatory T cells, resulting in a potent dominant suppressive effect and protection against arthritis in mice. The therapeutic effect is dominant and tissue specific as the suppression can be transferred with regulatory T cells, which downregulate various autoimmune arthritis models including antibody-induced arthritis. Thus, the tolerogenic approach described here may be a promising dominant antigen-specific therapy for rheumatoid arthritis, and in principle, for autoimmune diseases in general.

Funder

Knut och Alice Wallenbergs Stiftelse

Vetenskapsrådet

Reumatikerförbundet

Familjen Erling-Perssons Stiftelse

German Federal Ministry of Education and Research GO-Bio-project aidCURE

Federal State of Hesse (LOEWE-project 13, IME Fraunhofer Project Group TMP at Goethe University

Fraunhofer Cluster of Excellence for Immune-Mediated Diseases CIMD

Spanish Ministry of Universities through the European Union

Publisher

Proceedings of the National Academy of Sciences

Subject

Multidisciplinary

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