Sullivan D A, Vaerman J P, Soo C
Department of Ophthalmology, Harvard Medical School, Boston, Massachusetts.
Immunology. 1993 Feb;78(2):308-17.
The objective of the present study was to examine and to compare the impact of severe protein malnutrition during development, adulthood and ageing on secretory immune expression in the eye, mouth and small intestine. In addition, we sought to determine whether potential abrogation of mucosal immunity by protein deprivation might be reversed by the administration of a balanced diet. Weanling, adult and aged rats were provided isocaloric diets containing 24% (control), 19%, 14%, 10%, 6% and/or 3.2% protein levels for defined periods and various immunological parameters were evaluated before, during and after the dietary regimen. Our results demonstrated the following. (1) Severe protein malnutrition (3.2%) dramatically suppressed the secretory immune system in eyes of weanling rats. After 8 weeks of protein insufficiency, tear IgA concentrations in young rats had undergone a precipitous decrease, such that IgA could not be detected in tears. This response was paralleled by a significant decline in the tear volume, tear secretory component (SC), IgG and total protein content, number of IgA-containing cells in lacrimal tissue, as well as the amounts of SC and/or IgA in saliva, intestinal secretions and serum. In contrast, the immunological effects of protein malnutrition in adult or aged animals varied considerably depending upon the specific mucosal site. (2) The influence of protein deprivation was dose dependent and reversible: maintenance of weanling rats on 10%, 6% or 3.2% protein diets interfered with the establishment of ocular and intestinal mucosal immunity, but later administration of optimal diets to these malnourished animals permitted a rapid immune recovery. (3) The impact of protein malnutrition on tear IgA levels in weanling animals, as shown by pair-feeding experiments, appeared to reflect primarily protein deficiency and not caloric restriction. Overall, these findings show that dietary protein plays a significant, site-specific role in the developmental expression of the secretory immune system.
本研究的目的是检测并比较发育、成年和衰老阶段严重蛋白质营养不良对眼、口腔和小肠分泌性免疫表达的影响。此外,我们试图确定蛋白质缺乏导致的黏膜免疫潜在缺失是否可通过给予均衡饮食得以逆转。给断奶、成年和老年大鼠在特定时期提供含有24%(对照)、19%、14%、10%、6%和/或3.2%蛋白质水平的等热量饮食,并在饮食方案实施前、期间和之后评估各种免疫参数。我们的结果表明如下几点。(1)严重蛋白质营养不良(3.2%)显著抑制了断奶大鼠眼部的分泌性免疫系统。蛋白质不足8周后,幼鼠泪液中IgA浓度急剧下降,以至于泪液中检测不到IgA。这种反应伴随着泪液量、泪液分泌成分(SC)、IgG和总蛋白含量、泪腺组织中含IgA细胞数量以及唾液、肠道分泌物和血清中SC和/或IgA量的显著下降。相比之下,成年或老年动物中蛋白质营养不良的免疫效应因特定黏膜部位的不同而有很大差异。(2)蛋白质缺乏的影响具有剂量依赖性且是可逆的:将断奶大鼠维持在10%、6%或3.2%蛋白质饮食会干扰眼和肠道黏膜免疫的建立,但随后给这些营养不良的动物喂食最佳饮食可使其免疫迅速恢复。(3)如配对喂养实验所示,蛋白质营养不良对断奶动物泪液IgA水平的影响似乎主要反映蛋白质缺乏而非热量限制。总体而言,这些发现表明饮食蛋白质在分泌性免疫系统的发育表达中发挥着重要的、部位特异性的作用。