Anti-Idiotypic MRNA Vaccine to Treat Autoimmune Disorders
Overview
Authors
Affiliations
The 80+ existing autoimmune disorders (ADs) affect billions with little prevention or treatment options, except for temporary symptomatic management, leading to enormous human suffering and a monumental financial burden. The autoantibodies formed in most ADs have been identified, allowing the development of novel anti-idiotypic antibodies to mute the autoantibodies using vaccines. Nucleoside vaccines have been successfully tested as antigen-specific immunotherapies (ASI), with mRNA technology offering multi-epitope targeting to mute multiple autoantibodies. This paper proposes using mRNA technology to produce anti-idiotypic antibodies with broad effectiveness in preventing and treating them. This paper delves into the state-of-the-art mRNA design strategies used to develop novel ASIs by selecting appropriate T cell and B cell epitopes to generate anti-idiotypic antibodies. The low cost and fast development of mRNA vaccines make this technology the most affordable for the global control of ADs.
Justiz-Vaillant A, Soodeen S, Gopaul D, Arozarena-Fundora R, Thompson R, Unakal C Microorganisms. 2025; 13(2).
PMID: 40005649 PMC: 11858333. DOI: 10.3390/microorganisms13020282.
Niazi S, Magoola M Int J Mol Sci. 2024; 25(23).
PMID: 39684504 PMC: 11641290. DOI: 10.3390/ijms252312797.
The role of autoantibodies in bridging obesity, aging, and immunosenescence.
Valentino T, Chen N, Makhijani P, Khan S, Winer S, Revelo X Immun Ageing. 2024; 21(1):85.
PMID: 39616399 PMC: 11607830. DOI: 10.1186/s12979-024-00489-2.
Progress and prospects of mRNA-based drugs in pre-clinical and clinical applications.
Shi Y, Shi M, Wang Y, You J Signal Transduct Target Ther. 2024; 9(1):322.
PMID: 39543114 PMC: 11564800. DOI: 10.1038/s41392-024-02002-z.
Pawar Y, Thool A Cureus. 2024; 16(8):e67078.
PMID: 39286691 PMC: 11405085. DOI: 10.7759/cureus.67078.