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This is a very exciting time in the history of vaccine production.

An absolute avalanche of DNA vaccines are being produced for the first time in history for many various diseases.

These are vaccines in which actual DNA is injected into animal or human bodies.

This DNA is carefully manufactured to then go into the cells into which it is injected and begin producing proteins that stimulate immune responses by the body.

Countless millions more elsewhere in the world suffer from this problem.

What IS known is that the many Herpes vaccines that have been produced, almost without exception, generate very strong immune responses in the animals and humans to which they are given.

For example, the injected DNA might cause the body to produce the “G antigen” of Herpes Simplex Type 2. A scientific paper published in early 1999 studying Herpes infections in mice found that a new DNA vaccine causing production of a certain herpes virus protein modified with bupivicaine in fact caused perhaps a 99% reduction in the ability to infect mice with “Herpes challenges” in the vaginas of the mice.

This antigen (which is only a tiny, tiny portion of the virus membrane and does NOT cause any sort of infection) stimulates an intense production of antibody against the “G antigen” of HSV2. The DNA vaccine efforts for GHI are only just now being explored and are probably 3 or 4 years away from substantial information being generated. This is, perhaps, the most encouraging evidence to date that in the not too distant future, a vaccine will be produced against genital herpes infections that will at least dramatically reduce the transmission of Herpes, if not virtually eliminate it.

Both vaccines are available for those interested, but one might have to travel to that country to take it.

The Bottom Line: There MAY be some benefit from these vaccines to reducing recurrence frequency.

So, if HSV2 shows up anywhere in the body, presumably the antibody produced by the body will knock out the HSV2. Will these vaccines (1) prevent recurrences, and (2) prevent transmission to non-infected partners? However, human test results have not as yet achieved the same results.

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