Feb. 19, 2016
Medical researchers discover new approach to treating autoimmune diseases
Researchers have developed a new class of nanomedicines to treat autoimmune diseases.
Riley Brandt, 91快色
A new study from the 91快色 could change the way researchers understand and treat autoimmune diseases such as type 1 diabetes, multiple sclerosis and rheumatoid arthritis.
The complexities of these diseases have made it very difficult to develop treatments that can stop disease without impairing normal immunity. Using animal models and human cells in animal models, researchers at the university鈥檚 Cumming School of Medicine have discovered a novel mechanism that stops the immune attack, and have developed a new class of drugs that harnesses this mechanism to treat various autoimmune diseases without compromising the entire immune system. The study is published in the February edition of the prestigious journal .
鈥淭his discovery is significant because we now know how to stop autoimmune diseases in a highly specific manner without compromising immunity in general,鈥 says Dr. Pere Santamaria, a professor in the Department of Microbiology, Immunology and Infectious Diseases, and member of the university鈥檚 .
More than 80 autoimmune diseases affect people around the world, including millions of Canadians. In these diseases, white blood cells, normally responsible for warding off foreign invaders like bacteria and viruses, sometimes mistakenly attack the body鈥檚 own "good" cells, causing their destruction. Each specific autoimmune disease results from an attack against thousands of individual protein fragments in the targeted organ, such as the insulin-producing pancreatic cells in the case of type 1 diabetes.
The study is led by Dr. Pere Santamaria (top).
Riley Brandt, 91快色
Nanoparticles used as 'bait' to reprogram disease-causing cells
Santamaria鈥檚 study shows that nanoparticles (particles thousands of times smaller than a typical cell), decorated with protein targets acting as "bait" for disease-causing white blood cells, can be used to reprogram them to suppress the disease they intended to cause. This new class of drugs (nanomedicines called Navacims) exploits a naturally occurring process, previously unknown to science, that is wired into our immune system to protect us against autoimmune disease.
Santamaria has shown that this mechanism and the nanomedicines that exploit it can be applied to several, and potentially all, autoimmune diseases in animals, by simply changing the bait on the nanoparticles. The study also shows that this mechanism operates in animals transplanted with human white blood cells, which essentially responded to the corresponding nanomedicines like their mouse counterparts.
In order to treat autoimmune diseases, most of the white blood cells directed against each of these targets need to be"鈥榯aken out"; however, many remain unknown. Current drugs have no way of distinguishing rogue white blood cells from normal ones and as a result, drugs used to treat these diseases also suppress normal immunity leaving the individual susceptible to other illnesses.
鈥淚magine if you wanted to stop a war,鈥 says Santamaria. 鈥淵ou would probably want to take out the entire army, which is what current drugs try to do.鈥 He notes that this new class of drugs deals with this problem from a completely different perspective 鈥淩ather than taking soldiers out, our drugs trick a single soldier into becoming the 鈥榯raitor鈥 that takes out the army general.鈥 He adds, 鈥淲ithout the general, the army ceases to operate and the war ends.鈥
Santamaria鈥檚 new drugs are currently being developed for the treatment of specific human autoimmune diseases by Parvus Therapeutics, Inc., a biotechnology company he founded with Innovate 91快色.
Pere Santamaria is Chair of the Julia McFarlane Diabetes Researcher Centre at the 91快色. He is a professor in the Department of Microbiology, Immunology and Infectious Diseases and a member of the Snyder Institute for Chronic Diseases in the Cumming School of Medicine. He is also group leader at Institut D鈥橧nvestigacions Biom猫diques August Pi i Sunyer, which also played a critical role in the study.
The study was funded by The Canadian Institutes of Health Research, the Canadian Diabetes Association, the Juvenile Diabetes Research Foundation, the Diabetes Research Foundation, the Multiple Sclerosis Society of Canada, the European Association for the Study of Diabetes, the Brawn Family Foundation, the National Research Council of Canada-Industrial Research Assistance Program, and the Instituto de Investigaciones Sanitarias Carlos III form the Spanish Ministry of Economy and Competitiveness.