Nielsen H J
Department of Surgical Gastroenterology, Hvidovre Hospital, Copenhagen.
Dan Med Bull. 1991 Dec;38(6):478-80.
The findings that the immunosuppressant cyclosporine A (CsA) improves psoriasis raise the possibility that cellular immune processes may play a major role in the pathogenesis of this disease. It is broadly agreed that histamine released by mast cells is one of the molecules involved in the pathogenesis. This is supported by the findings that CsA and methotrexate (Mxt) reduce formation and release of histamine. However, the well known side-effects of CsA and Mxt may argue potential use of other agents acting on formation and action of histamine. Such agents may be the histamine-2 receptor antagonists, previously reported to have a clinical effect on psoriasis. But randomised short-term studies have disclosed that these drugs have no beneficial or even an aggravating effect on the disease. This article reports on recent findings of improvement in psoriasis using high doses of the histamine-2 receptor antagonist ranitidine in long-term studies. Also presented are a hypothetical action of histamine in development of psoriasis and a rationale for ranitidine as a potential agent in the therapy of psoriasis.
免疫抑制剂环孢素A(CsA)可改善银屑病,这一发现提示细胞免疫过程可能在该疾病的发病机制中起主要作用。人们普遍认为,肥大细胞释放的组胺是参与发病机制的分子之一。环孢素A和甲氨蝶呤(Mxt)可减少组胺的形成和释放,这一发现支持了上述观点。然而,环孢素A和甲氨蝶呤众所周知的副作用可能表明有必要使用其他作用于组胺形成和作用的药物。这类药物可能是组胺-2受体拮抗剂,此前有报道称其对银屑病有临床疗效。但随机短期研究表明,这些药物对该疾病并无益处,甚至有加重作用。本文报道了在长期研究中使用高剂量组胺-2受体拮抗剂雷尼替丁改善银屑病的最新发现。文中还提出了组胺在银屑病发病过程中的假设作用,以及雷尼替丁作为银屑病潜在治疗药物的理论依据。