Engineering Immunological Tolerance Using Quantum Dots to Tune the Density of Self‐Antigen Display
Abstract
Treatments for autoimmunity—diseases where the immune system mistakenly attacks self‐molecules—are not curative and leave patients immunocompromised. New studies aimed at more specific treatments reveal that development of inflammation or tolerance is influenced by the form in which self‐antigens are presented. Using a mouse model of multiple sclerosis (MS), it is shown for the first time that quantum dots (QDs) can be used to generate immunological tolerance by controlling the density of self‐antigen on QDs. These assemblies display dense arrangements of myelin self‐peptide associated with disease in MS, are uniform in size (<20 nm), and allow direct visualization in immune tissues. Peptide‐QDs rapidly concentrate in draining lymph nodes, colocalizing with macrophages expressing scavenger receptors involved in tolerance. Treatment with peptide‐QDs reduces disease incidence tenfold. Strikingly, the degree of tolerance—and the underlying expansion of regulatory T cells—correlates with the density of myelin molecules presented on QDs. A key discovery is that higher numbers of tolerogenic particles displaying lower levels of self‐peptide are more effective for inducing tolerance than fewer particles each displaying higher densities of peptide. QDs conjugated with self‐antigens can serve as a new platform to induce tolerance, while visualizing QD therapeutics in tolerogenic tissue domains.
Document Details
- Document Type
- Pub Defense Publication
- Publication Date
- Apr 03, 2017
- Source ID
- 10.1002/adfm.201700290
Entities
People
- Christopher M Jewell
- Eunkeu Oh
- Igor L. Medintz
- James I Andorko
- Jeffrey R. Deschamps
- Kimihiro Susumu
- Krystina L. Hess
- Lisa H. Tostanoski
Organizations
- Alliance for Cancer Gene Therapy
- American Association of Pharmaceutical Scientists
- Astrophysics Science Division
- Damon Runyon Cancer Research Foundation
- Melanoma Research Alliance
- National Institutes of Health
- National Science Foundation
- United States Department of Veterans Affairs
- United States Naval Research Laboratory
- University of Maryland
- University of Maryland School of Medicine