Engineering antigens for in situ erythrocyte binding induces T-cell deletion

• Published in: Proceedings of the National Academy of Sciences - PNAS Vol. 110; no. 1; pp. E60 - E68
• Main Authors: Kontos, Stephan, Kourtis, Iraklis C., Dane, Karen Y., Hubbell, Jeffrey A.
• Format: Journal Article
• Language: English
• Published: United States National Academy of Sciences 02.01.2013; National Acad Sciences
• Series: PNAS Plus
• Subjects: Adoptive Transfer; Amino Acid Sequence; Analysis of Variance; Animals; antibodies; Antigens; Apoptosis; Apoptosis - immunology; autoantigens; Biological Sciences; Blood Glucose - metabolism; Blood Group Antigens - biosynthesis; Blood Group Antigens - metabolism; CD4-Positive T-Lymphocytes - immunology; CD8-Positive T-Lymphocytes - immunology; Clonal Anergy - immunology; Diabetes; Diabetes Mellitus - immunology; engineering; Erythrocytes; Erythrocytes - metabolism; Erythrocytes - physiology; Female; Flow Cytometry; genetically modified organisms; Glycophorin - metabolism; hepatocytes; insulin-dependent diabetes mellitus; Mice; Mice, Inbred C57BL; Mice, Transgenic; Molecular Sequence Data; Peptides; Peptides - genetics; PNAS Plus; Protein Engineering - methods; T cell receptors; T-lymphocytes
• ISSN: 0027-8424; 1091-6490; 1091-6490
• DOI: 10.1073/pnas.1216353110

Antigens derived from apoptotic cell debris can drive clonal T-cell deletion or anergy, and antigens chemically coupled ex vivo to apoptotic cell surfaces have been shown correspondingly to induce tolerance on infusion. Reasoning that a large number of erythrocytes become apoptotic (eryptotic) and are cleared each day, we engineered two different antigen constructs to target the antigen to erythrocyte cell surfaces after i.v. injection, one using a conjugate with an erythrocyte-binding peptide and another using a fusion with an antibody fragment, both targeting the erythrocyte-specific cell surface marker glycophorin A. Here, we show that erythrocyte-binding antigen is collected much more efficiently than free antigen by splenic and hepatic immune cell populations and hepatocytes, and that it induces antigen-specific deletional responses in CD4 ⁺ and CD8 ⁺ T cells. We further validated T-cell deletion driven by erythrocyte-binding antigens using a transgenic islet β cell-reactive CD4 ⁺ T-cell adoptive transfer model of autoimmune type 1 diabetes: Treatment with the peptide antigen fused to an erythrocyte-binding antibody fragment completely prevented diabetes onset induced by the activated, autoreactive CD4 ⁺ T cells. Thus, we report a translatable modular biomolecular approach with which to engineer antigens for targeted binding to erythrocyte cell surfaces to induce antigen-specific CD4 ⁺ and CD8 ⁺ T-cell deletion toward exogenous antigens and autoantigens.