Demers-Mathieu Veronique, Underwood Mark A, Beverly Robert L, Dallas David C
Nutrition Program, School of Biological and Population Health Sciences, College of Public Health and Human Sciences, Oregon State University, Corvallis, Oregon, USA.
Department of Pediatrics, University of California, Sacramento, California, USA.
Neonatology. 2018;114(3):242-250. doi: 10.1159/000489387. Epub 2018 Jun 25.
Human milk immunoglobulins (Ig) are an important support for the naïve infant immune system; yet the extent to which these proteins survive within the infant digestive tract, particularly for preterm infants, is poorly studied.
Our objective was to evaluate the survival of human milk Igs in the preterm stomach across postprandial time.
Human milk and infant gastric samples were collected from 11 preterm (23-32 weeks gestational age) mother-infant pairs within 7-98 days postnatal age. Preterm gastric samples were collected 1, 2, and 3 h after the beginning of the feeding. Samples were analyzed for concentration of total IgA (secretory IgA [SIgA]/IgA), total secretory component (SC/SIgA/SIgM), total IgM (SIgM/IgM), and IgG via enzyme-linked immunosorbent assay. Ig-chain fragment peptides were determined using peptidomic analysis. One-way analysis of variance with repeated measures followed by Tukey's multiple comparison tests was applied.
Concentrations of total IgA were lower in the gastric contents at 3 h postprandial compared with human milk and gastric contents at 1 and 2 h. Human milk SC/SIgA/SIgM, IgG, and total IgM concentrations remained stable in the preterm stomach across postprandial time. Peptide counts from the Ig alpha-chain and the Ig gamma-chain increased in gastric contents from 1 to 2 h postprandial. Peptide counts from the human milk Ig-chain, Ig-chain, and SC were stable across postprandial time. These peptides from Ig-chains were not present in human milk but were released in the stomach due to their partial degradation.
Human milk total SC (SIgA/SC/SIgM), total IgM, and IgG survived mostly intact through the preterm infant stomach, while total IgA was -partially digested.
人乳免疫球蛋白(Ig)是初生人婴儿免疫系统的重要支持;然而,这些蛋白质在婴儿消化道内的存活程度,尤其是对早产儿而言,研究较少。
我们的目的是评估人乳Ig在早产儿胃内餐后不同时间的存活情况。
从11对早产(胎龄23 - 32周)母婴对中收集产后7 - 98天内的人乳和婴儿胃样本。在喂养开始后1、2和3小时收集早产儿胃样本。通过酶联免疫吸附测定法分析样本中总IgA(分泌型IgA[SIgA]/IgA)、总分泌成分(SC/SIgA/SIgM)、总IgM(SIgM/IgM)和IgG的浓度。使用肽组学分析确定Ig链片段肽。应用重复测量的单因素方差分析,随后进行Tukey多重比较检验。
与母乳以及餐后1小时和2小时的胃内容物相比,餐后3小时胃内容物中总IgA浓度较低。母乳中SC/SIgA/SIgM、IgG和总IgM浓度在早产儿胃内餐后不同时间保持稳定。餐后1至2小时胃内容物中Igα链和Igγ链的肽计数增加。母乳Ig链、Ig链和SC的肽计数在餐后不同时间保持稳定。这些来自Ig链的肽在母乳中不存在,但由于部分降解而在胃中释放。
人乳总SC(SIgA/SC/SIgM)、总IgM和IgG在早产儿胃内大多完整存活,而总IgA被部分消化。