van den Boogaardt Daniëlle E M, van Miert Paula P M C, Koekkoek Karin M, de Vaal Yvonne J H, van Rood Jon J, Claas Frans H J, Roelen Dave L
Department of Immunohematology and Blood Transfusion, Leiden University Medical Center, P.O. Box 9600, 2300 RC Leiden, The Netherlands.
Hum Immunol. 2005 Dec;66(12):1203-12. doi: 10.1016/j.humimm.2005.12.002. Epub 2006 Mar 24.
Pre- and/or perinatal exposure to noninherited maternal HLA antigens (NIMA) is associated with a decreased HLA antibody formation against the NIMA and a significantly better graft survival of kidney grafts from siblings or those from unrelated donors who were mismatched for the NIMA haplotype compared with the NIPA (noninherited paternal HLA antigens) haplotype later in life. These observations suggest that some form of immunological tolerance against NIMA is induced. We analyzed the in vitro T cell reactivity of healthy individuals toward their parents and/or siblings expressing the NIMA or NIPA haplotype to explore whether the alloimmune response to NIMA has distinct characteristics compared with NIPA. No differences were detected by mixed lymphocyte reactions (MLR) and supernatants taken from the MLR showed no differences in IFN-gamma and IL-10 production. Additionally, no differences were found with IFN-gamma and IL-10 Elispot analyses. Phenotypic analysis revealed no selective increase in the number of CD3-CD8dim cells (thought to be a NK-like regulator cell) and the number of CD4+CD25+CD152+ cells (naturally occurring regulatory T cells) after stimulation with NIMA-expressing cells when compared with NIPA-expressing cells. In conclusion, no evidence of an influence of a NIMA effect on the cellular level was found in healthy individuals with "standard" immunological techniques.
产前和/或围产期暴露于非遗传的母体HLA抗原(NIMA)与针对NIMA的HLA抗体形成减少相关,并且与那些在生命后期具有NIPA(非遗传的父体HLA抗原)单倍型错配的同胞或无关供体的肾移植相比,具有NIMA单倍型错配的肾移植的移植物存活明显更好。这些观察结果表明诱导了某种形式的针对NIMA的免疫耐受。我们分析了健康个体对表达NIMA或NIPA单倍型的父母和/或同胞的体外T细胞反应性,以探讨与NIPA相比,对NIMA的同种免疫反应是否具有独特特征。通过混合淋巴细胞反应(MLR)未检测到差异,并且从MLR中获取的上清液在IFN-γ和IL-10产生方面没有差异。此外,IFN-γ和IL-10酶联免疫斑点分析也未发现差异。表型分析显示,与表达NIPA的细胞相比,在用表达NIMA的细胞刺激后,CD3-CD8dim细胞(被认为是一种NK样调节细胞)和CD4 + CD25 + CD152 +细胞(天然存在的调节性T细胞)的数量没有选择性增加。总之,在采用“标准”免疫技术的健康个体中,未发现NIMA效应在细胞水平上有影响的证据。