Brown M D, Gupta A K, Ellis C N, Rocher L L, Voorhees J J
Department of Dermatology, University of Michigan Medical Center, Ann Arbor.
Adv Dermatol. 1989;4:3-27; discussion 28.
Cyclosporin A is a potent immunosuppressive drug with almost a decade of clinical use. Due to its lack of bone marrow toxicity, it has assumed a leading role in organ transplant surgery. Likewise, it has shown remarkable efficacy in psoriasis and has shown potential usefulness in other dermatologic diseases, most of which are thought to have an autoimmune T-cell-mediated pathogenesis. There are many other inflammatory skin conditions in which T lymphocytes represent a majority of the cellular infiltrates, and theoretically such disorders may be responsive to CsA. Diseases such as lichen planus, allergic contact dermatitis, photoallergy, and vitiligo are potential areas of further study. The potential use of topical and intralesional CsA also warrants further clinical evaluation. There are reports of topical CsA showing effectiveness for alopecia areata and nickel contact sensitivity. Griffiths et al. treated six psoriatic patients with 2% CsA ointment twice daily for 4 weeks. The response to placebo or CsA at the end of the study was similar in all patients. Notably, there was no measured systemic absorption and no change in blood pressure or renal function. We had similar unimpressive results in several patients treated with a 10% solution of CsA; minimal to no response was seen. Of great benefit would be an effective topical preparation without systemic absorption or toxicity. Future studies will need to carefully evaluate the vehicle used and the strength of topical CsA employed. The role of CsA in dermatologic disease still needs much investigation, both at the clinical and basic science levels. The studies to date show dramatic and exciting results. Indeed, CsA may well represent a major advance in the understanding and treatment of psoriasis. However, the decision to use CsA for nonfatal diseases such as psoriasis will require a careful balance between efficacy and toxicity. If long-term side effects can be avoided or kept within reasonably safe, acceptable limits, CsA holds great promise for the treatment of psoriasis. It may at times be used as an acute intervention, with a relatively large, initial dose for a short period of time to quickly clear severe psoriasis. This could be followed by either a reduction to a lower and safer maintenance dose or a program of other treatments. Cyclosporin A may also prove useful alone in very low doses or in combination therapy, as with UVB or PUVA. Optimal dosing protocols are currently under investigation.
环孢素A是一种强效免疫抑制药物,已临床应用近十年。由于其缺乏骨髓毒性,它在器官移植手术中发挥了主导作用。同样,它在银屑病治疗中显示出显著疗效,并且在其他皮肤病中也显示出潜在的应用价值,其中大多数皮肤病被认为具有自身免疫性T细胞介导的发病机制。还有许多其他炎症性皮肤病,其中T淋巴细胞是细胞浸润的主要成分,理论上这些疾病可能对环孢素A有反应。扁平苔藓、过敏性接触性皮炎、光过敏和白癜风等疾病是进一步研究的潜在领域。局部和皮损内注射环孢素A的潜在用途也值得进一步临床评估。有报道称局部使用环孢素A对斑秃和镍接触性敏感有效。格里菲思等人用2%环孢素A软膏每天两次治疗6例银屑病患者,持续4周。研究结束时,所有患者对安慰剂或环孢素A的反应相似。值得注意的是,未检测到全身吸收,血压和肾功能也无变化。我们用10%环孢素A溶液治疗的几名患者也得到了类似的不理想结果,几乎没有反应。一种没有全身吸收或毒性的有效局部制剂将非常有益。未来的研究需要仔细评估所使用的载体和局部环孢素A的浓度。环孢素A在皮肤病中的作用在临床和基础科学层面仍需大量研究。迄今为止的研究显示出显著且令人兴奋的结果。事实上,环孢素A很可能代表了银屑病认识和治疗方面的一项重大进展。然而,对于银屑病等非致命性疾病使用环孢素A的决定需要在疗效和毒性之间仔细权衡。如果能够避免长期副作用或将其控制在合理安全、可接受的范围内,环孢素A在银屑病治疗方面前景广阔。它有时可作为急性干预措施,短期内使用相对较大的初始剂量以快速清除重度银屑病。随后可将剂量降至较低且更安全的维持剂量或采用其他治疗方案。环孢素A单独使用极低剂量或与UVB或PUVA联合治疗可能也会证明有用。目前正在研究最佳给药方案。