Mocchegiani E, Provinciali M, Di Stefano G, Nobilini A, Caramia G, Santarelli L, Tibaldi A, Fabris N
Gerontology Research Department, Italian National Research Centers on Aging (I.N.R.C.A.), Ancona.
Clin Immunol Immunopathol. 1995 Jun;75(3):214-24. doi: 10.1006/clin.1995.1074.
An altered cellular immune response as a secondary phenomenon has been suggested to be probably involved in the bronchopulmonary infections by Pseudomonas aeruginosa in cystic fibrosis (CF). The difficulty to eradicate with modern anti-pseudomonal antibiotics the bronchopulmonary infections has led us to further investigate the possible existence of other cellular immune defects and their cause. Alterations in zinc turnover are present in CF. Zinc is relevant for good immune functioning. In particular, zinc is required to confer biological activity to thymulin (ZnFTS), a biochemically defined thymic hormone with a modulating action on cell-mediated immunity. The zinc-unbound form (FTS) is inactive and it can be unmasked by in vitro zinc addition to the plasma samples revealing the total amount of circulating thymulin (active + inactive). Marginal zinc deficiencies may prevent peripheral biological activation of active thymulin. Total zinc-saturable thymulin fractions in CF are similar to those observed in normal subjects, whereas the active quota is strongly reduced associated with concomitant high plasma levels of inactive thymulin compared to the values of healthy children (P < 0.01). A strict correlation exists between zinc and thymic hormone-saturable fraction (r = 0.87, P < 0.01) in CF. These findings suggest that the defect is not due to a thymic failure but to a reduced peripheral saturation of thymulin by zinc ions. This defect might depend on augmented plasma concentration of alpha 2-macroglobulin, which has a higher binding affinity for zinc than thymulin. T cell subsets are normal in CF. Reduced NK cell number and activity are present. Also, plasma IL-2 levels are reduced. The existence of positive correlations between zinc and IL-2 (r = 0.79, P < 0.01) and between zinc or active thymulin and NK activity (r = 0.70, P < 0.01 and r = 0.88, P < 0.01, respectively) suggest a close link among zinc failure, impaired IL-2 activity, low thymulin level, and reduced NK activity in CF patients with both normal and growth retardation. Although the role of NK cells is unknown in CF, a zinc supplementation, in order to induce a complete saturation of thymulin molecules, to correct some cellular immune defects and to improve the growth, may be suggested.
细胞免疫反应改变作为一种继发现象,被认为可能与囊性纤维化(CF)患者铜绿假单胞菌引起的支气管肺部感染有关。现代抗假单胞菌抗生素难以根除支气管肺部感染,这促使我们进一步研究是否存在其他细胞免疫缺陷及其原因。CF患者存在锌代谢异常。锌对良好的免疫功能至关重要。特别是,锌是赋予胸腺素(ZnFTS)生物活性所必需的,胸腺素是一种生化定义的胸腺激素,对细胞介导的免疫有调节作用。未结合锌的形式(FTS)无活性,可通过在血浆样本中体外添加锌来揭示循环胸腺素的总量(活性+非活性),从而使其显现出来。边缘性锌缺乏可能会阻止活性胸腺素的外周生物激活。CF患者中总锌可饱和胸腺素组分与正常受试者相似,然而与健康儿童相比,活性份额显著降低,同时非活性胸腺素的血浆水平较高(P<0.01)。CF患者中锌与胸腺激素可饱和组分之间存在严格的相关性(r = 0.87,P<0.01)。这些发现表明,缺陷并非由于胸腺功能衰竭,而是由于锌离子对胸腺素的外周饱和度降低。这种缺陷可能取决于α2-巨球蛋白血浆浓度的增加,α2-巨球蛋白对锌的结合亲和力高于胸腺素。CF患者的T细胞亚群正常。NK细胞数量和活性降低。此外,血浆IL-2水平降低。锌与IL-2之间(r = 0.79,P<0.01)以及锌或活性胸腺素与NK活性之间(分别为r = 0.70,P<0.01和r = 0.88,P<0.01)存在正相关,这表明在生长正常和生长迟缓的CF患者中,锌缺乏、IL-2活性受损、胸腺素水平低和NK活性降低之间存在密切联系。尽管NK细胞在CF中的作用尚不清楚,但为了使胸腺素分子完全饱和、纠正一些细胞免疫缺陷并促进生长,可能建议补充锌。