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通过热处理降低乳清蛋白的抗原性:生产低敏婴儿配方奶粉的一种可能策略。

Reduction in the antigenicity of whey proteins by heat treatment: a possible strategy for producing a hypoallergenic infant milk formula.

作者信息

Heppell L M, Cant A J, Kilshaw P J

出版信息

Br J Nutr. 1984 Jan;51(1):29-36. doi: 10.1079/bjn19840006.

Abstract

Residual antigenic protein in heat-denatured cow's milk whey and in two commercial infant milk formulas was determined using enzyme-linked immunosorbent assays specific for beta-lactoglobulin, alpha-lactalbumin, bovine serum albumin, bovine IgG1 and alpha-casein. This immunochemical assessment of antigenicity was related to the capacity of the preparations to sensitize immunologically when fed to guinea-pigs for 2 weeks. Antibody production was measured and the susceptibility of the animals to systemic anaphylaxis was assessed by injecting them intravenously with heated or unheated milk proteins. Whey protein that had been heated at 100 degrees or 115 degrees for 30 min was extensively denatured and, in contrast to pasteurized whey, failed to sensitize guinea-pigs for anaphylaxis. Antibody production was undetected or very low. The proteins in SMA powder and SMA Gold Cap liquid concentrate were less denatured and animals given these formulas prepared according to the maker's instructions produced relatively high levels of antibodies to beta-lactoglobulin and alpha-casein and a majority developed anaphylaxis when injected intravenously with these products. As well as failing to sensitize, whey that had received severe heat treatment did not, in most cases, elicit anaphylaxis when injected into animals that had been sensitized with unheated milk. Discrimination between antibodies of the IgG1 and IgG2 subclasses specific for beta-lactoglobulin showed that IgG1, the principal anaphylactic antibody in guinea-pigs, was preferentially depressed in animals drinking heat-denatured milk preparations. The results suggest that heat denaturation of whey protein may be a logical and simple strategy for producing a hypoallergenic baby milk. Nevertheless, the value of experiments in guinea-pigs for predicting results in man is uncertain and the proposal awaits assessment in clinical trials.

摘要

利用针对β-乳球蛋白、α-乳白蛋白、牛血清白蛋白、牛IgG1和α-酪蛋白的酶联免疫吸附测定法,测定了热变性牛奶乳清以及两种市售婴儿配方奶粉中的残留抗原蛋白。这种对抗原性的免疫化学评估与制剂在喂给豚鼠两周后使其产生免疫致敏的能力相关。测量抗体产生情况,并通过给动物静脉注射加热或未加热的牛奶蛋白来评估其对全身性过敏反应的易感性。在100℃或115℃加热30分钟的乳清蛋白发生了广泛变性,与巴氏杀菌乳清不同,它不能使豚鼠对过敏反应产生致敏作用。未检测到抗体产生或抗体产生水平非常低。SMA奶粉和SMA金装液体浓缩物中的蛋白质变性程度较小,按照制造商说明喂食这些配方奶粉的动物产生了相对较高水平的针对β-乳球蛋白和α-酪蛋白的抗体,并且大多数动物在静脉注射这些产品时出现了过敏反应。经过严重热处理的乳清不仅不能产生致敏作用,而且在大多数情况下,将其注射到用未加热牛奶致敏的动物体内时也不会引发过敏反应。对特异性针对β-乳球蛋白的IgG1和IgG2亚类抗体的区分表明,豚鼠体内主要的过敏反应抗体IgG1在饮用热变性牛奶制剂的动物中优先受到抑制。结果表明,乳清蛋白的热变性可能是生产低敏婴儿奶粉的一种合理且简单的策略。然而,在豚鼠身上进行的实验对于预测人类结果的价值尚不确定,该提议有待在临床试验中进行评估。

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