An antigen-less pro-vaccine for treating autoimmunity
We have designed the first antigen-less pro-vaccine, named 8206, for treating autoimmune diseases. Composed of dexamethasone, rapamycin, and R848 at a mass ratio of 8:20:6, 8206 is a complete tolerogenic adjuvant that acts systemically to form an active vaccine in situ with endogenous pathogenic autoantigens. This active vaccine suppresses autoimmunity by expanding antigen-specific Treg cells in affected tissues. In a mouse model of atherosclerosis, 8206 successfully targeted all three analyzed pathogenic autoantigens (ApoB, HSP60, and HMGB1) and inhibited disease progression. These findings suggest that 8206 can potentially serve as a universal treatment vaccine for autoimmune diseases by eliminating the need for exogenous immunogens, with implications for broad applications in immunotherapy.
Authors
- Thura Tun Oo
- Sunil Palani (ORCID: https://orcid.org/0000-0002-3990-0343)
- Sruthy Pallikonda Chakravarthy (ORCID: https://orcid.org/0009-0004-0936-3737)
- Aoshuang Chen
- Sri Sushma Santhi Janjam
- Guoxing Zheng (ORCID: https://orcid.org/0000-0002-1296-8727)
- Addysen Feng
- Christian ellis
- Amanda L. Williams (ORCID: https://orcid.org/0000-0003-1343-1101)
- Wallace Anthon
- Gwendolyn Tsaras
Institutions
- Illinois College (US)
- University of Illinois Chicago, Rockford campus (US)
- University of Virginia (US)
Publication Details
- Journal
- The Journal of Immunology
- Published
- 2025-04-24
- DOI
- https://doi.org/10.1093/jimmun/vkaf068
- Citations
- 1
- Primary Topic
- Atherosclerosis and Cardiovascular Diseases
- Type
- article
- Field-Weighted Citation Impact
- 0.80