Elder G H, Sheppard D M, Tovey J A, Urquhart A J
Lancet. 1983 Jun 11;1(8337):1301-4. doi: 10.1016/s0140-6736(83)92414-5.
Immunoreactive uroporphyrinogen decarboxylase was measured by rocket immuno-electrophoresis in haemolysates from 7 unrelated patients with familial porphyria cutanea tarda (PCT), 6 patients with sporadic PCT, and 7 normal subjects. In all patients with familial PCT immunoreactive enzyme protein was decreased (51% of normal), to the same extent as catalytic activity (56% of normal), whereas in sporadic PCT both measurements were normal. These results show that familial PCT is commonly caused by a mutation which does not lead to the production of non-catalytic cross-reactive immunological material. Familial PCT can be distinguished from other types of PCT by a simple immunoelectrophoretic method that does not involve measurement of uroporphyrinogen decarboxylase activity and which is therefore likely to be suitable for routine diagnostic use.
采用火箭免疫电泳法测定了7例无亲缘关系的家族性迟发性皮肤卟啉病(PCT)患者、6例散发性PCT患者和7名正常受试者溶血产物中的免疫反应性尿卟啉原脱羧酶。在所有家族性PCT患者中,免疫反应性酶蛋白降低(为正常的51%),与催化活性降低程度相同(为正常的56%),而散发性PCT患者这两项测定结果均正常。这些结果表明,家族性PCT通常由一种突变引起,该突变不会导致产生无催化活性的交叉反应性免疫物质。家族性PCT可通过一种简单的免疫电泳方法与其他类型的PCT相区分,该方法不涉及尿卟啉原脱羧酶活性的测定,因此可能适用于常规诊断。