TOUCHED BY LYME: Why we care so strongly about a potential vaccine
by Dorothy Kupcha Leland
I was recently contacted by a reporter for a national news organization. She was blunt: why is your organization so opposed to a vaccine for Lyme disease?
Note, she didn’t say “what is your organization’s opinion about it?” or “are you opposed to it?” She re-stated several versions of this basic question: “why would an organization that is supposed to help Lyme patients be opposed to a vaccine that would protect people from Lyme disease?”
On the fast track
This comes as the French company Valneva SE is preparing for Phase 2 trials of its proposed Lyme vaccine, VLA-15. It has received fast-track designation from the FDA, which is a way of expediting the development of new drugs that are deemed to be especially needed.
It also comes on the heels of plenty of news coverage framing any discussion of a Lyme vaccine like this: A Lyme vaccine—any Lyme vaccine—is automatically a good thing. Anybody who raises any questions about it is a wicked “anti-vaxxer.” After all, look what those terrible people did to LYMErix.”
So, let me clarify a few points for the record.
LymeDisease.org is not “anti-vaccine.” Rather, we think important questions should be answered about the last Lyme vaccine before a new one is approved.
Plain and simple, we care about safety. The last vaccine, LYMErix, was introduced in 1998 and withdrawn from the market in 2002, after a number of serious problems cropped up.
- Over 1000 adverse events related to LYMErix were reported to the FDA, including death, strokes, musculoskeletal effects and neurologic effects.
- Over 400 people who felt they had been injured by the vaccine were preparing a class-action lawsuit against the manufacturer
- The last vaccine was not very effective. It required three doses given over the span of a year, to achieve less than 80% effectiveness.
- Furthermore, it was unclear whether booster shots would be required.
According to Valneva, VLA15 targets outer surface protein A (Osp A) of Borrelia, and
“the anticipated safety profile is expected to be similar to other vaccines using the same technology.”
Guess what? LYMErix was also based on Osp A. And its safety issues have never been appropriately addressed.
Here’s our bottom line: we want these concerns investigated and resolved before any new Lyme vaccine comes on the market.
There’s another matter as well. It’s becoming ever clearer that tick-borne diseases include many strains of Borrelia (not just Borrelia burgdorferi—what might be considered “classic” Lyme) along with other pathogens such as Babesia, Anaplasma/Ehrlichia, and Powassan virus.
An Osp A vaccine won’t do diddly-squat for co-infections.
Thus, we’re also concerned that a vaccine that only targets classic Lyme will give a false sense of security to those who receive it.
The market for a Lyme vaccine is projected to be between $800 million to $900 million a year.
I would think a company that stands to make that kind of money would cross their t’s and dot their i’s, in preparing the way for their product.
Yet, the manufacturers have not been forthright about safety issues with the previous vaccine. Nor have they reached out to the Lyme community in connection with this new one.
Here’s a thought: Valneva, why don’t you change your approach, starting right now? Answer our questions. See if you can allay our fears. It’s the right thing to do.
TOUCHED BY LYME is written by Dorothy Kupcha Leland, LymeDisease.org’s Vice-president and Director of Communications. She is co-author of When Your Child Has Lyme Disease: A Parent’s Survival Guide. Contact her at email@example.com .
Unfortunately, this infantile attack ploy against anyone who raises ANY questions about ANY vaccine is occurring as I write this sentence. It blows my mind how any professional gets away with name calling and bullying those questioning the safety of vaccines.
After all, much vaccine fraud has been uncovered recently, not to mention conflicts of interest.
Not to mention the fact only 1% of vaccine injuries are reported, of which independent researchers have stated the reporting system is “utterly inadequate,” and the CDC has even further thwarted the reporting process.
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