Hall Lindsay S, Hall Andrew M, Pickford Wendy, Vickers Mark A, Urbaniak Stanislaw J, Barker Robert N
Haematologica. 2014 Mar;99(3):588-96. doi: 10.3324/haematol.2012.082081. Epub 2014 Jan 17.
The offspring from pregnancies of women who have developed anti-D blood group antibodies are at risk of hemolytic disease of the newborn. We have previously mapped four peptides containing immunodominant T-helper cell epitopes from the RhD protein and the purpose of the work was to develop these into a product for suppression of established anti-D responses. A panel of each of the four immunodominant RhD peptides was synthesized with modifications to improve manufacturability and solubility, and screened for retention of recognition by human T-helper cells. A selected version of each sequence was combined in a mixture (RhDPmix), which was tested for suppressive ability in a humanized murine model of established immune responses to RhD protein. After HLA-DR15 transgenic mice had been immunized with RhD protein, a single dose of RhDPmix, given either intranasally (P=0.008, Mann-Whitney rank sum test) or subcutaneously (P=0.043), rapidly and significantly suppressed the ongoing antibody response. This was accompanied by reduced T-helper cell responsiveness, although this change was less marked for subcutaneous RhDPmix delivery, and by the recruitment of cells with a regulatory T-cell phenotype. The results support human trials of RhDPmix peptide immunotherapy in women with established antibody responses to the RhD blood group.
已产生抗-D血型抗体的女性所孕育的后代有患新生儿溶血病的风险。我们之前已绘制出四种含有来自RhD蛋白的免疫显性辅助性T细胞表位的肽段,本研究的目的是将这些肽段开发成一种产品,用于抑制已有的抗-D反应。合成了一组四种免疫显性RhD肽段,并进行了修饰以提高可制造性和溶解性,然后筛选其是否能被人辅助性T细胞识别。每个序列的选定版本混合在一起(RhDPmix),在已建立对RhD蛋白免疫反应的人源化小鼠模型中测试其抑制能力。用RhD蛋白免疫HLA-DR15转基因小鼠后,单剂量的RhDPmix经鼻内给药(P = 0.008,曼-惠特尼秩和检验)或皮下给药(P = 0.043),能迅速且显著地抑制正在进行的抗体反应。这伴随着辅助性T细胞反应性降低,不过皮下注射RhDPmix时这种变化不太明显,同时还伴随着具有调节性T细胞表型的细胞募集。这些结果支持对已产生针对RhD血型抗体反应的女性进行RhDPmix肽免疫疗法的人体试验。