New and Experimental Treatments of Vitiligo
Torello Lotti, MD, Francesca Prignano, MD,
Department of Dermatological Sciences, University of Florence, Via Lorenzo il Magnifico, 104, 50129, Florence, Italy
cutaneous hypopigmentation, and this article is
In recent years, the interest in vitiligo, among
dedicated to the introduction of and discussion
all the other hypopigmentation disorders, is in-
about the most recent and innovative researches
creasing, partly because of the aesthetic challenge
in the treatment of vitiligo and other depigment-
represented by the disease itself and partly as a
ing disorders. It also provides a description of the
reaction to the intolerable discrimination against
newly developed techniques that are in the hands
the affected subjects. Vitiligo is not an unmanage-
of dermatologists, dermato-cosmetologists, and
able disease, and many studies on new therapeutic
protocols showed a relevant efficacy, even if we
We cannot ignore the fact that among all the
are far from the ultimate therapy This interest
hypomelanoses, vitiligo is the most remarkable
in vitiligo has the effect of discovering alternative
and challenging and that almost all the research
and, in some cases, more efficient treatment mo-
and innovations made in the field of hypopigmen-
dalities to be used in other primitive or secondary
tation treatment are caused by the continuous
hypomelanoses, such as piebaldism, pityriasis alba,
efforts to reach the ultimate therapy for vitiligo.
posttraumatic and postinfectious hypopigmenta-
We must be fully aware that not all hypopigmen-
tation disorders respond in the same way to the
different treatment modalities. Several hypomela-
noses are reversible and do not require any
resetting completely the appearance and function
treatment. In contrast, therapy of permanent
of the healthy skin. Melanocytes usually respond
hypomelanoses is difficult and often unsuccessful.
slowly to the different treatments, so it could take
Multiple treatment options are available for de-
several months to reach acceptable results in term
pigmentation caused by vitiligo, whereas the treat-
of repigmentation. Affected subjects must be
ment of leukoderma in disorders such as nevus
aware of this process and acquiesce with the
depigmentosus, hypomelanosis of Ito, tuberous
possibility of a long-term therapy. Newly avail-
sclerosis, and piebaldism is limited. Because of
able treatments for hypopigmentation are medi-
their inflammatory etiology, postinflammatory
cal, physical, and surgical, alone or in association
hypopigmentations may be well treated with clas-
sical approaches (eg, topical corticosteroids andphototherapy). Conversely, disorders such as ocu-
locutaneous albinism are not currently capable ofundergoing repigmentation therapy.
stimulated by UV light in terms of effectiverepigmentation must be confirmed, the efficacyof UVB light in vitiligo is probably caused by the
production of high levels of cis-urocanic acid,
a metabolic product that causes cutaneous
0733-8635/07/$ - see front matter Ó 2007 Elsevier Inc. All rights reserved. doi:10.1016/j.det.2007.04.009
are related to less erythema, no phototoxic effects,
and no epidermal thickening after long-term irra-
diation. No statistical differences exist betweenPUVA, NB-UVB, or broadband UVB regarding
UVB narrow band microphototherapyUVB narrow band excimer laser and
Ultraviolet B narrow band microphototherapy
This new therapeutic approach evolved from
the consideration that vitiligo patients undergoing
phototherapy were receiving a high cumulative
dose of radiation during their lives, which led to
secondary cutaneous disorders, such as photo-
aging, telangiectasias, and excessive tanning.
These considerations led to the development of
which involved so-called ‘‘microphototherapy’’. Microphototherapy is based on a photo expo-sition limited to well-defined areas, and it avoids
immune suppression. Melanogenesis is thought to
the collateral effects associated with diffuse photo-
be stimulated by UVB radiation through the
therapy (eg, photoaging, erythema, and burns)
activation of nitric oxide-cGMP-proteinkinase G
pathway, and/or by the activation of the cAMP-
TL-10) with a wavelength peak at 311 nm that is
pathway by alpha-melanotropin, and/or through
selectively delivered to the white patches. It en-
melanocyte-stimulating hormone receptor-bind-
ables drastic reduction of the total dose of radia-
ing activity and melanocortin receptor gene ex-
tion and the most common side effects related to
the exposition to UV rays: excessive tanning of
The first data on the use of UVB in the treatment
the nonaffected skin, photoaging, telangiectases,
of vitiligo (broadband UVB: 280–320 nm) ap-
and the risk of neoplasms. It also avoids an
peared in 1990, whereas the first report on UVB
increase in the chromatic contrast between normal
narrow band (NB-UVB) therapy (NB-UVB: 311
and lesional skin. With this treatment, one can
Æ 2 nm) appeared in 1997 This latter study
administer different doses of UVB radiation in
showed that NB-UVB were more effective, com-
different areas of the body (ie, the hands need
pared with topical UVA treatment, in the treat-
more UVB than the eyelids to repigment), which
ment of vitiligo, with faster repigmentation and
optimizes the treatment by tailoring it to each
less contrast between normal and depigmented
skin . Subsequent meta-analysis on nonsurgical
The initial dose of radiation is 20% less than
treatments for vitiligo showed that results obtained
the minimum erythema dose, which is evaluated
with UVB and NB-UVB therapy were almost the
through the exposition of affected and unaffected
same as results obtained with psoralen plus Ultra
skin to increasing doses of UVB (80, 160, 240,
Violet A (PUVA) . A combination of UVB and
320, 400 mW/cm2) at least 3 days before the be-
other therapies, such as pseudocatalase, calcipo-
ginning of the treatment. During the following
triol, and phenylalanine, was considered.
sessions, each patch is uniformly irradiated. In
Treatment protocols vary in different studies,
‘‘sensitive’’ areas (eg, eyelids), 80% of minimum
with an initial dose of irradiation ranging from
erythema doses are used. The radiation dose is
0.075 J/cm2 to 0.25 J/cm2 and increasing by 20%
increased by 20% at each session. When erythema
after each treatment until a slight erythema is
occurs, the dose is lowered by 20% in the ery-
reached. Cumulative doses are lower than in
thematous area only. Some skin areas can resist
PUVA therapy, however. Stating the major ad-
photostimulation better and are irradiated with
vantages of avoiding psoralen side effects and
higher regimens (up to twice the dose of the
low cumulative dose of radiation, evidence-based
most sensitive areas). Sessions are repeated every
guidelines for the treatment of vitiligo indicate
21 to 30 days until repigmentation is reached,
that NB-UVB phototherapy is recommended for
generalized vitiligo UVB treatments can be
Partial repigmentation is often seen after at
safely used in pregnant women and children and
least three to six sessions (63% of the cases),
beginning just after 2 months of treatment as
treatment duration (ranging from 17–57 months
a pigment pitting around each follicular ostium
of therapy in this study) and lower mean duration
(follicular repigmentation) usually accompanied
by an evident interfollicular repigmentation. Pho-
This technique, which is among the newest
tographic evaluation is useful to assess the clinical
ones, should deserve further attention, and
results, and Wood’s light is used for lighter
perhaps focus on the treatment of other diseases
that occur with hypomelanosis. Similarly, mono-
In a recent study, 734 patients were irradiated
chromatic excimer light has shown similar positive
using this protocol every 2 weeks for 12 consec-
effects in the repigmentation of vitiligo patches
utive months At the end of the study period,
69.8% of patients (n ¼ 510) achieved normal pig-mentation on more than 75% of the treated areas,
21.12% (n ¼ 155) achieved 50% to 75% repig-mentation on the treated areas, and only 9.4%
Low levels of catalase in the epidermis of
(n ¼ 69) showed less than 50% repigmentation
patients who have vitiligo increase H2O2 levels,
with no statistical significance between segmental
which inhibits 6-BH4 metabolism and melanogen-
and nonsegmental vitiligo. (In 5 patients in this
esis . The use of creams containing pseudo-
group the vitiligo was aggravated.) The results
of this study are similar to those obtained by to-
progression and induce repigmentation . Pseu-
tal-body UVB irradiation in international studies,
docatalase acts as a substitute for impaired levels
enriched by the advantages of fewer side effects.
of catalase, degrading excessive hydrogen perox-
Microphototherapy is particularly useful in
ide and allowing recovery of enzyme activities.
patients affected by segmental vitiligo and bi-
Narrow band UVB-activated topical pseudocata-
lateral symmetrical vitiligo in whom the total
lase has been proposed for vitiligo treatment,
amount of body surface involved is less than
but although some repigmentation has been ob-
20%. The only side effect occasionally reported
served in approximately 60% of patients treated
is transient erythema, rarely followed by desqua-
with this modality, the degree of contribution of
the UVB radiation to these results is not known
tered to patients who have actinic sensitivity (eg,
systemic lupus erythematosus, xeroderma pigmen-
Some authors report positive results after
tosum, porphyriasis, cutaneous viral infections) or
topical administration of tacrolimus ointment
patients treated with topical or systemic photosen-
0.1%, particularly on sun-exposed areas of the
skin (eg, face and neck) Tacrolimus seemsto work selectively by inhibiting T-lymphocyteactivation, which blocks the production and
secretion of proinflammatory cytokines, such as
tumor necrosis factor-a, whose levels are in-
After the consistent results obtained by narrow
creased in vitiligo skin but not in healthy controls
band microphototherapy with light source devices
. This finding suggests that repigmentation
such as BIOSKIN, another innovationdstill ex-
could be partly associated with reduced levels of
perimentaldwas introduced: excimer laser ther-
tumor necrosis factor-a in affected skin. The asso-
apy and monochromatic excimer light therapy
ciation of tacrolimus ointment with excimer laser
with monochromatic UV rays at 308 nm. These
308 nm seems an effective treatment for vitiligo,
therapies are not so different from the ‘‘classical’’
but the possibility of unexpected sunburns must
narrow band radiation. They are capable of
selectively treating single hypopigmented patches
similarly active in the treatment of vitiligo
and sparing nonaffected areas. A recent study
analyzed the effects of excimer laser in 24 patients
A recent approach to the treatment of vitiligo
and reported total repigmentation in the treated
is based on the thought that UV ray–induced
areas in 12% of subjects (n ¼ 7), partial (25%–
melanogenesis is partly caused by UV-induced
75%) repigmentation in 25% (n ¼ 6), less than
turnover of membrane phospholipids that gener-
25% repigmentation in 25% of patients, and no
ate prostaglandins and other products, maybe
results in 20.8% of patients (n ¼ 5) The
representing the activating signal for repigmenta-
efficacy of the treatment seems to be related to
tion. Some authors observed in vitro enhancement
of melanogenesis by PGE2, and in a recent study
responsive to medical treatment and in patients
vitiligo patients with less than 5% skin involve-
who have piebaldism or persistent depigmentation
ment were treated with a topical a gel that con-
caused by halo nevi, thermal burns, trauma, or
tained 166.6 mg/g PGE2 applied in the evening
inflammation. Surgical options are considered for
patients who have vitiligo with areas of involve-
24 patients evaluated at the end of the study pe-
ment more than 2 to 3 cm that contain depig-
riod, 15 reported marked (50%–75%) to complete
mented hairs or involvement of sites such as the
repigmentation (6 focal vitiligo, 7 vitiligo vulgaris,
lips or fingers, which are unlikely to have a satis-
2 segmental vitiligo), whereas 6 patients showed
factory response to medical therapy. It is manda-
25% to 50% improvement and 6 showed minimal
tory that the disease be stable; stability is the most
or no improvement. The observed side effects were
critical factor in the selection of patients with
episodes of mild irritation after exposure to sun-
recalcitrant vitiligo as candidates for surgical
light. Although the exact mechanism of repigmen-
repigmentation. Some authors suggest surgically
tation is not clear, different mechanisms have been
treating vitiligo patches only if stable for at least 2
suggested, including (1) influencing melanocyte
years and performing a minigrafting test before
responsiveness to neuronal stimulation, (2) mela-
the graft to evaluate the positive response and the
nocyte proliferation, and (3) direct or second mes-
absence of koebnerization at the donor site after 2
senger-mediated interaction with melanocytes
to 3 months follow-up Active vitiligo has
through the stimulation of tyrosinase activity.
a higher risk for graft failure, recurrence of depig-
Other mechanisms that do not directly involve
mentation, and koebnerization at the donor site
melanocytes have been proposed, but one of the
. Other important factors that affect graft out-
most interesting focuses on the immunosuppres-
come in patients who have vitiligo include the lo-
sive role of in vitro and in vivo PGE2 . Other
cation and type of disease, with 95% success rates
trials should be undertaken to evaluate the correct
for test grafting in segmental or focal vitiligo ver-
use of topical prostaglandin analogs in patients
sus 50% or less in generalized vitiligo A re-
cent review on this argument showed that better
Patients who have vitiligo exhibit reduced
surgical results can be obtained in segmental viti-
levels of intracellular calcium in keratinocytes and
ligo and in patients younger than age 20
melanocytes The calcium decrease parallels
Because of the multiple, time-intensive pro-
increased thioredoxin levels, which could inhibit
cedures involved in autologous transplantation,
tyrosinase activity and melanogenesis. Derivatives
these techniques are best suited for repigmenta-
of vitamin D act on melanocyte receptors for 1,25-
tion of limited areas of leukoderma, with priority
dihidroxy-vitamin D, modifying the altered calcium
given to exposed sites. They are reserved for
homeostasis and permitting a more rapid repigmen-
adolescents and adults who are firmly motivated.
tation when used alone and when associated with
Surgical therapies are not recommended for
patients with a tendency to form keloids or
Cucumis melo extracts have shown relevant su-
develop hyperpigmentation after minor trauma,
per-oxide-dismutase and catalase-like activities
and success has not been reported in disorders of
when associated with selective UVB therapy
hypopigmentation, such as nevus depigmentosus
In vitro and experimental data show an interesting
performance of this vegetable extract, which is
Techniques of surgical repigmentation involve
well accepted by patients who have vitiligo and
the transfer of melanocytes, melanocytes and
family members of children affected by the
keratinocytes, or full-thickness skin from normally
disease. Excellent results have been observed in
pigmented areas to hypomelanotic patches. Autol-
association with focused UVB narrow band (BIO-
ogous skin grafts can be divided into three major
SKIN) treatment, which shows that the associa-
groups: (1) grafting of normal skin (epidermis with
tion represents a safe and effective treatment and
or without dermis) that contains melanocytes, (2)
is well tolerated and accepted by patients
grafting of a noncultured epidermal or hair folliclesuspension that contains melanocytes, and (3)grafting of cultured melanocytes with or without
keratinocytes, in suspension or as sheets
The first group includes different techniques.
repigmentation in a subset of patients who have
The thin dermo-epidermal grafts technique in-
stable vitiligo that is refractory or partially
volves replacing the achromic lesions of vitiligo
with thin dermal and epidermal sheets that are
hair follicles and the epidermis. The cells are put
taken from the donor site with a dermatome at
into a suspension for direct application to the
a depth of 0.1 to 0.3 mm to avoid scarring.
recipient site without expansion by culture
Superficial dermabrasion is used to prepare the
This technique is relatively simpler and less time
receiving site to the graft. This method is success-
consuming than other methods (especially cell cul-
ful in up to 80% of treated patients, avoids
ture methods) and smaller areas can be treated,
scarring, and permits repeated grafts from donor
but rates of success are lower (30%–70%) .
sites . A possible variation is so-called ‘‘seed
Cultural methods can be applied to surgical
grafting,’’ in which a thin piece of epidermal
techniques. Cultured epidermis with melanocytes
skin graft is taken from the donor site with
with or without keratinocytes and cultured mela-
a hand dermatome and minced into fragments
nocytes with or without keratinocyte suspensions
smaller than 1 mm2. These pieces are placed on
can be applied to previously dermabrased re-
the epidermal-abraded vitiligo lesions and covered
cipient areas. The donor sites can be small, and
with a specific medication for 5 to 7 days. Photo-
the cells are seeded to stimulate melanocytes and
therapy can follow surgery to enhance results .
keratinocytes until many more cellsdor even
Suction-blister epidermal grafting using suction
a thin epidermal sheetdare obtained and placed
devices is another similar technique that is popu-
on recipient sites previously prepared with one of
lar and yields excellent results . Full-thickness
the various methods. With this technique, satis-
minigrafts (1–2 mm) have become one of the most
factory results are obtained even when treating up
common surgical methods to treat vitiligo. Multi-
to 30% of total body surface, with more than 75%
ple donor areas are harvested with a small punch
repigmentation rate in more than half of treated
(1–1.2 mm). Minigrafts are placed in the recipient
patients Small donor areas can be used to
areas, which are prepared depending on the graft
cover large hypopigmented areas (up to 500 times
type. The grafts range from the removal of
larger than the donor site). The achieved repig-
‘‘punches’’ similar to those harvested from the do-
mentation is relatively uniform, with only minimal
nor area to liquid nitrogen–induced blisters, derm-
textural changes. Cell cultures are more expensive
abrasion, or laser ablation (eg, Er:YAG laser) and
than other surgical methods, require specific labo-
are sealed with sterile adhesive medication. This
ratory facilities, and require a 2- to 5-week period
method allows repigmentation in 1 to 3 months
in 70% to 100% of cases by melanocytes spread-
Side effects of vitiligo surgery include Ko¨bner
phenomenon of the donor site, keloids, hyperpig-
monly located on the medial upper arms, thighs,
mentation, ‘‘cobblestoning,’’ scarring, and infec-
or buttocks (‘‘hidden’’ sites).
tion. Careful handling of the donor and recipient
Methodologic variations include flip-top trans-
plants, in which the epidermis at the recipient site
Treatment with tissue-engineered skin uses
is not removed but rather used to form multiple
biomaterials such as perforated membranes of
hinged flaps, each covering an ultrathin 1- to 2-
semi-synthetic biopolymers of hyaluronic acid
mm graft harvested from the donor site using
100% esterified with benzyl alcohol. Epidermal
a razor blade Single-hair grafting techniques
culture obtained from normally pigmented sites is
from donor sites on the scalp are particularly ef-
optimally delivered to the recipient achromatic
fective for treating hairy areas, such as the eyelids
patches previously de-epithelized by laser abla-
and eyebrows . Repigmentation of hairs in
tion. Excellent and lasting repigmentation without
areas of leukotrichia also has been observed
side effects has been reported . Surgical repig-
with this and other methods, which suggests a mi-
mentation techniques can be used with other
gration of melanocytes from the grafted epidermis
therapeutic protocols, such as BIOSKIN micro-
to the external root sheath of the hair follicle and
then to the hair bulb. Posttransplantation sunlight
. Cell culture techniques also can require
exposure for 10 to 15 minutes per day or photo-
the use of mitogens to enhance cell growth.
therapy can help stimulate melanogenesis
In transplants of noncultured keratinocyte/
melanocyte suspensions, donor tissue from a shavebiopsy of the buttocks or full-thickness biopsy of
In patients with extensive areas of depig-
the scalp is digested with trypsin anddin the latter
mentation or disfiguring lesions that do not res-
casedcollagenase to obtain melanocytes from the
pond to repigmentation therapies, therapeutic
depigmentation of the residual pigmented areas
Q-switched ruby laser, like chemical depigmenta-
of the skin should be considered. Patients should
tion, does not seem to kill follicular melanocytes.
be informed that therapeutically induced depig-
Cryotherapy has been used recently for de-
mentation is permanent and irreversible and that
pigmentation in patients who have vitiligo be-
they always will be at risk of suffering sunburns,
cause of its known melanotoxic capabilities
premature ageing, and cutaneous neoplasms. It is
In this study, five patients were treated with one
necessary to minimize sun exposure and apply
to three sessions of cryotherapy, and all of them
achieved complete depigmentation with no side
effects. After 8 months follow-up, two patients
proved the use of monobenzyl-ether of hydroqui-
showed partial lentigo-like repigmentation on sun-
none (MBEH) for depigmentation in patients who
exposed areas, which was retreated with cryother-
have vitiligo that involves more than 50% of their
apy or chemical peeling. Repigmentation is still
body surface area. People who suffer from a less
a problem, however, as is the case with all depig-
widespread vitiligo can benefit from depigmenta-
tion therapy, however, particularly because alter-native modalities have been developed. Recently,
the sequential use of 4-methoxyphenol and the
Alternative treatments include light exposure
have been reported as alternative options for de-
L-phenylalanine (oral or topical), khellin
(topical), melagenina I and II (topical), and topi-
pigmentation therapy, with promising results.
cal minoxidil treatment. Homeopathy, ayurvedic
medicine, and climatologic and balneologic thera-
or mequinol) is a phenol derivative with melano-
cytotoxic properties (similar to those of MBEH)that has been used in patients who have vitiligowith results comparable to those obtained by
to MBEH because in many European countries
treated successfully with medical, physical, and
the latter is no longer available, mainly because
surgical techniques with excellent results. Thera-
of its side effects. As for MBEH, the indication
peutic strategies are being developed to minimize
for using 4-methoxyphenol includes only depig-
the side effects of previous treatments and are
mentation in patients who have vitiligo.
used for children with vitiligo. To reach optimal
A recently developed depigmentation therapy
clinical results in terms of repigmentation and
for vitiligo is based on the use of Q-switched ruby
minimizing side effects, narrow band UVB–
laser, which has a wavelength of 694 nm and is
focused treatment represents the treatment of
capable of selectively destroying melanin and
choice when vitiligo affects less than 10% of the
melanin-containing structures of the skin
The risk of scarring is minimal, and depigmenta-tion is rapidly achieved (7–14 days) comparedwith bleaching agents (1 month–1 year). Pain
caused by the procedure can be managed easily
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Fachinformation des Arzneimittel-Kompendium der Schweiz® Wirkstoff: Esomeprazolum ut Natrii esomeprazolum. Hilfsstoffe: Natrii edetas, Natrii hydroxidum. Galenische Form und Wirkstoffmenge pro EinheitPulver zur Herstellung einer Injektions- oder Infusionslösung. Trockenampulle (Durchstechflasche) zu 42,5 mg Natrii esomeprazolum (äquivalent zu 40 mg Esomeprazol). Indikationen/Anwendungsmöglic