
- Select a language for the TTS:
- UK English Female
- UK English Male
- US English Female
- US English Male
- Australian Female
- Australian Male
- Language selected: (auto detect) - EN
Play all audios:
The main function of the immune system in health is to protect the host from infection by microbes and parasites. Because immune responses to nonself bear the risk of unleashing accidental
immunity against self, evolution has endowed the immune system with central and peripheral mechanisms of tolerance, including regulatory T and B cells. Although the past two decades have
witnessed the successful clinical translation of a whole host of novel therapies for the treatment of chronic inflammation, the development of antigen-based approaches capable of selectively
blunting autoimmune inflammation without impairing normal immunity has remained elusive. Earlier autoantigen-specific approaches employing peptides or whole antigens have evolved into
strategies that seek to preferentially deliver these molecules to autoreactive T cells either indirectly, via antigen-presenting cells, or directly, via major histocompatibility complex
molecules, in ways intended to promote clonal deletion and/or immunoregulation. The disease specificity, mechanistic underpinnings, developability and translational potential of many of
these strategies remain unclear.
We thank the members of our laboratories for their contributions and insights. The authors’ work summarized here was funded by the Canadian Institutes of Health Research (CIHR), Diabetes
Canada, the Crohn’s and Colitis Foundation of Canada, the Multiple Sclerosis Society of Canada (MSSC), ISCIII and FEDER (PIE14/00027, PI15/0797), NEURON-ERANET (European Research Projects on
Neuroinflammation; NEURON7-FP-715-018), the Ministerio de Economia y Competitividad of Spain (MINECO) and Generalitat de Catalunya (SGR and CERCA Programmes). P. Serra was an investigator
of the Ramon y Cajal Re-integration Program and is supported by a JDRF Career Development Award. P. Santamaria was a Scientist of the Alberta-Innovates – Health Solutions (AI–HS) and a
scholar of the Instituto de Investigaciones Sanitarias Carlos III. The JMDRC was supported by the Diabetes Association (Foothills) and currently by Diabetes Canada.
Institut D’Investigacions Biomèdiques August Pi i Sunyer, Barcelona, Spain
Julia McFarlane Diabetes Research Centre (JMDRC) and Department of Microbiology, Immunology and Infectious Diseases, Snyder Institute for Chronic Diseases, Cumming School of Medicine,
University of Calgary, Calgary, Alberta, Canada
P. Santamaria is scientific founder of Parvus Therapeutics Inc. and has a financial interest in the company.
Publisher’s note: Springer Nature remains neutral with regard to jurisdictional claims in published maps and institutional affiliations.
Anyone you share the following link with will be able to read this content: