Alopecia Areata Clinical Trial
Official title:
A Double-Blind, Placebo-Controlled, Randomized, Multi-Center Study to Evaluate The Safety and Therapeutic Efficacy of Intramuscular Administration of Alefacept in Patients With Chronic, Severe Scalp Alopecia Areata
The purpose of this study is to examine prospectively the safety and efficacy of alefacept in the treatment of subjects with severe alopecia areata of the scalp. Common features between psoriasis and alopecia areata, including immunologic and therapeutic aspects, suggest that alefacept, which has been shown to be a safe and statistically significant beneficial therapeutic modality for the treatment of psoriasis, may have therapeutic value in alopecia areata.
Alopecia areata (AA) is an autoimmune condition characterised by a T-cell mediated attack on
the hair follicle. The inciting antigenic stimulus is unknown. A dense peribulbar lymphocytic
infiltrate and reproducible immunologic abnormalities are hallmark features of the condition.
The cellular infiltrate primarily consists of activated T-lymphocytes and antigen-presenting
Langerhans cells. T-lymphocytes play a critical role in the pathogenesis of disease. The
observance of hair regrowth in those with alopecia areata who are treated with cyclosporine,
a known inhibitor of T-cell function, further confirms the central role of the T-lymphocytes
in the development of the disease.
Activation of T-cells is initiated by interaction of the T-cell receptor with the
antigen/major histocompatibility complex on the antigen-presenting cells. Co-stimulatory
interactions occur secondarily, including binding of the T-cell CD2 receptor to the
antigen-presenting cell ligand LFA-3 (lymphocyte function-associated antigen-3 CD58).
Induction of a molecular signaling cascade with resultant T-cell activation and proliferation
ensues. Abrogation of this activation may result in diminished or aborted expression of
disease, and thus suggests a potential therapeutic role for alefacept in the treatment of
alopecia areata. Alefacept is a bioengineered LFA-3/Immunoglobulin fusion protein that binds
to the CD2 T-cell receptor and interferes with the ligation of LFA-3. Binding of the
immunoglobulin portion of the fusion protein to the FCy receptor on antigen-presenting cells
potentiates apoptosis of CD-2 T-cells to thereby reduce the population of activated T-cells.
Psoriasis is a T-cell mediated disorder that shares many immunologic features with alopecia
areata. Accordingly, treatments that are effective in psoriasis often prove to be beneficial
in alopecia areata. Anthralin, topical and intralesional steroids and cyclosporine are among
several therapeutic agents that have efficacy in both disorders. Based on the impressive
therapeutic responses seen in those with psoriasis treated with alefacept, a similarly
beneficial outcome is tentatively anticipated with treatment of those with alopecia areata.
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