A Chromatin-Mimetic Nanomedicine for Therapeutic Tolerance Induction.
Bowen LiZhefan YuanPatrick McMullenJingyi XiePriyesh JainHsiang-Chieh HungShihan XuPeng ZhangXiaojie LinKan WuShaoyi JiangPublished in: ACS nano (2018)
The undesirable immune response poses a life-threatening challenge to human health. It not only deteriorates the therapeutic performance of biologic drugs but also contributes to various diseases such as allergies and autoimmune diseases. Inspired by the role of chromatin in the maintenance of natural immune tolerance, here we report a DNA-protein polymeric nanocomplex that can mimic the tolerogenic function of chromatin and induce an immune tolerance to its protein cargos. We first proved that the chromatin-mimetic nanomedicine loaded with keyhole limpet hemocyanin (KLH), a highly immunogenic model protein, could elicit a durable antigen-specific immune tolerance to KLH lasting for at least five weeks in mice. Following the proof-of-concept study, we demonstrated that this nanomedicine could be applied to improve the safety and efficacy of a biologic drug, PEGylated uricase, by attenuating the relevant antibody (Ab) responses. Moreover, we also demonstrated that prophylactic treatments with this nanomedicine could tolerize the immune system with the allergen of ovalbumin (OVA) and thus inhibit the occurrence of airway inflammation in an OVA-induced allergic asthma murine model. Collectively, our work illustrates a nature-inspired concept of immune tolerance induction and establishes a useful tool to specifically suppress unwanted immune responses for therapeutic purposes.
Keyphrases
- immune response
- cancer therapy
- gene expression
- dna damage
- human health
- risk assessment
- transcription factor
- genome wide
- drug delivery
- rheumatoid arthritis
- dendritic cells
- protein protein
- chronic obstructive pulmonary disease
- amino acid
- binding protein
- drug induced
- regulatory t cells
- type diabetes
- dna methylation
- lung function
- cystic fibrosis
- high glucose
- climate change
- high fat diet induced
- diabetic rats
- preterm birth