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在动物模型中牛奶及以牛奶为基础的配方奶粉的相对变应原性。

Relative allergenicity of cow's milk and cow's milk-based formulas in an animal model.

作者信息

Kitagawa S, Zhang S, Harari Y, Castro G A

机构信息

Department of Pediatrics, University of Texas Medical Branch, Galveston, USA.

出版信息

Am J Med Sci. 1995 Nov;310(5):183-7. doi: 10.1097/00000441-199511000-00002.

DOI:10.1097/00000441-199511000-00002
PMID:7485221
Abstract

Human infants fed cow's milk or cow's milk-based formula may become intolerant to milk proteins partially because of allergic reactions. However, the relative allergenicity of these diets has not been clearly determined at the intestinal level. In this study, the allergenicity of cow's milk and milk-based formula was evaluated by examining intestinal anaphylaxis caused by challenge with a milk protein fraction, beta-lactoglobulin (beta LG), in guinea pigs orally sensitized to these diets. Colonic segments were removed and challenged with beta LG. An antigen-induced, anaphylactically mediated elevation of transmural short circuit current, which is caused by net chloride (Cl-) secretion, was measured in Ussing chambers as an index of local immune responsiveness. After removal of the colon, all guinea pigs were challenged by intracardiac injection with beta LG to examine the onset of bronchospasm, a test for systemic anaphylaxis. Whereas colonic segments from all guinea pigs fed whole cow's milk responded to challenge with beta LG, segments from only 60% of animals fed cow's milk formula responded to the challenge. In addition, the responders in the latter group had a significantly lower magnitude of beta LG-induced Cl- secretion compared with animals sensitized to whole cow's milk. In parallel, bronchospasm developed in all guinea pigs fed whole cow's milk. In the group of animals fed cow's milk formula, bronchospasm developed only in those who responded to the intestinal challenge. On the basis of these results, cow's milk-based formula has less sensitizing power than whole cow's milk in our animal model, and our approach is effective in testing allergenicity at the intestinal level.

摘要

食用牛奶或基于牛奶的配方奶粉的人类婴儿可能会对牛奶蛋白产生不耐受,部分原因是过敏反应。然而,这些饮食在肠道水平上的相对致敏性尚未明确确定。在本研究中,通过检测对这些饮食进行口服致敏的豚鼠在受到牛奶蛋白组分β-乳球蛋白(β-LG)激发后引起的肠道过敏反应,评估了牛奶和基于牛奶的配方奶粉的致敏性。切除结肠段并用β-LG进行激发。在尤斯灌流小室中测量由净氯化物(Cl-)分泌引起的抗原诱导的、过敏介导的跨膜短路电流升高,作为局部免疫反应性的指标。切除结肠后,所有豚鼠通过心内注射β-LG进行激发,以检查支气管痉挛的发作情况,这是一种全身性过敏反应的测试。虽然所有喂食全脂牛奶的豚鼠的结肠段对β-LG激发有反应,但只有60%喂食牛奶配方奶粉的动物的结肠段对激发有反应。此外,与对全脂牛奶致敏的动物相比,后一组中的反应者β-LG诱导的Cl-分泌幅度明显较低。同时,所有喂食全脂牛奶的豚鼠均出现支气管痉挛。在喂食牛奶配方奶粉的动物组中,支气管痉挛仅在那些对肠道激发有反应的动物中出现。基于这些结果,在我们的动物模型中,基于牛奶的配方奶粉的致敏能力低于全脂牛奶,并且我们的方法在测试肠道水平的致敏性方面是有效的。

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