首页> 美国卫生研究院文献>Immunology >The interaction of infant formula with macrophages: effect on phagocytic activity relationship to expression of class II MHC antigen and survival of orally administered macrophages in the neonatal gut.
【2h】

The interaction of infant formula with macrophages: effect on phagocytic activity relationship to expression of class II MHC antigen and survival of orally administered macrophages in the neonatal gut.

机译:婴儿配方食品与巨噬细胞的相互作用:对吞噬活性的影响与II类MHC抗原表达的关系以及新生儿肠道中口服巨噬细胞的存活率。

代理获取
本网站仅为用户提供外文OA文献查询和代理获取服务,本网站没有原文。下单后我们将采用程序或人工为您竭诚获取高质量的原文,但由于OA文献来源多样且变更频繁,仍可能出现获取不到、文献不完整或与标题不符等情况,如果获取不到我们将提供退款服务。请知悉。

摘要

The effect of infant formula on human peritoneal and breast milk macrophages has been investigated. The ability of peritoneal macrophages to subsequently ingest and degrade immune complexes was slightly impaired, but breast milk cells were not affected. However, the cells were found to have bound antigenically intact casein and beta-lactoglobulin, although little, if any, alpha-lactalbumin was bound. Furthermore, a positive correlation was found between binding of these proteins and expression of HLA-DR antigen. Labelled macrophages fed to newborn mice survived for at least 4 hr in the gastrointestinal tract and, in some cases, localized in the mucosal tissue. In one case a labelled cell was found in the spleen. These findings indicate that breast milk macrophages may be able to perform immunological functions in the gut, and suggest that binding of cows' milk proteins by macrophages may constitute a first step in the sensitization of the neonate to cow's milk proteins. Human milk macrophages may also play a protective role by acting as antigen-presenting cells in the local immune response of the gut.
机译:已经研究了婴儿配方食品对人腹膜和母乳巨噬细胞的影响。腹膜巨噬细胞随后摄取和降解免疫复合物的能力略有受损,但母乳细胞未受影响。然而,发现细胞结合了抗原完整的酪蛋白和β-乳球蛋白,尽管很少(如果有的话)结合α-乳白蛋白。此外,在这些蛋白的结合与HLA-DR抗原的表达之间发现正相关。喂养新生小鼠的标记巨噬细胞在胃肠道中存活了至少4个小时,在某些情况下还位于粘膜组织中。在一种情况下,在脾脏中发现了标记细胞。这些发现表明,母乳巨噬细胞可能能够在肠道中发挥免疫功能,并表明巨噬细胞与牛乳蛋白的结合可能构成了新生儿对牛乳蛋白致敏的第一步。人乳巨噬细胞还可以通过在肠道的局部免疫反应中充当抗原呈递细胞来发挥保护作用。

著录项

相似文献

  • 外文文献
  • 中文文献
  • 专利
代理获取

客服邮箱:kefu@zhangqiaokeyan.com

京公网安备:11010802029741号 ICP备案号:京ICP备15016152号-6 六维联合信息科技 (北京) 有限公司©版权所有
  • 客服微信

  • 服务号