SAN FRANCISCO, April 3, 2017 -- In the ultimate betrayal, one's own immune system can turn against the protective sheath that envelops neurons in the brain, leaving the body paralyzed. Researchers have developed an experimental treatment that tames the wayward immune system in rodents, returning the power of movement to paralyzed mice. The approach may someday combat autoimmune diseases, such as multiple sclerosis and type 1 diabetes, in humans.
The researchers will present their work today at the 253rd National Meeting & Exposition of the American Chemical Society (ACS). ACS, the world's largest scientific society, is holding the meeting here through Thursday. It features more than 14,000 presentations on a wide range of science topics.
A brand-new video on the research is available at http://bit.
"The problem with current immunotherapies is that they aren't specific," says Christopher Jewell, Ph.D. "They act broadly, compromising the entire immune system and putting the patient's health at risk, rather than focusing on only those immune system cells doing the damage."
By considering how the immune system works, Jewell's team at the University of Maryland set their sights on the lymph nodes as a possible target for creating a specific immune response. In autoimmune disease, a body-roaming immune cell recognizes an antigen -- a molecule that the cell in this case falsely identifies as a piece of a foreign invader -- and brings it to the lymph nodes, where another type of immune cell, the T cell, is then programmed to attack the antigen. For example, in multiple sclerosis, T cells are taught to recognize and attack the myelin sheath. Jewell thought it might be possible to prevent the T cells from learning bad habits by delivering an immune-system modifying agent directly to the lymph nodes.
To build the immunotherapeutic agent, the researchers first constructed a particle from poly(lactide-co-glycolide), an FDA-approved polymer, to serve as a carrier. They infused it with an immune-suppressing agent and the myelin antigen, to teach the T cells that myelin is no enemy.
The researchers injected these particles into the lymph nodes of paralyzed mice exhibiting a mouse model of multiple sclerosis. The particles slowly reprogrammed the environment of the lymph node tissues to generate immune cells that migrated to the brain to stop the attack against myelin. These mice regained the ability to walk, and the effects lasted for the duration of the study, which was about 80 days. The mice were also able to readily respond when foreign molecules were introduced, suggesting that the treatment didn't compromise normal immune function.
As a next step, the researchers have been testing the idea in other mouse models of autoimmune disease, including transplant models and models of type 1 diabetes -- a disease in which the immune system attacks the pancreas. Later this year, the group will team up with clinicians at the University of Maryland Medical School to begin tests in non-human primates, another step closer to investigating this idea as a future human therapy.
A press conference on this topic will be held Monday, April 3, at 10 a.m. Pacific time in the Moscone Center. Reporters may check-in at the press center, South Building, Foyer, or watch live on YouTube http://bit.
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Harnessing biomaterials to study and engineer lymph node function
Vaccines and immunotherapies have generated some of the largest impacts on human health in history, but a challenge facing the field is how to direct the specific properties of immune responses that are elicited. This talk will highlight two strategies we are developing to study and exploit the interactions between biomaterials and immune tissues to enable more specific control of immune function. One approach involves direct delivery of synthetic vaccine carriers to lymph nodes (LNs), key tissues that coordinate immune response. We have combined direct LN injection with biomaterials to establish a platform to study the link between local LN function and systemic immunity by probing the roles of signal density and material properties. We are also exploiting this direct delivery for therapeutic vaccination to combat autoimmunity. In mouse models of multiple sclerosis, a single injection at the peak of disease shifts the LN microenvironment towards tolerance, permanently reversing paralysis without compromising normal immune function. The second focus area is the design of new modular materials we have created using polyionic immune signals to form stable capsules self-assembled entirely from immune signals. These immune polyelectrolyte multilayers (iPEMs) co-localize signals to draining LNs after injection, and allow selective activation or deactivation of inflammatory pathways (e.g., toll-like receptors) without carrier components such as polymers. iPEMs built from antigen and toll-like receptor (TLR) agonists enhance dendritic cell function, expand antigen-specific T cells, and provide protection during mouse tumor challenge. In contrast, iPEMs assembled from antigen and suppressive TLR ligands promote tolerance in mouse cells, mouse models of MS, and samples from human MS patients. Ultimately, these strategies could contribute to better understanding of the interactions between biomaterials and the immune system, and improve the rational design of materials that serve not only as carriers, but also as agents that actively direct immune response.