#HowItWorks
We’ve designed our E-Vaccine to teach the body’s own immunity how it can destroy the virus permanently.
Or for more science minded visitors, we recommend these three publications to understand the methods of fabricating our vaccine, our solution to overcoming production of antibodies to conserved regions of HIV, and the potention for other applications of our platform technology.
- Reprint 1 JBC 2003 E-gp120 preparation (1)
- Reprint 2 AIDS 2014 E-gp120 solves Class switch problem (1)
- Reprint 3 Mech Aging Develp 2020 Catabody-IrAb-E-vaccine review 2020 (1)
Reprint 1 contains highlighted text (pages 2-3) concerning the method of HIV E-gp120 preparation. Reprint 2 describes the solution of the main impediment to inducing broadly neutralizing HIV antibodies. Reprint 3 is a brief review of our overall catabody/irreversible antibody/E-vaccine technology, including E-vaccine anti-aging potential when targeting amyloid targets.


Because of its electronically activated structure, the E-Vaccine programs the body’s immune cells to produce new types of antibodies: irreversible antibodies that bind HIV permanently, and catalytic antibodies – or abzymes – that destroy the virus coat.
Both irreversible antibodies and abzymes attack the mostly immutable part of the virus, thus prevent HIV from infecting white blood cells and replicating further.
Both irreversible antibodies and abzymes improve immune protection, an irreversible antibody because of its virtually ‘infinite’ binding affinity for the target, and an abzyme because it is cycled again and again to break many targets.
Sudhir Paul, Ph.D.
Ellen Cooper, M.D., MPH








