Department of Immunology and Food Microbiology, Institute of Animal Reproduction and Food Research of the Polish Academy of Sciences, Tuwima 10 Str., 10-748 Olsztyn, Poland.
Department of Public Health, Faculty of Health Sciences, Collegium Medicum, University of Warmia and Mazury, 10-082 Olsztyn, Poland.
Nutrients. 2021 Jan 25;13(2):349. doi: 10.3390/nu13020349.
The presence of various proteins, including modified ones, in food which exhibit diverse immunogenic and sensitizing properties increases the difficulty of predicting host immune responses. Still, there is a lack of sufficiently reliable and comparable data and research models describing allergens in dietary matrices. The aim of the study was to estimate the immunomodulatory effects of β-lactoglobulin (β-lg) in comparison to those elicited by κ-casein (κ-CN), in vivo and ex vivo, using naïve splenocytes and a mouse sensitization model. Our results revealed that the humoral and cellular responses triggered by β-lg and κ-CN were of diverse magnitudes and showed different dynamics in the induction of control mechanisms. β-Lg turned out to be more immunogenic and induced a more dominant Th1 response than κ-CN, which triggered a significantly higher IgE response. For both proteins, CD4 lymphocyte profiles correlated with CD4CD25 and CD4CD25Foxp3 T cells induction and interleukin 10 secretion, but β-lg induced more CD4CD25Foxp3 Tregs. Moreover, ex vivo studies showed the risk of interaction of immune responses to different milk proteins, which may exacerbate allergy, especially the one caused by β-lg. In conclusion, the applied model of in vivo and ex vivo exposure to β-lg and κ-CN showed significant differences in immunoreactivity of the tested proteins (κ-CN demonstrated stronger allergenic potential than β-lg), and may be useful for the estimation of allergenic potential of various food proteins, including those modified in technological processes.
各种蛋白质的存在,包括修饰后的蛋白质,这些蛋白质在食物中表现出不同的免疫原性和致敏特性,增加了预测宿主免疫反应的难度。尽管如此,目前仍然缺乏足够可靠和可比的数据和研究模型来描述膳食基质中的过敏原。本研究的目的是评估β-乳球蛋白(β-lg)与κ-酪蛋白(κ-CN)的体内和体外免疫调节作用,使用幼稚脾细胞和小鼠致敏模型。我们的结果表明,β-lg 和 κ-CN 引发的体液和细胞反应在诱导控制机制方面具有不同的强度和不同的动力学。β-lg 比 κ-CN 更具免疫原性,并诱导更占主导地位的 Th1 反应,而 κ-CN 则引发更高的 IgE 反应。对于这两种蛋白质,CD4 淋巴细胞谱与 CD4CD25 和 CD4CD25Foxp3 T 细胞的诱导和白细胞介素 10 的分泌相关,但β-lg 诱导更多的 CD4CD25Foxp3 Treg。此外,体外研究表明,不同乳蛋白的免疫反应相互作用的风险,这可能会加重过敏,尤其是β-lg 引起的过敏。总之,应用β-lg 和 κ-CN 的体内和体外暴露模型显示出测试蛋白的免疫反应性存在显著差异(κ-CN 比 β-lg 具有更强的变应原性潜力),并且可能有助于评估包括在加工过程中修饰的各种食物蛋白的变应原性潜力。