Division of Neuro and Inflammation Sciences, Department of Clinical and Experimental Medicine, Linköping University, Linköping, Sweden.
Department of Paediatrics, Department of Clinical and Experimental Medicine, Linköping University, Linköping, Sweden.
Sci Rep. 2020 Oct 30;10(1):18723. doi: 10.1038/s41598-020-75312-1.
Allergic diseases have become a major health problem, partly due to reduced microbial stimulation and a decreased dietary ω-3/ω-6 long-chain polyunsaturated fatty acid ratio. Prenatal exposures have been reported to influence allergy development, possibly induced via changes in maternal immune regulation. In a randomized double-blind placebo-controlled multicenter allergy prevention trial (PROOM-3), pregnant women were recruited at gestational week 20, and randomized to four study groups, one receiving both L. reuteri oil drops and ω-3 PUFA capsules (n = 22), the second receiving ω-3 PUFA supplementation and placebo regarding L. reuteri (n = 21), the third receiving L. reuteri and placebo regarding ω-3 PUFA (n = 22) and the fourth group receiving placebo capsules and placebo oil drops (n = 23). In this substudy, supplemental and pregnancy-related effects on maternal peripheral immune cell populations during pregnancy were assessed by flow cytometry immune phenotyping at gestational week 20, 32 and 4 days after delivery. The numbers of activated and regulatory T (Treg) cells (CD45RA Foxp3/CD45RAFoxp3) were reduced after delivery, with the lowest count in the L. reuteri supplemented group compared with the placebo group 4 days after delivery, while the ω-3 PUFA group did not differ from the placebo group. Several treatment-independent changes were observed during and after pregnancy in lymphocytes (CD4/8/19/56/45RA), CD1416 monocytes, and in subpopulations of T helper cells (Th) CD4CD45RATbet (Th1) and CD4CD45RARORC (Th17) cells. In conclusion, probiotic supplementation to the mother during the second half of pregnancy resulted in immunomodulatory effects among activated and resting Treg cells. Furthermore, several systemic immune modifying effects of pregnancy were observed.
过敏性疾病已成为一个主要的健康问题,部分原因是微生物刺激减少和饮食中 ω-3/ω-6 长链多不饱和脂肪酸比例降低。有报道称,产前暴露会影响过敏的发展,可能是通过改变母体免疫调节来诱导的。在一项随机、双盲、安慰剂对照的多中心过敏预防试验(PROOM-3)中,孕妇在妊娠 20 周时被招募,并随机分为四组研究,一组同时接受罗伊氏乳杆菌油滴和 ω-3PUFA 胶囊(n=22),第二组接受 ω-3PUFA 补充剂和安慰剂的罗伊氏乳杆菌(n=21),第三组接受罗伊氏乳杆菌和安慰剂的 ω-3PUFA(n=22),第四组接受安慰剂胶囊和安慰剂油滴(n=23)。在这项子研究中,通过流式细胞术免疫表型分析,在妊娠 20 周、32 周和产后 4 天评估补充剂和妊娠相关因素对孕妇外周免疫细胞群的影响。产后,活化和调节性 T(Treg)细胞(CD45RA Foxp3/CD45RAFoxp3)的数量减少,与产后 4 天的安慰剂组相比,罗伊氏乳杆菌补充组的数量最低,而 ω-3PUFA 组与安慰剂组没有差异。在妊娠期间和之后,观察到淋巴细胞(CD4/8/19/56/45RA)、CD1416 单核细胞和 T 辅助细胞(Th)CD4CD45RATbet(Th1)和 CD4CD45RARORC(Th17)细胞亚群的几个与治疗无关的变化。总之,在妊娠后半期给母亲补充益生菌会导致活化和静止的 Treg 细胞产生免疫调节作用。此外,还观察到妊娠的几个全身性免疫调节作用。