Bioconjugate Strategies for the Induction of Antigen-Specific Tolerance in Autoimmune Diseases.
Chunsong YuJingchao XiMeng LiMyunggi AnHaipeng LiuPublished in: Bioconjugate chemistry (2017)
Antigen-specific immunotherapy (ASI) holds great promise for the treatment of autoimmune diseases. In mice, administration of major histocompatibility complex (MHC) binding synthetic peptides which modulate T cell receptor (TCR) signaling under subimmunogenic conditions induces selective tolerance without suppressing the global immune responses. However, clinical translation has yielded limited success. It has become apparent that the TCR signaling pathway via synthetic peptide antigen alone is inadequate to induce an effective tolerogenic immunity in autoimmune diseases. Bioconjugate strategies combining additional immunomodulatory functions with TCR signaling can amplify the antigen-specific immune tolerance and possibly lead to the development of new treatments in autoimmune diseases. In this review, we provide a summary of recent advances in the development of bioconjugates to achieve antigen-specific immune tolerance in vivo, with the discussion focused on the underlying design principles and challenges that must be overcome to target these therapies to patients suffering from autoimmune diseases.
Keyphrases
- regulatory t cells
- signaling pathway
- immune response
- end stage renal disease
- dendritic cells
- chronic kidney disease
- ejection fraction
- newly diagnosed
- type diabetes
- computed tomography
- prognostic factors
- pi k akt
- toll like receptor
- epithelial mesenchymal transition
- metabolic syndrome
- inflammatory response
- adipose tissue
- patient reported outcomes
- big data
- patient reported
- transcription factor
- replacement therapy