Last Updated on 9th January 2020 by Caroline Haye
Will vitiligo cure be a magic bullet?
Last month I wrote about the exciting progress Dr John Harris and his team at the Vitiligo Clinic and Research Center (University of Massachusetts Medical School) are making towards an effective treatment for vitiligo. In particular, I celebrated Dr Harris’ unequivocal assertion that the damage caused to pigment cells in vitiligo is fully reversible. To me, this fact alone is more thrilling than any details about the skin re-pigmentation drugs currently being trialled.
I found it thrilling because it reinforces my own experience of vitiligo reversal. And because it confirms that it is no longer a question of whether there will be a cure… But rather when. The fact that clinical trials are actually going on now is obviously exciting news. As is the prospect that the first generation of drugs is likely to emerge within the next couple of years.
Vitiligo drugs will be a godsend to millions
These medications promise to be a godsend to millions of people around the world. Especially to those for whom pigment loss is psychologically devastating and socially disabling. Getting rid of the white patches that are the only obvious sign of illness in vitiligo has been a shared dream for countless sufferers, therapists and researchers alike. And it now seems highly likely this dream will become reality within the next few years.
I, for one, am very happy at this prospect. It has the potential to change the lives of an estimated 1- 2% of the world’s population for the better. And, whilst my own vitiligo has virtually disappeared, I am always aware that the condition could return. In fact, I am sure it would if I were to stop the nutritional therapy that has reversed it or else expose myself to certain triggers.
Research so far has identified what appears to be the core pathway for the development of vitiligo. Apparently, this involves destructive autoimmune activity and an abnormality of the melanocytes (pigment cells).
The research so far
The aim of the research is to pinpoint the process by which the immune system attacks melanocytes, as opposed to other parts of the body, and turn that particular “switch” off without deactivating the whole immune system. But Dr Harris makes no secret of the fact that these initial medications will not offer a perfect cure.
If I understand what I have read on this subject correctly, it is not yet possible to produce a drug that targets the autoimmune threat to pigment cells with pinpoint precision. So the best that can be expected of the first wave of medications is that they will halt and reverse vitiligo but may also increase susceptibility to certain other conditions such as shingles.
What do we mean by “a real cure”?
This begs the question: what do we really mean when we talk about a vitiligo cure? So-called magic bullets rarely, if ever, perform perfect medical miracles. Drugs usually come with various limitations, side effects or other drawbacks… Drawbacks that may or may not later be minimised through ongoing research and development.
And, of course, they always come at a price. Because medical research is an expensive business and pharmaceutical companies are not generally known for their charitable work. So, optimistic though I am, I am also aware that the first new treatments your doctor is likely to prescribe for your vitiligo will not be perfect and they will not be cheap.
In a sense, you could say that this is no different from the current state of affairs. We already have access to numerous imperfect vitiligo treatments and none of them (except for sun exposure) is free. So, as long as the new drugs prove to be better at re-pigmenting vitiligo than current options, then at least they will provide a cosmetic solution to the problem. And that is good.
But I very much hope that vitiligo research will not stop there. Because I do not believe that eradicating skin de-pigmentation is necessarily the same thing as curing a patient. And, as patients, I think we need to be aware of that concept. Otherwise, we may find ourselves relinquishing all responsibility for our wider health. I believe we will still need to ask two important questions: what caused the pigment loss in the first place; and has the drug fixed that?
Curing white patches or curing people?
Five years ago I posed the question: is vitiligo a disease or a symptom? If it is a disease, then any treatment that succeeds in permanently eradicating de-pigmentation will, deservedly, be hailed as a cure. But if it is (as I believe) a symptom, then it will only have succeeded in providing a cosmetic solution. It will not have addressed the reason for the symptom.
And, whilst that would still be a life-changing achievement for millions, it could also present additional risks, aside from the kinds of side-effects that might be considered acceptable (like the odd case of shingles).
Not being a scientist myself, I can only use my common sense and limited knowledge to speculate on these risks. But an increased susceptibility to various pathogens (and maybe not just minor ones) is evidently one. For another, I imagine that blocking autoimmune attacks against melanocytes is not the same thing as curing autoimmune disease. So it might cause the immune system to redirect its attacks to other healthy cells instead.
And, as I indicated earlier, eradicating a symptom like pigment loss may be a bit like removing the safety warning signs from a faulty piece of equipment. It may give us a false sense of security about the state of our health.
Am I pouring cold water on vitiligo drugs?
Am I pouring cold water on the prospect of a “vitiligo cure”? No -absolutely not. It is what I have spent the major portion of my life hoping and praying for. And I am still eagerly looking forward to the day when doctors will be able to offer vitiligo patients a reliable way of reversing their pigment loss. But I am just sounding a warning note that using drugs purely to return the skin to its normal colour will not necessarily be the same thing as restoring vitiligo patients to full health.
Experts agree that vitiligo is a multifactorial condition. In other words, a complex combination of factors contribute to its development. And these may not even be the same in every case. For myself, and many others I have come into contact with over the past several years, one underlying cause of our vitiligo would seem to be poor nutritional absorption, due to digestive abnormalities. And these will still need attending to if we want to be free of all autoimmune diseases and enjoy full health.
So, on the one hand, I am very excited to think that we are about to enter a pioneering stage in medical vitiligo treatment. But, on the other, I anticipate that the underlying health problems that cause de-pigmentation in the first place will still need attention before any medications can truly be called a perfect cure.
6 thoughts on “Skin re-pigmentation drugs”
Absolutely, Gosta – roll on that day!
Tengo vitíligo desde hace 45años me hecho todo lo que me an recomendado me colocado en esas lamparas que van aumentando la intensidad y nada me a funcionado deseo recibir información que de pronto si me sirva
Please forgive my replying in English, Rodrigo, but I trust that google translate will do the job!
I suspect that the reason phototherapy didn’t work for you is that it only treats the surface of the skin. It does not help the internal causes of vitiligo.
Rather than trying to tell you everything here, I will email you with a complete summary of what I did to recover my skin colour. Then you will have my email address so please feel free to ask any other questions that you may have after that.
Thanks for yet another highly interesting blog post, Caroline. One can only hope that if – sorry, when! – the closing of that core pathway were to happen, it would also send a message to our immune system, ‘hey, time to stop messing with your own cells and become balanced.’ And if the system then calmed down, well, that would be a consummation devoutly to be wished …
Kind regards,
Gösta
I am very much interested in what you did to fully repigmemt. I developed Vitiliago later in life although I may have had it for awhile but the pigment loss was in areas I was not even aware of. I have not come to terms with this nor accept what is happening to my skin/appearance. I do xtrac twice weekly and take supplements and have seen some but very little repigmemt. Any advise you can pass along will be greatly appreciated.
Sorry for the slow response, Ann – I have been away and it is taking a while to catch up with everything 🙂
From what I know about laser UVB treatment, it can be very effective in bringing about re-pigmentation but I believe the only way to get faster and more permanent results from any kind of light therapy is to also supplement with the nutrients that are needed for the pigmentation process. That is what I did and it is the only therapy that has ever worked for me.
I have dedicated a page on my site to summarising everything I did to reverse my vitiligo, so I hope this will be helpful. You can find it here:
https://thevitpro.com/treatment-summary.html
Good luck with your ongoing treatment!