Vitiligo and Acne Vulgaris Clinical Trial
Official title:
Cutaneous JAK Expression in Vitiligo and Acne Vulgaris.
The Janus kinase/signal transducer and activator of transcription (JAK-STAT) cytokine
signaling pathway is an emerging area of interest in dermatology, and emerging evidence
suggests that this pathway may play a crucial role in pathogenesis of inflammatory skin
disorders.
Recent advances on the role of cytokines in the pathophysiology of immune mediated
inflammatory diseases lead to the understanding that many pro inflammatory interleukins use
JAK/STAT components for signal transduction .
The JAK/STAT signaling pathway transmits information from extracellular chemical signals to
the nucleus resulting in DNA transcription. Binding of ligands, such as interferon and
interleukins, to their specific transmembrane receptors activate associated JAKs.
Phosphorylation of STAT follows, and the phosphorylated STAT translocates to the cell
nucleus and activates transcription or suppression of target genes .
The JAK family of non-receptor intracellular tyrosine kinases is comprised of four members,
JAK1, JAK2, JAK3 and tyrosine kinase (TyK)2. The JAKs are selectively activated by different
receptors and have, therefore, distinct in vivo roles. JAK1 is mainly activated by type II
cytokine receptors. JAK2 is crucial in transducing signals for cytokine receptors involved
in hematopoiesis (erythropoietin, thrombopoietin and haematopoietic cell development
cytokines). JAK3 is mainly expressed in B and T lymphocytes, and TYK2 associates commonly
with other JAKs.
Cutaneous JAK overexpression has already been demonstrated in a number of inflammatory skin
diseases (ISDs) including psoriasis, lichen planus (LP), atopic dermatitis (AD), pyoderma
gangrenosum (PG) and alopecia areata (AA); indicating its crucial role in inflammatory
keratinocytes.
Furthermore, the recent discovery of the JAK/STAT signaling pathway opened a new window of
opportunity for the treatment of ISDs and promoted the development of drugs that block JAK
activation.
JAK inhibitors in oral and topical formulations have shown beneficial results in psoriasis
and alopecia areata. Patients suffering from vitiligo might also benefit from JAK
inhibition. Recently, significant repigmentation was reported in a patient with vitiligo
after treatment with tofacitinib, an oral JAK 1/3 inhibitor . However, the knowledge of the
cutaneous JAK involvement in vitiligo is scarce. Similarly, little is known about cutaneous
JAK expression in acne vulgaris.
Considering the previous findings, there is a need for further elucidation of the JAK
signaling in other skin diseases as vitiligo and acne vulgaris.
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